solid blue BB

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solid blue BB structural formula

Structural formula

Business number 03BL
Molecular formula C17H20N2O3
Molecular weight 300.36
label

Solid Blue BB,

N-(4-amino-2,5-diethoxyphenyl)benzamide,

4′-Amino-2′,5′-diethoxybenzanilide,

Azoic Diazo No. 20,

Fast blue BB,

Reagent

Numbering system

CAS number:120-00-3

MDL number:MFCD00009091

EINECS number:204-363-8

RTECS number:None

BRN number:3416889

PubChem number:24894715

Physical property data

1. Characteristics: Light gray or off-white powder.


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


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


4. Melting point (ºC): 98- 100


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


6. Boiling point (ºC, KPa): 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 (mmHg,ºC): Undetermined


12. Saturated vapor pressure (kPa, ºC): 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 for water: undetermined


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


3 Isotonic specific volume (90.2K): 665.6


4, Surface Tension (dyne/cm):548.9


5 Polarizability (10-24cm3):34.76

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.8

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 6

5. Number of tautomers: 2

6. Topological molecule polar surface area 73.6

7. Number of heavy atoms: 22

8. Surface charge: 0

9. Complexity: 345

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

Use hydroquinone as raw material, alkylate with ethyl chloride, then nitrate with nitric acid, reduce with sodium sulfide, and then use benzene Formyl chloride is acylated, then nitrated with nitric acid, reduced by pyridine and sodium bisulfite, and refined, filtered and dried. Raw material consumption (kg/t) Hydroquinone (98%) 560 Nitric acid (98%) 930Ethyl chloride (95% ) 930 Hydrochloric acid 710 Benzoyl chloride (98%) 630 Sodium sulfide (63.5%) 1040Pyridine (98%) 32 Sodium bisulfite (95%) 1030Caustic soda (100%) 970 Ammonium chloride (98%) 70 Pure carbon (98%) 700 Zinc ingot 110

Purpose

Mainly used as a developer for dyeing and printing cotton, viscose and silk fabrics, and is more suitable for resist dyeing printing. It is less used for dyeing alone and is not easy to remove the dye.

2>

Use hydroquinone as raw material, alkylate with ethyl chloride, then nitrate with nitric acid, reduce with sodium sulfide, and then use benzene Formyl chloride is acylated, then nitrated with nitric acid, reduced by pyridine and sodium bisulfite, and refined, filtered and dried. Raw material consumption (kg/t) Hydroquinone (98%) 560 Nitric acid (98%) 930Ethyl chloride (95% ) 930 Hydrochloric acid 710 Benzoyl chloride (98%) 630 Sodium sulfide (63.5%) 1040Pyridine (98%) 32 Sodium bisulfite (95%) 1030Caustic soda (100%) 970 Ammonium chloride (98%) 70 Pure carbon (98%) 700 Zinc ingot 110

Purpose

Mainly used as a developer for dyeing and printing cotton, viscose and silk fabrics, and is more suitable for resist dyeing printing. It is less used for dyeing alone and is not easy to remove the dye.

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