1,1′-(tetrathio two carbon sulfur) two piperidine 1,1 ‘- (4-thio two carbon sulfur) two piperidine

1,1'-(tetrathiobicarbonylthio)bipiperidine structural formula

Structural formula

Business number 03CE
Molecular formula C12H20N2S6
Molecular weight 384.69
label

Rubber accelerator DPTT,

Bispentamethylenethiuram tetrasulfide,

accelerator TRA,

Dipiperidinylthiuram-sulfide,

Disulfide carbonyl pentamethylene tetrasulfide,

Accelerator DPTT,

Four two-pentamethylene sulfide thiuram,

Promoter TRA,

2-piperidyl thiuram-sulfide,

Four disulfide carbonyl sulfide five azomethine,

accelerator,

Vulcanizing agent

Numbering system

CAS number:120-54-7

MDL number:MFCD00047474

EINECS number:204-406-0

RTECS number:TN4221000

BRN number:None

PubChem ID:None

Physical property data

1. Properties: White or grayish-yellow powder, odorless.
2. Melting point (℃): 115
3. Relative density (g/mL, 25/4℃): 1.50

Toxicological data

1. Acute toxicity: mouse abdominal LD50: 200mg/kg

Ecological data

None yet

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 106.85

2. Molar volume (cm3/mol): 267.5 

3. Isotonic specific volume (90.2K): 807.2

4. Surface tension (dyne/cm): 82.8

5. Dielectric constant: not determined.

6. Dipole moment (10-24cm3): Not yet determined.

7. Polarizability: 42.36

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 4.3

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 6

4. Number of rotatable chemical bonds: 5

5. Number of tautomers: none

6. Topological molecule polar surface area 172

7. Number of heavy atoms: 20

8. Surface charge: 0

9. Complexity: 294

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. Soluble in carbon disulfide, chloroform and carbon tetrachloride, but insoluble in water.
2. Non-toxic.

Storage method

Store in a cool, dry, ventilated place, away from direct sunlight. Valid for 1 year.

Synthesis method

Sodium pentamethylene dithiocarbamate is prepared from the reaction of hexahydropyridine, sodium carbonate and carbon disulfide, and then treated with sulfur monochloride to obtain bispentpentane tetrasulfide Methylenethiuram.

Purpose

This product is a thiuram vulcanization accelerator, which can be used in natural rubber, diene synthetic rubber, butyl rubber, EPDM rubber, chlorosulfonated polyethylene and latex. Heating can decompose free sulfur and can also be used as a vulcanizing agent. The effective sulfur content is 25% of its weight. When used as a vulcanizing agent, this product is relatively safe at the operating temperature. The vulcanized rubber has excellent heat resistance and aging resistance. This product is easily dispersed in dry rubber and water. Does not pollute. Generally used to manufacture heat-resistant products, cables, etc.

1,8-Dichloroanthraquinone 1,8-Dichloroanthraquinone

1,8-dichloroanthraquinone structural formula

1,8-dichloroanthraquinone structural formula

Structural formula

Business number 01SW
Molecular formula C14H6Cl2O2
Molecular weight 227.11
label

None

Numbering system

CAS number:82-43-9

MDL number:MFCD00001191

EINECS number:201-420-9

RTECS number:CB6496000

BRN number:None

PubChem number:24893952

Physical property data

1. Character: light yellow needle-like crystal


2. Density (g/mL,25/4℃): Unsure


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


4. Melting point (ºC): 202 203℃(199℃).


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


6. Boiling point (ºC,5.2kPa): Unsure


7. Refractive index: Uncertain


8. Flashpoint (ºC): Unsure


9. Specific optical rotation (º): Unsure


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


11. Vapor pressure (kPa,25ºC): Unsure


12.


2. Molar volume (m3/mol):182.9


3. isotonic specific volume (90.2K):509.1


4. Surface Tension (dyne/cm):59.9


5. Polarizability10-24cm3):27.13

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 4.1

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 34.1

7. Number of heavy atoms: 18

8. Surface charge: 0

9. Complexity: 350

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

Light yellow needle-shaped crystal. Soluble in nitrobenzene and hot toluene, slightly soluble in ethanol. It is yellow in concentrated sulfuric acid. Melting point202203℃ 199℃).

Storage method

Save sealed.

Synthesis method

None yet

Purpose

Manufacture of vat dyes, disperse dyes, organic pigments and pharmaceuticals.

t-family: Arial; mso-bidi-font-family: Arial; mso-font-kerning: 0pt”>~203℃199℃).

Storage method

Save sealed.

Synthesis method

None yet

Purpose

Manufacture of vat dyes, disperse dyes, organic pigments and pharmaceuticals.

1,1′-Iminodianthraquinone 1,1′-Iminodianthraquinone

1,1'-Iminodianthraquinone structural formula

1,1'-Iminodianthraquinone structural formula

Structural formula

Business number 01SS
Molecular formula C28H15NO4
Molecular weight 429.42
label

Di(1-anthraquinoyl)amine

Numbering system

CAS number:82-22-4

MDL number:MFCD00019132

EINECS number:201-405-7

RTECS number:CB7780000

BRN number:2607016

PubChem number:24860233

Physical property data

1. Character:Dark red needle-shaped crystalline powder


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


3. Relative vapor density ( g/mL,Air =1): No OK


4. Melting point (ºC):≥300


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


6. Boiling point (ºC,5.2kPa): Unsure


7. Refractive index: Uncertain


8. Flashpoint (ºC): Unsure


9. Specific optical rotation (º): Unsure


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


11. Vapor pressure (kPa,25ºC): Unsure


12. Saturated vapor pressure (kPa,60ºCExplosion limit (%,V/V): Unsure


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


19. Solubility:Soluble in concentrated sulfuric acid, it becomes a scarlet solution, and turns into olive green during storage. It is slightly soluble in aniline, nitrobenzene, chlorobenzene, and quinine. Phenoline is almost insoluble in organic solvents with low boiling points.


Toxicological data

2 , Neurotoxicity:


Rabbit skin test: 500 mg/24HREACTION; Rabbit eye test: 500 mg/24HREACTION;

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 120.45


2. Molar volume (m3/mol):294.7


3. isotonic specific volume (90.2K):864.6


4. Surface Tension (dyne/cm):74.0


5. Polarizability10-24cm3):47.75

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 5.9

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 5

6. Topological molecule polar surface area 80.3

7. Number of heavy atoms: 33

8. Surface charge: 0

9. Complexity: 783

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

Seal and store in a dark place.

Synthesis method

None yet

Purpose

For the determination of boron, germanium, selenium, tellurium and silicon.

ist 36.0pt” align=left>2. Molar volume (m3/mol):294.7


3. isotonic specific volume (90.2K):864.6


4. Surface Tension (dyne/cm):74.0


5. Polarizability10-24cm3):47.75

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 5.9

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 5

6. Topological molecule polar surface area 80.3

7. Number of heavy atoms: 33

8. Surface charge: 0

9. Complexity: 783

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

Seal and store in a dark place.

Synthesis method

None yet

Purpose

For the determination of boron, germanium, selenium, tellurium and silicon.

w-orphan; mso-margin-top-alt: auto; mso-margin-bottom-alt: auto” align=left>For the determination of boron, germanium, selenium, tellurium and silicon.

1,2-Dimethoxyethane 1,2-Dimethoxyethane

1,2-dimethoxyethane structural formula

Structural formula

Business number 031W
Molecular formula C4H10O2
Molecular weight 90.12
label

Ethylene glycol dimethyl ether,

1,2-Dimethoxyethane,

1,2-dimethoxyhexane,

1,2-Dimethylethane,

Ethylene glycol dimethyl ether,

1,2-Ethanediol dimethyl ether,

Dimethylglycol,

Ethylene glycol dimethyl ether,

Monoglyme,

paint stripper,

thinner,

Ether and acetal solvents

Numbering system

CAS number:110-71-4

MDL number:MFCD00008502

EINECS number:203-794-9

RTECS number:KI1451000

BRN number:1209237

PubChem number:24855712

Physical property data

1. Properties: colorless liquid with slight ether smell. [1]

2. Melting point (℃): -58[2]

3. Boiling point (℃): 82~83[3]

4. Relative density (water=1): 0.87 (20℃)[4]

5. Relative vapor density (air=1): 3.11[5]

6. Saturated vapor pressure (kPa): 6.40 (20℃)[6 ]

7. Heat of combustion (kJ/mol): -2521.2[7]

8. Critical temperature (℃): 263 [8]

9. Critical pressure (MPa): 3.87[9]

10. Octanol/water distribution Coefficient: -0.21[10]

11. Flash point (℃): -2 (CC)[11]

12. Ignition temperature (℃): 202[12]

13. Explosion upper limit (%): 18.7[13]

14. Lower explosion limit (%): 1.9[14]

15. Solubility: soluble in water, soluble in ethanol and hydrocarbons. [15]

16. Refractive index (n20ºC): 1.3796

17. Viscosity (mPa·s, 20ºC): 1.1

18. Heat of evaporation (KJ/mol): 28.14

19. Heat of fusion (KJ/kg): 139.4

20. Heat of formation (KJ/mol): 491.95

21. Heat of combustion (KJ/mol): 2520.82

22. Specific heat capacity (KJ/(kg·K), constant pressure): 1.83

23. Conductivity (S/m, 25ºC): 0.47×10-7

24. Vapor pressure (kPa, 20ºC): 6.40

25. Relative Density (20℃, 4℃): 0.8665

26. Relative density (25℃, 4℃): 0.855630

27. Critical density ( g·cm-3): 0.293

28. Critical volume (cm3·mol-1): 308

29. Critical compression factor: 0.269

30. Eccentricity factor: 0.346

31. Solubility parameter (J·cm-3

sup>)0.5: 17.732

32. van der Waals area (cm2·mol-1): 8.140 ×109

33. van der Waals volume (cm3·mol-1): 55.200

34. Gas phase standard combustion heat (enthalpy) (kJ·mol-1)���-2662.95

35. Gas phase standard claimed heat (enthalpy) (kJ·mol-1): -340.24

36. Liquid phase standard combustion Heat (enthalpy) (kJ·mol-1): -2626.65

37. The liquid phase standard claims heat (enthalpy) (kJ·mol-1): -376.64

38. Liquid phase standard hot melt (J·mol-1·K-1): 186.5

Toxicological data

1. Acute toxicity: Mouse oral LC50: 3200mg/kg; Rat oral LD50: >5000mg/kg; Rabbit oral LD50: 320mg/kg; Rat oral LDL0: 1000mg/kg; Rat Skin LD50: 5370mg/kg; rabbit skin LDL0: 2000mg/kg; rat inhalation LDL0: 63mg/m3/6H

2. It is of low toxicity by inhalation and oral administration. Inhaling high-concentration vapor can cause damage to the lungs, liver, kidneys and other organs.

3. Acute toxicity [16] LD50: 775mg/kg (rat oral)

Ecological data

This substance is slightly harmful to water bodies. Do not let this product come into contact with groundwater, waterways or sewage systems.

Molecular structure data

1. Molar refractive index: 24.07

2. Molar volume (cm3/mol): 1107.2

3. Isotonic specific volume (90.2K ): 230.6

4. Surface tension (dyne/cm): 21.3

5. Polarizability (10-24cm3): 9.54

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: 2

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 18.5

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 17.5

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. Chemical properties: stable in nature and difficult to react. But it can react with hydrogen iodide, hydrogen bromide and concentrated sulfuric acid. In the presence of acidic catalysts, decomposition can occur at high temperatures. Stable to alkali metals below 150°C, metallic sodium can be dried with ethylene glycol dialkyl ether. But it can react with sodium-potassium alloy or potassium. Phenyllithium and butyllithium slightly decompose ethylene glycol dimethyl ether. It does not react with low-activity Grignard reagents such as methylmagnesium chloride under normal conditions, but it decomposes when heated to 150~200°C with highly active reagents such as methylmagnesium iodide. It is stable to alkali metal hydrides and can be used as a stabilizer and refining agent for lithium aluminum hydride. Peroxide is generated under the action of oxygen, and light and heat promote the generation of peroxide. The generated peroxide is unstable and decomposes into aldehydes, ketones, acids and other impurities.

2. Stability[17] Stable

3. Incompatible substances[18] Strong oxidants, strong acids

4. Conditions to avoid contact [19] Air, light

5. Hazards of aggregation[20] No aggregation

Storage method

Storage Precautions[21] Usually products contain stabilizers. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37°C, and the packaging must be sealed and not in contact with air. They should be stored separately from oxidants and acids, and avoid mixed storage. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. Obtained from the reaction of ethylene glycol monomethyl ether and metal sodium; methyl chloride. Reflux ethylene glycol monomethyl ether and metal sodium together until the metal sodium reacts completely, cool the temperature to 45°C, and introduce methyl chloride. After the reaction is completed, perform fractional distillation and collect the 84-85.5°C fraction to obtain the finished product.

Refining method: The testing method for peroxide is the same as that for ether. The peroxides can be removed by refluxing with stannous chloride or by passing through activated alumina. Then add a small amount of metallic sodium to remove trace amounts of moisture. Other refining methods include drying with sodium wire and distilling with lithium aluminum hydride under nitrogen flow. You can also dry it with anhydrous calcium chloride for a few days, filter, add metallic sodium for distillation, or add lithium aluminum hydride to preserve it, and distill it before use.

2. Add metal sodium to ethylene glycol monomethyl ether in small amounts at 60°C while stirring. Control the temperature at 78-81°C. After adding metal sodium, cool down to 45°C. , and then pass in methyl chloride. The reaction formula is:

After the reaction is completed , distill, and collect the 84.5-85.5°C fraction to obtain ethylene glycol dimethyl ether.

3. After drying with sodium wire, add lithium aluminum hydride for distillation in the presence of nitrogen. You can also use anhydrous calcium chloride to dry for several days, filter out the calcium chloride, and then add metallic sodium for distillation, or Add lithium aluminum hydride and let it stand for distillation.

Purpose

1. Used as a solvent for nitrocellulose, resin, etc. and a solvent for preparing alkali metal oxides and borane. Aromatic hydrocarbons such as naphthalene, biphenyl, terphenyl, and anthracene form complexes with sodium in ethylene glycol dimethyl ether. Sodium-naphthalene complex is used for surface treatment when bonding fluorine-containing resins such as polytetrafluoroethylene. Sodium-biphenyl complex is used for the determination of halogens in gasoline. It can also be used to recover acetic acid from dilute acetic acid aqueous solution. It is also used as paint remover, thinner and to increase the viscosity of lubricating oil.

2. Used as solvents, pharmaceutical extraction agents, organic synthesis intermediates, catalysts, and corrosion inhibitors. [22]

Aromatic hydrocarbons form complexes with sodium in ethylene glycol dimethyl ether. Sodium-naphthalene complex is used for surface treatment when bonding fluorine-containing resins such as polytetrafluoroethylene. Sodium-biphenyl complex is used for the determination of halogens in gasoline. It can also be used to recover acetic acid from dilute acetic acid aqueous solution. It is also used as paint remover, thinner and to increase the viscosity of lubricating oil.

2. Used as solvents, pharmaceutical extraction agents, organic synthesis intermediates, catalysts, and corrosion inhibitors. [22]

1,4-Butanediol 1,4-Butanediol

1,4-butanediol structural formula

Structural formula

Business number 031N
Molecular formula C4H10O2
Molecular weight 90.12
label

butylene glycol,

1,4-Dihydroxybutane,

Butylene glycol,

1,4-Dihydroxybutane,

1,4-Butylene glycol,

Tetrasmethylene glycol,

softener,

water absorbent,

plasticizer,

lubricants,

humidifier,

softness,

adhesive,

Brightener for electroplating industry

Numbering system

CAS number:110-63-4

MDL number:MFCD00002968

EINECS number:203-786-5

RTECS number:EK0525000

BRN number:1633445

PubChem number:24854421

Physical property data

1. Properties: colorless viscous liquid, needle-like crystals at low temperatures.

2. Boiling point (ºC, 101.3kPa): 228

3. Melting point (ºC): 19.9

4. Relative density (g/mL, 20 /4ºC): 1.017

5. Relative density (g/mL, 25/4ºC): 1.015

6. Refractive index (n25ºC): 1.4445

7. Viscosity (mPa·s, 20ºC): 88.8

8. Viscosity (mPa·s, 25ºC): 45.27

9. Flash point (ºC, opening): >121

10. Heat of evaporation (KJ/kg): 576.1

11. Heat of combustion (KJ/mol): 2518.8

12. Specific heat capacity (KJ/( kg·K), 20~75ºC, constant pressure): 2.41

13. Critical temperature (ºC): 446

14 Critical pressure (MPa): 6.2

15 Thermal conductivity (W/(m·K), 20ºC): 0.160

16. Solubility: Miscible with water, acetone and alcohol. Slightly soluble in ether, benzene, halogenated hydrocarbons, etc.

17. Refractive index at room temperature (n20): 1.4462

18. Eccentricity factor: 1.189

19. Solubility parameter (J·cm-3)0.5:27.958

20. van der Waals area (cm2·mol-1): 8.320×109

21. van der Waals volume (cm3·mol– 1): 57.000

22. Gas phase standard combustion heat (enthalpy) (kJ·mol-1): -2576.5

23. Gas phase standard claims heat (enthalpy) (kJ·mol-1): -426.7

24. Liquid phase standardu-2% Bi/magnesium silicate (the number is the mass fraction of metal in the catalyst) is the catalyst, the reaction temperature is 95°C, the acetylene partial pressure is 0.1MPa, and the pH value is 5-6. An inert gas is used as a diluent to reduce the partial pressure of acetylene thereby minimizing the risk of explosion. The conversion rate of butyne dry cup alcohol based on formaldehyde is 95%, and propargyl alcohol is recovered. The theoretical yield of butynediol is 95%. The hydrogenation process was improved to two-stage hydrogenation: 35% butynediol aqueous solution and copper acetate flow into the continuous stirred tank reactor, using Ranny Ni as the catalyst, operating at a temperature of 50-60°C and a hydrogen pressure of 1.4-2.0MPa. Crude BDO vapor containing partially hydrogenated and carbonyl compounds is produced. The crude BDO vapor is hydrogenated again in a fixed bed reactor filled with Ni-Cu-Mn/silica gel catalyst. The reaction temperature is 120-140°C and the hydrogen pressure is 13.8-20.7MPa. ISP Company’s research found that the silica gel carrier degraded itself under the conditions of the second stage of high-pressure hydrogenation reaction, causing reactor pressure pulsation. To this end, a new catalyst composed of 15%Ni-7%Cu-05%Mn/AI was developed. The catalyst has high activity under reaction conditions, is self-stable, and has a long life. The yield of 1,4-butanediol was 93.1% based on acetylene.

2. Maleic anhydride hydrogenation method. The production processes using butane as raw material include: Huntsman/Kvaerner method, BPAmcoc/Lurgi Geminox method and Sisas method. Among them, the Kvaerner process is as follows: using a vanadium-based catalyst on a fixed bed to oxidize n-butane into maleic anhydride (MA) in the gas phase, then convert maleic anhydride into the corresponding dimethyl maleic anhydride (DMM), and further gas phase hydrogenation /Hydrolysis gives BDO. MA and excess methanol undergo esterification reaction to generate DMM. Using acidic ion exchange resin as catalyst, at 70-80℃, MA conversion rate is 100%, DMM The yield is 99%. The DMM gas phase hydrogenation process uses copper as the initiator. At 170-190°C and 4-7MPa, the hydrogen/ester feed molar ratio of the reaction system is usually (250-350):1. The yield of crude BDO and GHF obtained by hydrogenation is greater than 99% based on DMM feed. The crude product is continuously distilled through multiple towers and refined into BDO, γ-butyrolactone, and tetrahydrofuran products. The methanol is recovered and recycled to the chemical preparation process. The total BDO yield based on MA is 98%-99%, and the main by-product is butanol (0.1%-0.2%).

3. The butadiene method involves the acetyl oxidation reaction of 1,3- butadiene with acetic acid and oxygen to generate 1 , 4-diacetoxy-2-butene is produced by hydrogenation and hydrolysis. The by-products THF and acetic acid are recycled.

4,1,4-dichlorobutene method 1,4-dichloro Butene is an intermediate product in the process of producing chloroprene from butadiene. It is used as raw material and is hydrolyzed and hydrogenated to obtain 1,4-butanediol.

5. Preparation method:

With a stirrer , two reflux condensers, and a 3L reaction bottle with a dropping funnel, add 60g (2.6mol) of fresh metallic sodium, and quickly add 35g (0.2mol) of diethyl succinate (2) and 700mL of absolute ethanol. The reaction proceeds vigorously and can be cooled in an ice-water bath if necessary. After the reaction is stable, heat the reaction (bath temperature can reach 130°C) to complete the reaction of metallic sodium (about 0.5 to 1 hour). Cool in an ice-water bath and filter out the precipitated sodium chloride. Add 300g anhydrous potassium carbonate to the filtrate to remove water and acid. Filter, and the filter cake is extracted twice with hot ethanol. Combine the filtrate and extract, evaporate the ethanol, and solid salt will precipitate. Add dry acetone, filter, and evaporate the acetone. The residue was distilled under reduced pressure, and the fraction at 133-135°C/2.4kPa was collected to obtain 13g of 1,4-butanediol (1), with a yield of 72%. [1]

Purpose

1. 1,4-Butanediol has many uses. More than half of it is used in the production of tetrahydrofuran in the United States and Western Europe, followed by the production of γ-butyrolactone and polybutylene terephthalate, the latter of which is a rapidly developing engineering plastic; 1,4-butanediol is used as an Chain agents and polyester raw materials are used to produce polyurethane elastomers and flexible polyurethane foams; esters made from 1,4-butanediol are good additives for cellulose, polyvinyl chloride, polyacrylates and polyesters. Plasticizer. 1,4-Butanediol has good hygroscopicity and flexibility, and can be used as gelatin softener and water absorbent, as well as a treatment agent for cellophane and other unused paper. It can also be used to prepare N-methylpyrrolidone, N-vinylpyrrolidone and other pyrrolidone derivatives. It is also used to prepare vitamin B6, pesticides, herbicides and solvents, lubricants, humidifiers, softness, Intermediates for brighteners, solvents, wetting agents and plasticizers in the adhesive and electroplating industries. Cross-linking agent and organic synthesis for manufacturing polyurethane elastomers. It can prepare N-methylpyrrolidone, N-vinylpyrrolidone and other pyrrolidone derivatives, and is also used to prepare vitamin B6, pesticides and herbicides. 2.Basic organic chemical raw materials with high added value are widely used in the field of fine chemicals. It can produce tetrahydrofuran (TH-F), γ-butyrolactone (GBL), N-methylpyrrolidone and N-ethylpyrrolidone, and is also used to produce high-functional polybutyl terephthalate (PBT) and Important raw materials for polyester engineering plastics, elastic fibers, polyester polyol and polytetramethylene ether glycol (PTMEG), polyurethane artificial leather, thermoplastic rubber, adhesives and pharmaceuticals. It can also be used as a chain extender for polyurethane to produce unsaturated polyester resin, etc.

Intermediates for brighteners, solvents, wetting agents and plasticizers. Cross-linking agent and organic synthesis for manufacturing polyurethane elastomers. It can prepare N-methylpyrrolidone, N-vinylpyrrolidone and other pyrrolidone derivatives, and is also used to prepare vitamin B6, pesticides and herbicides. 2.Basic organic chemical raw materials with high added value are widely used in the field of fine chemicals. It can produce tetrahydrofuran (TH-F), γ-butyrolactone (GBL), N-methylpyrrolidone and N-ethylpyrrolidone, and is also used to produce high-functional polybutyl terephthalate (PBT) and Important raw materials for polyester engineering plastics, elastic fibers, polyester polyol and polytetramethylene ether glycol (PTMEG), polyurethane artificial leather, thermoplastic rubber, adhesives and pharmaceuticals. It can also be used as a chain extender for polyurethane to produce unsaturated polyester resin, etc.

1,4-Diaminobutane 1,4-Diaminobutane

1,4-diaminobutane structural formula

1,4-diaminobutane structural formula

Structural formula

Business number 031K
Molecular formula C4H12N2
Molecular weight 88.15
label

tetramethylenediamine,

1,4-Butanediamine,

1,4-Butylendiamine,

TetramethylenediaminePutrescine,

Putrecine,

linear compound

Numbering system

CAS number:110-60-1

MDL number:MFCD00008235

EINECS number:203-782-3

RTECS number:EJ6800000

BRN number:605282

PubChem number:24859702

Physical property data

1. Characteristics: colorless crystal with the smell of hexahydropyridine. [1]

2. Melting point (℃): 27~28[2]

3. Boiling point (℃) :158~160[3]

4. Relative density (water=1): 0.88[4]

5 .Octanol/water partition coefficient: -0.7[5]

6. Flash point (℃): 51.67[6]

7. Explosion upper limit (%): 9.1[7]

8. Explosion lower limit (%): 0.9[8]

9. Solubility: Easily soluble in water. [9]

Toxicological data

1. Acute toxicity[10] LD50: 463mg/kg (rat oral); 1576mg/kg (rabbit dermal)

2. Irritation No information

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3 .Non-biodegradability No information available

4. Other harmful effects[11] This substance is harmful to the environment and should be specially Pay attention to water pollution.

Molecular structure data

1. Molar refractive index: 27.65

2. Molar volume (cm3/mol): 101.9

3. Isotonic specific volume (90.2K ): 249.3

4. Surface tension (dyne/cm): 35.8

5. Polarizability (10-24cm3): 10.96

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -0.9

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 2

p>

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 52

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 17.5

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. Stability[12] Stable

2. Incompatible substances[13] Strong oxidants, acids, acid chlorides, acid anhydrides

3. Polymerization hazardsHarm[14] No aggregation

Storage method

Storage Precautions[15] Stored in a cool, ventilated warehouse. Keep away from fire and heat sources. The packaging is sealed. They should be stored separately from oxidants, acids, and food chemicals, and avoid mixed storage. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. Suitable materials should be available in the storage area to contain spills.

Synthesis method

1. Dioxime is obtained by reacting pyrrole with hydroxylamine hydrochloride, and then reduced to obtain butanediamine.

Purpose

1. Biochemical studies are used to stimulate the greening of chromatin. Organic Synthesis.

2. Used as chemical intermediates. [16]

1,8-Naphthalene dicarboxylic anhydride 1,8-Naphthalene dicarboxylic anhydride

1,8-naphthalenedicarboxylic anhydride structural formula

Structural formula

Business number 01SG
Molecular formula C12H6O3
Molecular weight 198
label

Naphthalene-1,8-dicarboxylic anhydride,

Naphtho[1,8,8a-c,d]pyran-1,3-dione,

Pesticide intermediates; aromatic carboxylic acids and their derivatives

Numbering system

CAS number:81-84-5

MDL number:MFCD00006925

EINECS number:201-380-2

RTECS number:QK5350000

BRN number:153190

PubChem number:24886009

Physical property data

1. Character: light yellow crystal

2. Density (g/mL, 25/4℃): Uncertain

3. Relative vapor density (g/mL, Air=1): Uncertain

4. Melting point (ºC): 274℃

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

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

7. Refractive index: Uncertain

8. Flash point (ºC): 272℃

9 . Specific rotation (º): Uncertain

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

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

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

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

14. Critical temperature (ºC): Uncertain

15. Critical pressure (KPa): Uncertain

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

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

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

19. Solubility : No boiling point, insoluble in water, ether, benzene, slightly soluble in hot ethanol, soluble in hot acetic acid.

Toxicological data

1. Acute toxicity

Rat caliber LD50: 12340 mg/kg; rat abdominal LD50: 200 mg/kg;

Mouse caliber LD50: 1600 mg/kg ;Mouse abdominal cavity LD50: 400 mg/kg;

Rabbit skin LD50:>2025mg/kg;

Bird caliber LD50: 4100 mg/kg;

Duck caliber LD50:>6180 mg/kg;

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 53.52

2. Molar volume (cm3/mol): 136.6

3. Isotonic specific volume (90.2K ): 388.0

4. Surface tension (dyne/cm): 64.9

5. Polarizability (10-24cm3):21.21

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: 3

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: None

6. Topological molecule polar surface area 43.4

7. Number of heavy atoms: 15

8. Surface charge: 0

9. Complexity: 282

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

This product is toxic. Its toxicity is similar to that of phthalic anhydride. It can irritate the eye mucosa and respiratory tract. Oral administration of LD5012340 mg/kg to rats. Contact with eyes and mouth should be avoided. Protective glasses and masks should be worn during operation. If accidentally contaminated, it can be treated as a general irritation.
 

Storage method

Keep sealed in a cool place. Packed in sacks lined with plastic bags to protect against heat, moisture and sun, and stored in a cool, ventilated and dry place. Store and transport according to regulations on toxic and hazardous
dangerous goods.

Synthesis method

Industrial acenaphthene is vaporized with primary air, mixed with secondary air, oxidized to 1,8-naphthalenedicarboxylic anhydride using cobalt as a catalyst, and then cooled.

Purpose

Used as an intermediate for dyes, pesticides, pharmaceuticals and polyester resins.

It is used to prepare fluorescent dyes and is also an important raw material for the synthesis of perylene dyes, pigments and fluorescent whitening agents, such as dispersed fluorescent yellow II and reduced gray BG.

1,4-Dichlorobutane 1,4-Dichlorobutane

1,4-dichlorobutane structural formula

1,4-dichlorobutane structural formula

Structural formula

Business number 031F
Molecular formula C4H8Cl2
Molecular weight 127.01
label

Tetramethylene dichloride,

tetramethylene chloride,

Tetramethylene dichloride,

1,4-Butylene dichloride,

Halogenated hydrocarbon solvents,

linear compound

Numbering system

CAS number:110-56-5

MDL number:MFCD00001011

EINECS number:203-778-1

RTECS number:None

BRN number:635673

PubChem number:24853989

Physical property data

1. Properties: colorless and transparent liquid with aromatic odor. [1]

2. Melting point (℃): -38[2]

3. Boiling point (℃): 161~163[3]

4. Relative density (water=1): 1.16[4]

5. Relative vapor density (air=1): 4.4[5]

6. Saturated vapor pressure (kPa): 0.53 (20℃)[6]

7. Critical pressure (MPa): 3.61[7]

8. Octanol/water partition coefficient: 2.81[8]

9. Flash point (℃): 40[9]

10. Ignition temperature (℃): 220 [10]

11. Explosion upper limit (%): 8.9[11]

12. Explosion lower limit (%): 1.8[12]

13. Solubility: Insoluble in water, soluble in most organic solvents. [13]

14. Refractive index at room temperature (n25): 1.4522

15. Relative density (25℃, 4℃): 1.1353

16. Solubility parameter (J·cm-3)0.5: 19.570

17. van der Waals area (cm2·mol-1): 9.000×109

18. van der Waals Volume (cm3·mol-1): 64.160

Toxicological data

1. Acute toxicity No data available

2. Irritation No data available

Ecological data

1. Ecotoxicity No information available

2. Biodegradability No information available

3 .Non-biodegradability No information available

Molecular structure data

1. Molar refractive index: 30.27

2. Molar volume (cm3/mol): 117.3

3. Isotonic specific volume (90.2K ): 268.1

4. Surface tension (dyne/cm): 27.2

5. Polarizability (10-24cm3): 12.00

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: 0

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 0

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 17.5

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12.The number of uncertain stereocenters of atoms: 0

13. The number of determined stereocenters of chemical bonds: 0

14. The number of uncertain stereocenters of chemical bonds: 0

15. Number of covalent bond units: 1

Properties and stability

1. It is flammable. It is flammable when exposed to open flames or high heat. It can release highly toxic phosgene when decomposed by heat.

2. Stability[14] Stable

3. Incompatible substances[15] Strong oxidizing agent, strong alkali

4. Conditions to avoid contact[16] Heating

5. Polymerization hazard[17] No polymerization

6. Decomposition products[18] Hydrogen chloride, phosgene

Storage method

Storage Precautions[19] Stored in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37°C. Keep container tightly sealed. They should be stored separately from oxidants and alkalis, and avoid mixed storage. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. Obtained from the reaction of chlorobutane and chlorine.

2. Obtained from the reaction of tetrahydrofuran and hydrochloric acid.

Purpose

1. Used as raw materials and solvents for organic synthesis. Used in the synthesis of adiponitrile, the drug Kebiqing, etc.

2. Used as an intermediate in organic synthesis. [20]

1,4-Dibromobutane 1,4-Dibromobutane

1,4-dibromobutane structural formula

Structural formula

Business number 031C
Molecular formula C4H8Br2
Molecular weight 215.93
label

Butylene dibromide,

Tetramethyl bromide,

propylene bromide,

Tetramethylenyl dibromide,

Tetramethylene dibromide,

tetramethylene bromide,

Butylene dibromide,

1,4-Butylene bromide,

Tetramethylene dibromide,

linear compound

Numbering system

CAS number:110-52-1

MDL number:MFCD00000261

EINECS number:203-775-5

RTECS number:EJ7565000

BRN number:1071199

PubChem number:24848480

Physical property data

1. Properties: colorless or light yellow liquid.

2. Density (g/mL, 25℃): 1.808

3. Relative density (20℃, 4℃): 1.8265

4. Melting point (ºC): -20

5. Boiling point (ºC, normal pressure): 197.5

6. Relative density (25℃, 4℃): 1.8187

7. Refractive index at room temperature (n20): 1.5190

8. Flash point (ºC): >110

9. Refractive index at room temperature (n 25): 1.5169

10. The gas phase standard claims heat (enthalpy) (kJ·mol-1): -87.0

11. Liquid phase standard claims heat (enthalpy) (kJ·mol-1): -140.1

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

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

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined Determined

16. Logarithmic 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 chloroform, alcohol and ether, insoluble in water.

Toxicological data

None yet

Ecological data

This substance is not harmful to water bodies.

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 36.04

2. Molar volume (cm3/mol): 120.9

3. Isotonic specific volume (90.2K): 295.5

4. Surface tension (dyne/cm): 35.6

5. Polarizability (10-24cm3): 14.28

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.5

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 0

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 0

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 17.5

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. Stable in nature, it will not decompose under normal temperature and pressure. Avoid contact with oxides.

2. It is locally irritating and has an anesthetic effect at high concentrations.

Storage method

1. Store in a cool, ventilated warehouse, away from fire. Keep container tightly sealed and store away from oxidizing agents. Emergency release equipment and suitable containment materials should be available.

2. Packed in 250kg iron drum.

Synthesis method

1, obtained from tetrahydrofuran through ring opening and bromination. Add hydrobromic acid to the reaction pot, add tetrahydrofuran dropwise while stirring, and then add sulfuric acid dropwise. The temperature is controlled at 50℃below. Then heat up to108℃Reflux around4h, continue stirring after the reaction is completed 1h, let cool to separate the supernatant, wash with soda ash solution until neutral, add anhydrous calcium chloride to dry, filter to obtain the finished product.

2, by1,4- Butanediol is obtained by bromination. Add hydrobromic acid into the reaction pot, stir and cool until 10℃, add sulfuric acid dropwise. After the addition is completed, add 1,4- butanediol dropwise, and the temperature should not exceed 15℃, stir for half an hour. in100-110℃ insulation 6h. Cool to room temperature, separate the supernatant, and wash with soda ash solution until neutral. After dehydration of calcium chloride, 1,4-dibromobutane is obtained by filtration.

3. Preparation method: span>

In a reaction bottle equipped with a stirrer, reflux condenser, and dropping funnel, add 154g (105mL) of 48% hydrobromic acid. Cool in an ice-water bath, and slowly add 70 mL of concentrated sulfuric acid while stirring. Add 30g (0.33mol) of newly distilled 1,4-butanediol (2) dropwise, and leave it at room temperature for 24 hours after the addition. The reaction was heated in a boiling water bath for 3 hours. The reaction mixture was divided into two layers, and the lower layer was separated, washed with water, 5% sodium carbonate, and water in sequence, and dried over anhydrous magnesium sulfate. Distill under reduced pressure and collect the distillate of Kuli at 83~84℃/1.6kPa to obtain 55g of 1,4-dibromobutane (1) with a yield of 76%. [1]

Purpose

Organic synthesis intermediates, used in the manufacture of aminophylline, Kebiqing, Ququjing, etc. Used in the manufacture of aminophylline, Kebiqing, Qiqujing, etc.

1,8-Naphthalimide 1,8-Naphthalimide

1,8-naphthalenedicarboximide structural formula

1,8-naphthalenedicarboximide structural formula

Structural formula

Business number 01SF
Molecular formula C12H7NO2
Molecular weight 197.19
label

None yet

Numbering system

CAS number:81-83-4

MDL number:MFCD00006920

EINECS number:201-379-7

RTECS number:None

BRN number:153150

PubChem number:24897515

Physical property data

1. Appearance: Off-white to white powder 2. Density (g/mL, 25/4℃): Uncertain

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

4. Melting point (ºC): 299

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

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

p>

7. Refractive index: Uncertain

8. Flash point (ºC): Uncertain

9. Specific rotation (º): Uncertain

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

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

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

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

14. Critical temperature (ºC): Uncertain

15. Critical pressure (KPa): Uncertain

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

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

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

19. Solubility: Uncertain

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 55.26

2. Molar volume (cm3/mol): 141.6

3. Isotonic specific volume (90.2K ): 395.9

4. Surface tension (dyne/cm): 61.0

5. Polarizability (10-24cm3): 21.90

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: 0

5. Number of tautomers: 2

6. Topological molecule polar surface area 46.2

7. Number of heavy atoms: 15

8. Surface charge: 0

9. Complexity: 285

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 sealed and stored in a dry and dark place.

Synthesis method

Obtained from the amination of 1,8-naphthalenedicarboxylic acid. Add 290kg of 1,8-naphthalenedicarboxylic acid; 414kg of 20% ammonia water and 414kg of water into the reaction pot, heat to 100-110°C, and the pressure is 0.2-0.25MPa. Keep warm for 5 hours. Then cool to below 40°C, filter and wash to obtain 242kg of 1,8-naphthalenedicarboximide.

Purpose

Dye intermediates. Used to synthesize perylene dyes and pigments, such as reduced gray BG, reduced brilliant orange 3RK, soluble anthracene brilliant orange IRK and fluorescent whitening agents, etc. Also used in the preparation of pesticides.

BDMAEE:Bis (2-Dimethylaminoethyl) Ether

CAS NO:3033-62-3

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