1,5-Diaminoanthraquinone 1,5-Diaminoanthraquinone

1,5-diaminanthraquinone structural formula

1,5-diaminanthraquinone structural formula

Structural formula

Business number 03LZ
Molecular formula C14H10N2O2
Molecular weight 238.25

1,5-diamine enquinsulfonic acid,


aromatic compounds

Numbering system

CAS number:129-44-2

MDL number:MFCD00001226

EINECS number:204-947-2

RTECS number:CB6400000

BRN number:None

PubChem number:24862850

Physical property data

1. Properties: dark red needle crystals (in ethanol, acetic acid).

2. Melting point (decomposition, ℃): 308

3. Solubility: soluble in hot nitrobenzene, slightly soluble in ethanol, ether, benzene, acetone, and chloroform. The solution in concentrated sulfuric acid is almost colorless.

Toxicological data

1. Skin/eye irritation: Rabbit eye standard Drez eye dye test: 500mg/24H has a slight irritating effect on the eyes.

2. Acute toxicity: rat transperitoneal LD5O: 1300mg/kg

3. Mutagenicity: Salmonella gene mutation testing system: 500ug/plate

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 67.14

2. Molar volume (cm3/mol): 163.6

3. Isotonic specific volume (90.2K ): 490.7

4. Surface tension (dyne/cm): 80.9

5. Polarizability (10-24cm3): 26.61

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.6

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 15

6. Topological molecule polar surface area 86.2

7. Number of heavy atoms: 18

8. Surface charge: 0

9. Complexity: 346

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

Basic properties

Red-brown needle-like crystals. Melting point 319℃. Soluble in hot nitrobenzene, slightly soluble in ethanol, ether, benzene, chloroform and acetone, insoluble in water. Heating and sublimation.

Storage method

None yet

Synthesis method

The nitrification reduction method is mainly used. Anthraquinone is used as raw material. It is nitrated with mixed acid in concentrated sulfuric acid to obtain 1,5-dinitroanthraquinone and 1,8-diaminanthraquinone. After filtering and washing, they are then reduced with sodium sulfide, and then Obtained by filtering, washing and drying.


Dye intermediates. Mainly used to prepare anthraquinone reduction dyes reduction yellow 3RT, reduction orange 3G, reduction orange 3C, reduction gray 3Y, and other anthraquinone dyes such as��Lan et al.

BDMAEE:Bis (2-Dimethylaminoethyl) Ether

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