2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol
2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol Basic information
- Product Name:
- 2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol
- Synonyms:
-
- 2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol
- N-methylamino-2-nitro-4-N',N'-bis(2-hydroxyethyl)aminobenzene
- HCBLUENO1
- HCBLUE1
- 1-Methylamino-2-nitro-4-(bis-2-hydroxyethyl) aminobenzene
- 2,2'-((4-(methylamino)-3-nitrophenyl)imino)bis-ethano
- 2,2'-((4-(methylamino)-3-nitrophenyl)imino)di-ethano
- 2,2'-((4-(methylamino)-3-nitrophenyl)imino)diethanol
- CAS:
- 2784-94-3
- MF:
- C11H17N3O4
- MW:
- 255.27
- EINECS:
- 220-495-9
- Mol File:
- 2784-94-3.mol
2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol Chemical Properties
- Melting point:
- 101.5-104 °C
- Boiling point:
- 398.5°C (rough estimate)
- Density
- 1.2235 (rough estimate)
- refractive index
- 1.5700 (estimate)
- pka
- 14.17±0.10(Predicted)
- IARC
- 2B (Vol. 57) 1993
- EPA Substance Registry System
- HC Blue 1 (2784-94-3)
Safety Information
- Hazardous Substances Data
- 2784-94-3(Hazardous Substances Data)
2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol Usage And Synthesis
Definition
ChEBI: HC Blue No.1 is a C-nitro compound.
General Description
Dark blue microcrystals or dark purple powder.
Air & Water Reactions
2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol may be sensitive to prolonged exposure to air. Slow oxidation. Insoluble in water.
Reactivity Profile
A nitrated aromatic, amine and alcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.
Fire Hazard
Flash point data for 2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol are not available; however 2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol is probably combustible.
2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol(2784-94-3)Related Product Information
- N-Phenyldiethanolamine
- 2-(4-Amino-3-nitroanilino)ethanol
- 4-Amino-3-nitro-N,N-dimethylaniline
- 3-DIETHYLAMINO-1-NITROBENZENE
- 2,2'-[[4-(methylamino)-3-nitrophenyl]imino]bisethanol
- N,N-DIMETHYL-3-NITROANILINE
- 2,2'-((4-((2-Hydroxyethyl)amino)-3-nitrophenyl)imino)bisethanol
- 1-[(2'-Methoxyethyl)amino]-2-nitro-4-[di-(2'-hydroxyethyl)amino]benzene
- 2,2'-(3-NITROPHENYLIMINO)-DIETHANOL
- 2-(2-Hydroxyethyl)-p-phenylenediamine