2,4-Disulfonic acid aniline

2,4-Disulfonic acid aniline structural formula

2,4-Disulfonic acid aniline structural formula

Structural formula

Business number 03RN
Molecular formula C6H7NO6S2
Molecular weight 253.25
label

4-amino-1,3-benzenedisulfonic acid,

Aniline-2,4-disulfonic acid,

4-Amino-1,3-benzenedisulfonic acid,

Heterocyclic compounds

Numbering system

CAS number:137-51-9

MDL number:None

EINECS number:205-299-3

RTECS number:None

BRN number:None

PubChem ID:None

Physical property data

None

Toxicological data

None

Ecological data

None

Molecular structure data


Molecular property data:


1, Molar refractive index51.06


2, Molar volumem3/mol):137.2


3 isotonic ratio90.2K):423.1


4 Surface tension(3.0 dyne/cm) :90.2


5 Polarizability0.5 10-24cm3):20.24

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: 7

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: none

6. Topological molecule polar surface area 152

7. Number of heavy atoms: 15

8. Surface charge: 0

9. Complexity: 416

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

It is obtained by sulfonation of p-aminobenzene sulfonic acid through fuming sulfuric acid. Put 20% into the sulfonation pot20%Oleum, with stirring Slowly add dry p-aminobenzene sulfonic acid, and control the temperature during addition50, add ingredients and stir20min, then warm to 60, insulation1h, and then up to80Insulation1h, and then raised to 100 , insulation 1h, and finally upgraded to 128, insulating5h, sampling and verification (take samples10 -24cm3):20.24

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: 7

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: none

6. Topological molecule polar surface area 152

7. Number of heavy atoms: 15

8. Surface charge: 0

9. Complexity: 416

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

It is obtained by sulfonation of p-aminobenzene sulfonic acid through fuming sulfuric acid. Put 20% into the sulfonation pot20%Oleum, with stirring Slowly add dry p-aminobenzene sulfonic acid, and control the temperature during addition50, add ingredients and stir20min, then warm to 60, insulation1h, and then up to80Insulation1h, and then raised to 100 , insulation 1h, and finally upgraded to 128, insulating5h, sampling and verification (take samples2ml, diluted in40mlIn distilled water, shake to make it whole Dissolve, subject to obtaining a clear solution). Again128Stir3h, then cool to 75Discharge, yield98%

Purpose

Can be used as dye intermediate

N lang=EN-US style=”COLOR: #333333; FONT-FAMILY: Times New Roman; mso-bidi-font-size: 10.5pt”>2ml, diluted in40mlDistilled water, shake to completely dissolve, subject to a clear solution). Again128Stir3h, then cool to 75Discharge, yield98%

Purpose

Can be used as dye intermediate

BDMAEE:Bis (2-Dimethylaminoethyl) Ether

CAS NO:3033-62-3

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