trimethylamine borane

Trimethylamine borane structural formula

Structural formula

Business number 01J7
Molecular formula C3H12BN
Molecular weight 72.95
label

Trimethylaminoboron,

triphenylphosphine borane,

Borane Trimethylamine Complex,

Borane-trimethylamine Complex,

Trimethylamine borane,

(CH3)3N·BH3

Numbering system

CAS number:75-22-9

MDL number:MFCD00012420

EINECS number:200-850-4

RTECS number:PA0525000

BRN number:3905060

PubChem number:24849578

Physical property data


1. Character:Crystal. Sensitive to moisture. solid in100Stable.


2.Density (g/mL,25/4): Undetermined


3. Relative vapor density ( g/mL,AIR =1): Undetermined


4. Melting point (ºC): 94


5. Boiling point (ºC,Normal pressure):72


6. Boiling point (ºC,5.2kPa): Undetermined


7. Refractive index: Undetermined


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation ( º): Undetermined


10. Autoignition point or ignition temperature (ºC): Undetermined


11. Vapor pressure (kPa,25ºC): Undetermined


12. Saturated vapor pressure (kPa,60ºC ): Undetermined


13. Heat of combustion (KJ/mol): Undetermined


14. Critical temperature (ºC): Undetermined


15. Critical Pressure (KPa): Undetermined


16. Oil and water (octanol /Log value of the partition coefficient of water: Undetermined


17.   Explosion limit (%,V/V): Undetermined


18. Lower explosion limit (%,V/V): Undetermined


19. Solubility: Undetermined.


Toxicological data

1, acute toxicity


Mouse abdominal cavityLD50: 175mg/kg


Mouse abdominal cavityLD50:140mg/kg


2. Teratogenicity


Mouse: 10umol/L


E. coli: 10umol/plate

Ecological data

None yet

Molecular structure data

None yet

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP):


2. Number of hydrogen bond donors:0


3. Number of hydrogen bond acceptors:0


4. Number of rotatable chemical bonds:0


5. Number of tautomers:


6. Topological molecule polar surface area (TPSA):0


7. Number of heavy atoms:5


8. Surface charge:1


9. Complexity:28.4


10. Number of isotope atoms:0


11. Determine the number of atomic stereocenters:0


12. Uncertain number of atomic stereocenters:0


13. Determine the number of stereocenters of chemical bonds:0


14. Uncertain number of chemical bond stereocenters:0


15. Number of covalent bond units:1

Properties and stability

Storage method

This product should be inert Gas-sealed and stored in a cool and dry place.

Synthesis method

None yet

Purpose

Keto and Schiff Bases (Schiff bases) reduction and hydroboration of alkenes. Exchange with acidic deuterium oxide to prepare deuterated reduced compounds.

extended-reading:https://www.newtopchem.com/archives/44867
extended-reading:https://www.newtopchem.com/archives/40065
extended-reading:https://www.newtopchem.com/archives/44965
extended-reading:https://www.morpholine.org/category/morpholine/page/2/
extended-reading:https://www.cyclohexylamine.net/catalyst-sa-1-polyurethane-catalyst-sa-1/
extended-reading:https://www.morpholine.org/elastomer-environmental-protection-catalyst-environmental-protection-catalyst/
extended-reading:https://www.newtopchem.com/archives/44368
extended-reading:https://www.morpholine.org/bis3-dimethylaminopropylamino-2-propanol/
extended-reading:https://www.newtopchem.com/archives/1915
extended-reading:https://www.cyclohexylamine.net/category/product/page/35/

Histamine dihydrochloride

Histamine dihydrochloride structural formula

Structural formula

Business number 0185
Molecular formula C5H9N3•2HCl
Molecular weight 184.07
label

2-(4-Imidazolyl)ethylamine hydrochloride,

2-(4-Imidazolyl)ethylamine dihydrochloride

Numbering system

CAS number:56-92-8

MDL number:MFCD00012703

EINECS number:200-298-4

RTECS number:MS1575000

BRN number:3624116

PubChem number:24277777

Physical property data

1. Characteristics: colorless Prismatic crystal or white crystalline powder. Odorless. Has a salty taste. Sensitive to light and air. Hygroscopic.


2. Density (g/mL,25/4℃) : Undetermined


3.  Relative vapor density (g/mL,AIR=1): Undetermined


4. Melting point (ºC): 244246


5. Boiling point (ºC,Normal pressure): Undetermined


6. Boiling point (ºC,5.2kPa): Undetermined


7. Refractive index:��OK


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation ( º): Undetermined


10. Spontaneous ignition point or ignition Combustion temperature (ºC): not OK


11. Vapor Pressure (kPa,25ºC): Undetermined


12. Saturated vapor pressure ( kPa,60ºC): Undetermined


13. Heat of combustion (KJ/mol): Undetermined


14. Critical temperature (ºC): Undetermined


15. Critical Pressure (KPa): Undetermined


16. Oil and water (octanol /Water) partition coefficient pair Value: Undetermined


17. Explosion upper limit (%,V/V): Undetermined


18. Lower explosion limit (%,V/V): not OK


19. Solubility: Easy Soluble in water, methanol, ethanol and acetone, very slightly soluble in ether and chloroform. Aqueous solutions are acidic to litmus

Toxicological data

1, acute toxicity: rat abdominal cavity LD50: 1550mg/kg; rat via brain LD50: >28mg/kg; mouse Oral LD50: 2534mg/kg; mouse abdominal cavity LD50: 184mg/kg;
Mouse subcutaneous LDLo: 1300mg/kg; Mouse intravenous LD50: 370mg/kg; Rabbit intravenous LD50: 200mg/ kg; Guinea pig abdominal cavity LD50: 4602ug/kg;
Guinea pig parenteral LD50: 570ug/kg
2, reproductive toxicity: abdominal cavity of female mice TDLo: 2400mg/kg, 1-6 days after conception

Ecological data

None yet

Molecular structure data

1. Molar refractive index:31.86


2. Molar volume (m3/mol):97.4


3. isotonic specific volume (90.2K):266.6


4. Surface Tension (dyne/cm):56.0


5. Polarizability10-24cm3<SPAN style="FONT-SIZE: 9pt; FONT-FAMILY: Song Dynasty; mso-asci

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 4

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 2

6. Topological molecule polar surface area 54.7

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 64.7

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 3

Properties and stability

None yet

Storage method

This product should be sealed and stored in a dry and dark place.

Synthesis method

None yet

Purpose

Biochemical studies, determination of histamine substrates.

extended-reading:https://www.bdmaee.net/dabco-t-12-catalyst-cas280-57-9-evonik-germany/
extended-reading:https://www.newtopchem.com/archives/45071
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/28.jpg
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/102.jpg
extended-reading:https://www.morpholine.org/pc-cat-tka-polyurethane-metal-carboxylate-catalyst-polycat-46/
extended-reading:https://www.cyclohexylamine.net/category/product/page/8/
extended-reading:https://www.bdmaee.net/niax-ef-600-low-odor-balanced-tertiary-amine-catalyst-momentive/
extended-reading:https://www.bdmaee.net/pc-cat-pmdeta-catalyst-pentamethyldiethylenetriamine/
extended-reading:https://www.cyclohexylamine.net/2-2-aminoethylaminoethanol/
extended-reading:https://www.bdmaee.net/dibutyloxostannane/

o-aminoazotoluene

Ortho-aminoazotoluene structural formula

Structural formula

Business number 02CC
Molecular formula C14H15N3
Molecular weight 255.29
label

4-amino-2‘,3-dimethylazobenzene,

Toluene azoaminotoluene,

2,3′-dimethyl-4′-aminoazobenzene,

o-Aminoazotoluene,

Solvent yellow 3,

2,3-Dimethyl-4′-aminoazobenzene,

Fast garnet GBS base,

2-Methyl-4-[(2-methylpentyl)azo]benzenamine,

Solvent yellow35-(o-Tolylazo)-2-aminnotoluene

Numbering system

CAS number:97-56-3

MDL number:MFCD00007733

EINECS number:202-591-2

RTECS number:XU8800000

BRN number:6506005

PubChem number:24847463

Physical property data

  1. Appearance: yellow-brown powder.
  2. Density (g/mL, 20℃): Undetermined
  3. Relative vapor density (g/mL, air=1): Undetermined
  4. Melting point ( ºC): 101~102
  5. Boiling point (ºC, normal pressure): Undetermined
  6. Boiling point (ºC, KPa): Undetermined
  7. Refractive index: Undetermined Determined
  8. Flash point (ºC): Not determined
  9. Specific optical rotation (º): Not determined
  10. Autoignition point or ignition temperature (ºC): Not determined Determined
  11. Vapor pressure (mmHg, ºC): Undetermined
  12. Saturation vapor pressure (kPa, ºC): Undetermined
  13. Heat of combustion (KJ/mol) : Undetermined
  14. Critical temperature (ºC): Undetermined
  15. Critical pressure (KPa): Undetermined
  16. Oil-water (octanol/water) partition coefficient Log value: Undetermined
  17. Upper explosion limit (%, V/V): Undetermined
  18. Lower explosion limit (%, V/V): Undetermined
  19. Solubility: insoluble in water, soluble in ethanol, chloroform, and ether.

Toxicological data

1. Acute toxicity: Rat oral LD5O: 1500 mg/kg N02

Ecological data

This substance is harmful to the environment. Do not let this substance enter the environment.

Molecular structure data

1. Molar refractive index: 69.61

2. Molar volume (cm3/mol): 205.4

3. Isotonic specific volume (90.2K ): 516.9

4. Surface tension (dyne/cm): 40.0

5. Polarizability (10-24cm3): 27.59

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 3.7

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 2

6. Topological molecule polar surface area 50.7

7. Number of heavy atoms: 17

8. Surface charge: 0

9. Complexity: 264

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters��: 0

12. Uncertain number of stereocenters of atoms: 0

13. Determined number of stereocenters of chemical bonds: 0

14. Uncertain Number of stereocenters of chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

1. Avoid contact with strong oxidants.

2. May cause cancer, avoid exposure.

Storage method

1. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. The packaging is sealed. should be kept away from oxidizer, do not store together. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills.

Synthesis method

None yet

Purpose

1. Used as dyes and pharmaceutical intermediates.

extended-reading:https://www.morpholine.org/n-methylimidazole/
extended-reading:https://www.cyclohexylamine.net/ethyl-4-bromobutyrate/
extended-reading:https://www.bdmaee.net/efficient-trimerization-catalyst-for-aliphatic-and-alicyclic-isocyanates/
extended-reading:https://www.bdmaee.net/toyocat-et-catalyst-tosoh/
extended-reading:https://www.cyclohexylamine.net/sponge-foaming-catalyst-smp-low-density-sponge-catalyst-smp/
extended-reading:https://www.bdmaee.net/tegoamin-dmea-catalyst-cas108-01-0-degussa-ag/
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/31.jpg
extended-reading:https://www.bdmaee.net/cas-108-01-0-2/
extended-reading:https://www.newtopchem.com/archives/44322
extended-reading:https://www.cyclohexylamine.net/synthesis-of-low-free-tdi-trimer/

4-Aminomethylbenzoic acid

4-aminomethylbenzoic acid structural formula

Structural formula

Business number 0184
Molecular formula C8H9NO2
Molecular weight 151.17
label

p-aminomethylbenzoic acid

Numbering system

CAS number:56-91-7

MDL number:MFCD00010203

EINECS number:200-297-9

RTECS number:None

BRN number:1100606

PubChem number:24846170

Physical property data

1. Character: Hydrate It is white scaly or crystalline powder. Odorless, slightly bitter taste.


2. Density (g/mL,25/4℃) : Undetermined


3. Relative vapor density (g/mL,AIR=1): Undetermined


4. Melting point (ºC): 340-350


5. Boiling point (ºC,Normal pressure): Undetermined


6. Boiling point (ºC,5.2kPa): Undetermined


7. Refractive index: not OK


8. Flash point (ºC): Undetermined


9. Specific optical rotation ( º): Undetermined


10. Spontaneous ignition point or ignition Combustion temperature (ºC): not OK


11. Vapor Pressure (kPa,25ºC): Undetermined


12. Saturated vapor pressure ( kPa,60ºC): Undetermined


13. Heat of combustion (KJ/mol): Undetermined


14. Critical temperature (ºC): Undetermined


15. Critical Pressure (KPa): Undetermined


16. Oil and water (octanol /Water) partition coefficient pair Value: Undetermined


17. Explosion upper limit (%,V/V): not OK


18. Lower explosion limit (%,V/V): Undetermined


19. Solubility: soluble In boiling water, slightly soluble in water, almost insoluble in ethanol, benzene and chloroform.

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

5. Molecular property data:


1. Molar refractive index: 41.63


2. Molar volume (m3/mol):121.9


3. isotonic specific volume (90.2K):335.2


4. Surface tension (dyne/cm):57.1


5. Polarizability10-24cm3):16.50

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: none

6. Topological molecule polar surface area 63.3

7. Number of heavy atoms: 11

8. Surface charge: 0

9. Complexity: 139

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None yet

Storage method

This product should be kept sealed.

Synthesis method

There are three processes: (1) is derived from the catalytic hydrogenation of p-cyanobenzoic acid; (2) aminated from p-chloromethylbenzoic acid And get; (3) is derived from the amination of p-bromomethylbenzoic acid.

Purpose

Organic synthesis intermediates. Hemostatic drugs and fibrinolytic inhibitors are suitable for various diseases caused by excessive fibrinolytic enzyme activity.

extended-reading:https://www.newtopchem.com/archives/category/products/page/40
extended-reading:https://www.bdmaee.net/fascat4400-tertiary-amine-catalyst-arkema-pmc/
extended-reading:https://www.bdmaee.net/nt-cat-a-4-catalyst-cas8001-28-0-newtopchem/
extended-reading:https://www.bdmaee.net/dabco-ne300-dabco-foaming-catalyst-polyurethane-foaming-catalyst-ne300/
extended-reading:https://www.morpholine.org/efficient-reaction-type-equilibrium-catalyst-reactive-equilibrium-catalyst/
extended-reading:https://www.newtopchem.com/archives/39736
extended-reading:https://www.newtopchem.com/archives/category/products/page/107
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/Polyurethane-rigid-foam-catalyst-CAS-15875-13-5-catalyst-PC41.pdf
extended-reading:https://www.newtopchem.com/archives/40032
extended-reading:https://www.cyclohexylamine.net/2-2-dimethylaminoethylmethylamino-ethanol-nnn-trimethylaminoethylethanolamine/

calcium carbide

Calcium carbide structural formula

Structural formula

Business number 01J6
Molecular formula CaC2
Molecular weight 64.10
label

Carbide Level 4,

calcium carbide,

Calcium acetylide,

Acetylenogen,

other

Numbering system

CAS number:75-20-7

MDL number:MFCD00010905

EINECS number:200-848-3

RTECS number:None

BRN number:3909011

PubChem number:24856368

Physical property data

1. Characteristics: Colorless crystals, industrial products are gray-black lumps, and the cross-section is purple or gray. [1]

2. Melting point (℃): 2300[2]

3. Boiling point (℃): decomposition [3]

4. Relative density (water = 1): 2.22[4]

5. Octanol/ Water distribution coefficient: -0.30[5]

6. Ignition temperature (℃): >325[6]

7.Solubility: No data yet

Toxicological data

1. Acute toxicity No data available

2. Irritation No data available

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3 .Non-biodegradability No information available

4. Other harmful effects[7] This substance is harmful to the environment and should be specially Pay attention to water pollution.

Molecular structure data

None yet

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 8

5. Number of tautomers: none

6. Topological molecule polar surface area 61.8

7. Number of heavy atoms: 18

8. Surface charge: 0

9. Complexity: 271

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Stability[8] Stable

2. Incompatible substances[9] Water, alcohols, acids

3. Conditions to avoid contact[10] Humid air

4. Hazards of aggregation[11] No aggregation

Storage method

Storage Precautions[12] Store in a cool, dry and well-ventilated special warehouse with a temperature not exceeding 32°C and a relative humidity not exceeding 75%. Keep away from fire and heat sources. The packaging must be sealed and protected from moisture. It should be stored separately from acids, alcohols, etc. and avoid mixed storage. The storage area should be equipped with appropriate� materials to contain spills.

Synthesis method

1. The electric furnace reduction method is currently the only method for industrial production of calcium carbide. This method was industrialized in the United States as early as 1895. The production involves high-temperature operations, a lot of dust, and high power consumption. Improvements in the process can improve operating conditions, reduce heat loss, and increase carbon monoxide recovery and utilization. Closed and large-scale Calcium carbide furnace. Crush the coke and lime, mix them evenly according to the proportion, add them to a closed calcium carbide furnace, heat them with electricity, and perform a reduction reaction at 2000-2200°C to generate molten calcium carbide, which flows from the furnace into a calcium carbide pot for cooling, crushing, and packaging. kg/ton of coke (84% fixed carbon) 550 limestone (CaO92%) 840 electrode paste 30 electricity 3200 (degree/ton)

2. Calcium carbide can be directly produced from the two elements of carbon and metallic calcium in an electric arc furnace Synthetically, or by reacting calcium oxide and carbon in an electric arc furnace at a high temperature of 2000°C. The purity of the products produced by these two methods is not high. The purity of calcium carbide produced by heating calcium cyanamide CaCN2 or calcium cyanamide and carbon in high vacuum can reach 99%.

The alumina boat is filled with pure calcium cyanamide or a mixture of calcium cyanamide and acetylene carbon black (or sugar charcoal), and the boat is placed in a ground-mouthed high-aluminum vessel with one end closed. To make porcelain tubes, this tube is connected to a vacuum pump and heated with a molybdenum wire furnace.

Heating CaCN2 or the mixture of CaCN2 and C must be carried out in two steps: the first step is to heat to 1100~1150℃ for 2~3 hours in high vacuum to fully decompose CaCN2 and remove as much N2 as possible. At this time, care should be taken to control the temperature not to exceed 1150°C to avoid the formation of a CaCN2CaC2 eutectic at 1170°C. In the second step, continue to raise the temperature to 1350°C for 1 hour, remove the remaining N2, and obtain pure white calcium carbide. Purity reaches 99%.

Attached is the preparation method of calcium cyanamide. Pure HCN is dried by CaCl2 and P2O5 and condensed in a low-temperature receiver. The collection amount should be equal to 3 times the calculated amount. Put CaCO3 in a porcelain boat, place the porcelain boat in a porcelain tube, and heat the porcelain tube to 700~850°C. Then warm the HCN receiver to 18°C. N2 gas mixed with a small amount of NH3 is used to carry HCN through CaCO3, and pure white CaCN2 can be obtained after 3 hours, with a purity of 99.4%.

Purpose

1. About 60% of calcium carbide is used in chemical production, and the remaining 40% is used in metal welding and cutting. A series of chemical products can be produced using calcium carbide as raw materials, such as PVC resin, polyvinyl alcohol, vinyl acetate, chloroprene rubber, butanol, octanol, tricyanethylene, tetracyanoethylene, acetaldehyde, acetylene carbon black, lime nitrogen, etc. . The largest consumption is the production of PVC resin, accounting for 60% of the consumption of calcium carbide for chemical industry. Calcium carbide powder is irritating and can damage the skin and respiratory system.

2. It is an important basic chemical raw material, mainly used to produce acetylene gas and calcium cyanamide. Also used in organic synthesis, etc. [13]

extended-reading:https://www.bdmaee.net/wp-content/uploads/2016/06/Jeffcat-ZF-22-MSDS.pdf
extended-reading:https://www.newtopchem.com/archives/1081
extended-reading:https://www.newtopchem.com/archives/40267
extended-reading:https://www.newtopchem.com/archives/45149
extended-reading:https://www.bdmaee.net/wp-content/uploads/2016/06/Tegoamin-BDE.pdf
extended-reading:https://www.bdmaee.net/pc-cat-tka30-catalyst-nitro/
extended-reading:https://www.bdmaee.net/polyurethane-monosodium-glutamate/
extended-reading:https://www.bdmaee.net/tmr-4-dabco-tmr-4-trimer-catalyst-tmr-4/
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/Dioctyl-dimaleate-di-n-octyl-tin-CAS33568-99-9-Dioctyl-dimaleate-di-n-octyl-tin.pdf
extended-reading:https://www.cyclohexylamine.net/category/product/page/33/

L-cystine

L-cystine structural formula

Structural formula

Business number 0183
Molecular formula C6H12N2O4S2
Molecular weight 240.3
label

(R,R)-3,3′-dithiobis(2-aminopropionic acid),

Dithioaminopropionic acid,

Bis-beta-thioalanine,

disulfidealanine,

(R,R)-3,3′-Dithiobis(2-aminopropionicacid),

Cystine,

L-Dicysteine,

(R,R)-(-)Cystine,

L-cystinic acid,

biochemical reagents,

intermediates,

amino acids

Numbering system

CAS number:56-89-3

MDL number:MFCD00064228

EINECS number:200-296-3

RTECS number:HA2690000

BRN number:1728094

PubChem number:24893101

Physical property data

1. Properties: White hexagonal plate-shaped crystals or crystalline powder. Odorless and tasteless.

2. Density (g/mL, 25/4℃): 1.677

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): point 260~261℃ (decomposition)

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºC): Not determined

9. Specific rotation (º): [α]D20 -223.4° (C=1, in 1mol/L hydrochloric acid).

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturation Vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (% ,V/V): Undetermined

18. Lower explosion limit (%,V/V): Undetermined

19. Solubility: Soluble in dilute acid and alkaline solutions, Very slightly soluble in water, insoluble in ethanol, ether, benzene and chloroform.

Toxicological data

1. Acute toxicity: Rat oral LD50: 25mg/kg2.Other multiple dose toxicity: rat oral TDLo: 279mg/kg/93D-C

Ecological data

None yet

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 55.95

2. Molar volume (cm3/mol): 152.8

3. Isotonic specific volume (90.2K): 468.6

4. Surface tension (dyne/cm): 88.2

5. Polarizability (10-24cm3): 22.18

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -6.3

2. Number of hydrogen bond donors: 4

3. Number of hydrogen bond acceptors: 8

p>

4. Number of rotatable chemical bonds: 7

5. Number of tautomers: none

6. Topological molecule polar surface area 177

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 192

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 2

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Stable properties under normal temperature and pressure.

2. Found in tobacco leaves.

3. Widely found in hair, hair, bones and horns.

4. There are three isomers: left-handed body, right-handed body and racemate.

Storage method

This product should be sealed and stored in a cool, dry place away from light.

Synthesis method

1. L-cystine was discovered in 1810 by Wollaston from bladder stones. In 1832, Berzelius named it cystine. It is a sulfur-containing amino acid that exists in small amounts in proteins, mostly in the keratin of hair, fingers and claws. It can also be obtained synthetically. Industrially extracted from hair, the yield can reach 7.5-8%. In actual production, some only reach 5%.
2.Hydrolyze pig hair in hydrochloric acid, filter to remove impurities, crystallize to obtain crude product, add activated carbon for decolorization and decolorizationPrepared from iron, washing and drying.

3.

Add 720kg of hydrochloric acid with a concentration of 10mol/L into the hydrolysis tank and heat it to 70~80℃. Quickly add 400kg of human hair or pig, continue to heat to 100℃, and raise the temperature to 110~117℃ within 1~1.5h, hydrolyze for 6.5~7h (from 100℃), cool and filter. Add 30% to 40% industrial sodium hydroxide solution to the filtrate under stirring. When the pH value reaches 3.0, add alkali solution at a slow speed until the pH value is 4.8. Leave it for 36 hours, separate the precipitate, and centrifuge to dryness to obtain bladder. Crude acid product (I), the mother liquor contains glutamic acid, arginine and leucine, etc. Weigh 150kg of crude cystine (I), add about 90kg of 10mol/L hydrochloric acid and 360kg of water, heat to 65~70°C, stir and dissolve for 0.5h, then add 12kg of activated carbon, heat to 80~90°C, and keep warm for 0.5h. Plate and frame filter press. Heat the filtrate to 80-85°C, add 30% sodium hydroxide while stirring, and stop when the pH reaches 4.8. Let it stand for the crystals to precipitate, siphon the supernatant, separate the bottom precipitate, and then centrifuge and spin dry to obtain crude cystine (II). Weigh 100kg of crude cystine (II), add 500L of 1mol/L hydrochloric acid, heat to 70°C, and then add 3 to 5kg of activated carbon. Then the temperature was raised to 85°C, kept stirred for 0.5h, and plate and frame filtered. Add distilled water about 1.5 times the volume of the filtrate to the filtrate, heat it to 75-80°C, and neutralize it with 12% ammonia water to pH 3.5-4.0 while stirring. At this time, cystine crystals will precipitate. The crystals are centrifuged to dryness, washed with distilled water until there is no chloride ion, and vacuum dried to obtain the finished product of cystine. The yield of human hair can reach 8%, and the yield of pig hair can reach 5%.

Purpose

1. Used for biochemical research. Preparation of biological culture media. It is used in biochemistry and nutrition research. In medicine, it can promote the oxidation and reduction functions of body cells, increase white blood cells and prevent the development of pathogenic bacteria. Mainly used for various types of alopecia. It is also used for acute infectious diseases such as dysentery, typhoid, and influenza, asthma, neuralgia, eczema, and various poisoning diseases, and has the effect of maintaining protein configuration. Also used as food flavoring.

2.Biochemical reagents, used for the preparation of biological culture media. It is also an important component of amino acid infusion and complex amino acid preparations.

3.Used as feed nutritional fortifier, it is beneficial to animal development, increases body weight and liver and kidney function, and improves fur quality.

4.Can be used as a cosmetic additive, which can promote wound healing, prevent skin allergies and treat eczema.

extended-reading:https://www.bdmaee.net/dabco-xd-104-dabco-tertiary-amine-catalyst-catalyst-xd-104/
extended-reading:https://www.bdmaee.net/dabco-t-96-catalyst-cas103-83-3-evonik-germany/
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/-NE1060-catalyst–NE1060-foam-catalyst–NE1060.pdf
extended-reading:https://www.cyclohexylamine.net/polyurethane-tertiary-amine-catalyst-catalyst-r-8020/
extended-reading:https://www.bdmaee.net/wp-content/uploads/2020/07/90-1.jpg
extended-reading:https://www.bdmaee.net/fascat2004-catalyst-cas7772-99-8-stannous-chloride/
extended-reading:https://www.newtopchem.com/archives/999
extended-reading:https://www.newtopchem.com/archives/40462
extended-reading:https://www.newtopchem.com/archives/39838
extended-reading:https://www.newtopchem.com/archives/39778

L-cystathionine

L-cystathionine structural formula

Structural formula

Business number 0182
Molecular formula C7H14N2O4S
Molecular weight 222.26
label

(R)-S-(2-amino-2-carboxyethyl)-L-cysteine,

(R)-S-(2-Amino-2-carboxyethyl)-L-homocysteine

Numbering system

CAS number:56-88-2

MDL number:MFCD00036685

EINECS number:200-295-8

RTECS number:None

BRN number:2505200

PubChem number:24892965

Physical property data

1. Character: Crystal.


2. Density (g/mL,25/4℃) : Undetermined


3. Relative vapor density (g/mL,AIR=1): Undetermined


4. Melting point (ºC): 240 250℃(262~263℃).


5. Boiling point (ºC,Normal pressure): Undetermined


6. Boiling point (ºC,5.2kPa): undetermined


7. Refractive index: not OK


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation ( º): Undetermined


10. Spontaneous ignition point or ignition Combustion temperature (ºC): not OK


11. Vapor Pressure (kPa,25ºC): Undetermined


12. Saturated vapor pressure (kPa,60ºC): Undetermined


13. Heat of combustion (KJ/mol): Undetermined


14. Critical temperature (ºC): Undetermined


15. Critical Pressure (KPa): Undetermined


16. Oil and water (octanol /Water) partition coefficient pair Value: Undetermined


17. Explosion limit (%,V/V): Undetermined


18. Lower explosion limit (%,V/V): not OK


19. Solubility: Not available Sure.

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

5. Molecular property data:


1. Molar refractive index: 52.59


2. Molar volume (m3/mol):155.4


3. Isotonic specific volume (90.2K):457.7


4. Surface Tension (dyne/cm):75.2


5. Polarizability10-24cm3): 20.84

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -6


2. Number of hydrogen bond donors: 4


3. Number of hydrogen bond acceptors: 6


4. Number of rotatable chemical bonds: 7


5. Number of tautomers:


6. Topological molecular polar surface area (TPSA):127


7. Number of heavy atoms: 14


8. Surface charge: 0


9. Complexity: 212


10. Number of isotope atoms: 0


11. Determine the number of atomic stereocenters: 2


12. The number of uncertain atomic stereocenters: 0


13. Determine the number of stereocenters of chemical bonds: 0


14. Uncertain number of chemical bond stereocenters: 0


15. Number of covalent bond units: 1

Properties and stability

None yet

Storage method

This product should be kept sealed.

Synthesis method

Generated by the interaction of o-succinyl homoserine and cysteine. Cystathionine is cystathionine betaLyase removes pyruvate and NH3generates homocysteine.

Purpose

For biochemical research.

extended-reading:https://www.newtopchem.com/archives/44415
extended-reading:https://www.morpholine.org/cas-616-47-7/
extended-reading:https://www.bdmaee.net/dabco-rp202-catalyst-cas31506-44-2-evonik-germany/
extended-reading:https://www.bdmaee.net/tributyltin-chloride-cas1461-22-9-tri-n-butyltin-chloride/
extended-reading:https://www.cyclohexylamine.net/foaming-catalyst-foaming-catalyst-blx-11/
extended-reading:https://www.newtopchem.com/archives/855
extended-reading:https://www.bdmaee.net/4-acetyl-morpholine/
extended-reading:https://www.newtopchem.com/archives/category/products/page/109
extended-reading:https://www.newtopchem.com/archives/44707
extended-reading:https://www.cyclohexylamine.net/tertiary-amine-catalyst-xd-103-catalyst-xd-103/

L-lysine

L-lysine structural formula

Structural formula

Business number 0181
Molecular formula C6H14N2O2
Molecular weight 146.19
label

(S)-2,6-diaminocaproic acid,

(S)-2,6-Diaminocaproic acid,

(S)-(+)-Lysine,

amino acid drugs,

intermediates,

Biochemical reagents

Numbering system

CAS number:56-87-1

MDL number:MFCD00064433

EINECS number:200-294-2

RTECS number:OL5540000

BRN number:1722531

PubChem number:24896404

Physical property data

1. Properties: Colorless needle-like crystals or crystalline powder. Optically active.

2. Density (g/mL, 25/4℃): 1.125

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): It turns black when heated to 210℃ and decomposes at 224.5℃.

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): α]D20 +14.6° (C=6.5, in water), [ α]D23+25.9° (C=2, in 6mol/L hydrochloric acid)

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure ( kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Oil-water (octanol/water) partition coefficient pair Value: Undetermined

17. Explosion upper limit (%, V/V): Undetermined

18. Explosion lower limit (%, V/V): Undetermined

19. Solubility: hygroscopic. Very soluble in water, slightly soluble in ethanol, almost insoluble in ether.

Toxicological data

1. Reproductive toxicity: Oral TDLo of female rats: 138mg/kg, conception takes 5-15 days; Oral TDLo of female rats: 72450mg/kg, conception takes 10-20 days; Oral TDLo of female rats: 90450mg/kg, Conception occurs after 10-20 days; oral TDLo for female rats: 81 mg/kg, conception occurs after 10-20 days; intraperitoneal TDLo for female rats: 44 mg/kg, conception occurs after 5-15 days 2. Mutagenicity: sister chromatid exchangeTEST system : Human lymphocytes: <SPAN lang=E BODY

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 38.43

2. Molar volume (cm3/mol): 129.9

3. Isotonic specific volume (90.2K ): 348.1

4. Surface tension (dyne/cm): 51.5

5. Polarizability (10-24cm3): 15.23

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 5

5. Number of tautomers: none

6. Topological molecule polar surface area 89.3

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 106

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 1

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Found in tobacco leaves.

Storage method

This product should be sealed and stored dry and below 0℃.

Synthesis method

1. L-lysine is generally supplied to the market as L-lysine hydrochloride [657-27-2]. Free L-lysine is easily deliquescent and prone to yellowing and deterioration due to its free amino groups. , and has a pungent fishy smell, making it difficult to store for a long time. L-lysine hydrochloride is relatively stable, not easy to deliquesce, and easy to store. However, the demand for L-lysine in some uses is also increasing, such as peptide synthesis chemistry, biochemical research, and preparation of lysine derivatives. Free L-lysine can be prepared from L-lysine hydrochloride.

2. Tobacco: BU, 22; FC, 21; can be obtained by hydrolysis and refining of animal protein. It can also be synthesized from benzoyl piperidine.

Purpose

For biochemical research. Medium preparation.

extended-reading:https://www.bdmaee.net/niax-a-100-composite-amine-catalyst-momentive/
extended-reading:https://www.newtopchem.com/archives/219
extended-reading:https://www.morpholine.org/category/morpholine/page/5395/
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/-DC5LE-reaction-type-delayed-catalyst-reaction-type-catalyst.pdf
extended-reading:https://www.bdmaee.net/bismuth-isooctanoate-cas67874-71-9-2-ethylhexanoic-acid-bismuth/
extended-reading:https://www.newtopchem.com/archives/category/products/page/165
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/Efficient-trimerization-catalyst-for-aliphatic-and-alicyclic-isocyanates.pdf
extended-reading:https://www.bdmaee.net/fascat4202-catalyst-dibutyltin-dilaurate-arkema-pmc/
extended-reading:https://www.bdmaee.net/kosmos-19-catalyst-cas121-73-6-degussa-ag/
extended-reading:https://www.newtopchem.com/archives/39593

Eugenol

eugenol structural formula

Structural formula

Business number 02CA
Molecular formula C10H12O2
Molecular weight 164.2
label

eugenol,

4-allyl-2-methoxyphenol,

1-Hydroxy-2-methoxy-4-allylbenzene,

4-allylguaiacol,

4-Allyl-2-methoxyphenol,

artificial flavors

Numbering system

CAS number:97-53-0

MDL number:MFCD00008654

EINECS number:202-589-1

RTECS number:SJ4375000

BRN number:1366759

PubChem number:24862128

Physical property data

1. Properties: Colorless or light yellow liquid, the color deepens when exposed to the air or under strong light. There is a strong clove aroma.

2. Melting point (ºC): -9.2~-9.1

3. Boiling point (ºC): 253.2

4. Relative density (20℃, 4 ℃): 1.0672

5. Relative density (25℃, 4℃): 1.065220

6. Refractive index at room temperature (n20 ): 1.5405

7. Refractive index at room temperature (n25): 1.534530

8. Dissolution Properties: Slightly soluble in water, soluble in ethanol, acetone, ethyl acetate, ether, chloroform and other organic solvents.

9.Flash point (℃): >110

Toxicological data

Toxicity classification Poisoning

Acute toxicity: Oral – Rat LD50: 1930 mg/kg; Oral – Mouse LC50: 3000 mg/kg.

Irritation Data: Skin – Rabbit 100 mg/24 hours Severe.

Ecological data

This substance is slightly hazardous to water.

Molecular structure data

1. Molar refractive index: 48.72

2. Molar volume (cm3/mol): 156.2

3. Isotonic specific volume (90.2K ): 384.3

4. Surface tension (dyne/cm): 36.5

5. Dielectric constant:

6. Dipole moment (10-24cm3):

7. Polarizability: 19.31

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: 3

6. Topological molecule polar surface area 29.5

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 145

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Avoid contact with oxides.

2. Colorless to light yellow liquid. Rich caramel sweet aroma. The color turns brown and black after being stored for a long time and exposed to air.

3. Exist in oriental tobacco leaves and smoke.

4. Found in clove oil, cinnamon leaf oil, cinnamon bark oil, camphor oil, nutmeg oil, etc.

Storage method

Brown glass bottle with light-sealed packaging. Store in a cool and dark place.

Synthesis method

1. Eugenol mainly exists in clove basil oil and camphor cinnamon leaf oil. It is a component of various aromatic oils, especially clove oil, cinnamon leaf oil, basil oil, and laurel oil. Although eugenol can also be prepared by synthetic methods, it is generally isolated and extracted from plants or aromatic oils in industry.

Take the clove basil and remove the fine roots and Foreign matter, dried and chopped, steam distilled. When distilling, maintain a strong fire and return the distillate to the pot to increase the oil yield. When the final steamed oil-water mixture is around 45°C, the relative density of the essential oil is close to water, and the distillate is white and turbid; when the temperature is between 30 and 40°C, part of the oil floats on the water (the relative density of ocimene is about 0.9) , the other part of the oil sinks underwater (the relative density of eugenol is greater than that of water).

Add 20% sodium hydroxide to the oil-water mixture, and then perform steam distillation to remove all non-acidic substances to obtain a eugenol sodium salt solution. Then add 30% sulfuric acid to neutralize it to pH=2~3 (water layer) with stirring at 50°C, let it stand and separate into layers, take off the crude eugenol oil in the lower layer and conduct distillation under reduced pressure to obtain eugenol.

It is produced by the reaction of o-methoxyphenol and allyl bromide, followed by heating and rearrangement.

2.Isolation method: Add excess sodium hydroxide aqueous solution to the natural essential oil containing eugenol, stir thoroughly, and This generates sodium eugenol that is soluble in water. After the oil layer is separated, the alkaline aqueous solution containing sodium eugenol is acidified with dilute sulfuric acid, and the eugenol is re-precipitated. Separate the eugenol oil layer, wash and dry it, and then distill it under reduced pressure to obtain refined eugenol.

3.The synthesis method uses o-methoxyphenol and allyl chloride as raw materials, in the presence of metallic copper, Heating to about 100℃, eugenol can be generated in one step. Since the boiling points of the three isomers are very close, the separation and purification work is very complicated. Therefore, the isolation method to generate eugenol is still the main method at present.

4. Tobacco: OR, 26; can be separated from clove oil. When the synthetic method uses guaiacol as raw material to prepare eugenol, there are many side reactions, and it is difficult to separate and purify.

Purpose

1. In addition to being used in medicine, it can also be used as a raw material for synthetic fragrances. It can also be used to prepare carnation-flavored daily flavors and can also be used as edible spices.

2.Mainly used for preparing mint, nuts, spicy foods and tobacco flavors. The dosage used in meat is 40~2000mg/kg; in gum, 500mg /kg; in condiments, 9.6~100mg/kg; in baked goods, 33mg/kg; 32 in candiesmg/kg; 3.1 in cold drinks mg/kg; 1.4mg/kg in soft drinks; 0.6 in puddings. In addition, eugenol has antiseptic and strong bactericidal properties and is found naturally in many essential oils.

3.Eugenol is the main fragrance agent for preparing clove, carnation, carnation and other flavors. It is used for preparing woody and oriental flavors. Fixatives and modifiers for fragrances. It is also often used in mint, nuts, spicy food flavors and tobacco flavors, and is also an important raw material for the synthesis of vanillin. It is also used in medicine and oral hygiene products. Eugenol is a commonly used analgesic drug in dentistry. It mainly anesthetizes dental nerves, slows down stimulation and plays an analgesic effect.

4. It is used in the blending of cosmetics, soaps, food and other flavors. Used in the ink industry as an anti-drying agent.

5. Also used as insecticide and preservative.

extended-reading:https://www.newtopchem.com/archives/45087
extended-reading:https://www.morpholine.org/nn-dicyclohexylmethylamine/
extended-reading:https://www.newtopchem.com/archives/39514
extended-reading:https://www.newtopchem.com/archives/862
extended-reading:https://www.newtopchem.com/archives/category/products/page/26
extended-reading:https://www.newtopchem.com/archives/1885
extended-reading:https://www.bdmaee.net/cas-3542-36-7/
extended-reading:https://www.morpholine.org/category/morpholine/
extended-reading:https://www.bdmaee.net/pentamethyldipropene-triamine-2/
extended-reading:https://www.newtopchem.com/archives/40413

rodentin

Raticide Structural Formula

Structural formula

Business number 01TJ
Molecular formula C14H14O3
Molecular weight 230.26
label

2-Pivaloyl-1,3-indandione,

The rat is over,

rodentin,

pintone,

2-(2,2-Dimethyl-1-oxopropyl)-1H-indene-1,3-(2H)dione,

Pival,

Pivalyl,

Pivacin,

,Pivaldion,

Pivalyn,

2-(2,2-Dimethyl-1-oxopropyl)-1H-indene-1,3-(2H)dione,

Rodenticide

Numbering system

CAS number:83-26-1

MDL number:MFCD00021230

EINECS number:201-462-8

RTECS number:NK6300000

BRN number:2051258

PubChem number:24899309

Physical property data

1. Character: bright yellow crystal

2. Density (g/mL, 25/4℃): Uncertain

3. &nb

Toxicological data

None

Ecological data

None

Molecular structure data

1. Molar refractive index: 61.75

2. Molar volume (cm3/mol): 192.3

3. Isotonic specific volume (90.2K ): 502.6

4. Surface tension (dyne/cm): 46.6

5. Polarizability (10-24cm3): 24.48

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.7

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 3

6. Topological molecule polar surface area 51.2

7. Number of heavy atoms: 17

8. Surface charge: 0

9. Complexity: 351

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

None

Synthesis method

None

Purpose

None

extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/stannous-octoate-CAS-301-10-0–T-9.pdf
extended-reading:https://www.bdmaee.net/catalyst-pt303-pt303-polyurethane-catalyst-pt303/
extended-reading:https://www.cyclohexylamine.net/cas-3164-85-0-k-15-k-15-catalyst/
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/-tmr-3-TMR-3-catalyst-?TMR.pdf
extended-reading:https://www.newtopchem.com/archives/43923
extended-reading:https://www.bdmaee.net/cas-683-18-1/
extended-reading:https://www.cyclohexylamine.net/category/product/page/25/
extended-reading:https://www.newtopchem.com/archives/44076
extended-reading:https://www.newtopchem.com/archives/44402
extended-reading:https://www.bdmaee.net/toyocat-dmi-gel-catalyst-tosoh/

BDMAEE:Bis (2-Dimethylaminoethyl) Ether

CAS NO:3033-62-3

China supplier

For more information, please contact the following email:

Email:sales@newtopchem.com

Email:service@newtopchem.com

Email:technical@newtopchem.com

BDMAEE Manufacture !