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4-Chloro-1,3-benzenediamine

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4-Chloro-1,3-benzenediamine Basic information

Product Name:
4-Chloro-1,3-benzenediamine
Synonyms:
  • 1,3-benzenediamine,-chloro-
  • 1-Chloro-2,4-Diaminobenzene
  • 4-Chloro-1,3-benzenediamine
  • 4-chloro-3-benzenediamine
  • 4-Chloro-meta-phenylenediamine
  • 4-chloro-m-phenylenediamin
  • 4-Chlorophene-1,3-diamine
  • 4-Chlorophenylene-1,3-diamine
CAS:
5131-60-2
MF:
C6H7ClN2
MW:
142.59
EINECS:
225-877-9
Mol File:
5131-60-2.mol
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4-Chloro-1,3-benzenediamine Chemical Properties

Melting point:
87-90 °C (lit.)
Boiling point:
232.49°C (rough estimate)
Density 
1.2124 (rough estimate)
refractive index 
1.5210 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
powder to crystal
pka
3.95±0.10(Predicted)
color 
White to Gray to Brown
Water Solubility 
<0.1 g/100 mL at 19 ºC
CAS DataBase Reference
5131-60-2(CAS DataBase Reference)
NIST Chemistry Reference
1,3-Benzenediamine, 4-chloro-(5131-60-2)
IARC
3 (Vol. 27, Sup 7) 1987
EPA Substance Registry System
4-Chloro-m-p.henylenediamine (5131-60-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 1673 6.1/PG 3
WGK Germany 
3
RTECS 
SS8800000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29215900
Hazardous Substances Data
5131-60-2(Hazardous Substances Data)

MSDS

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4-Chloro-1,3-benzenediamine Usage And Synthesis

Chemical Properties

Crystals. Soluble in ethanol; slightly soluble in water; insoluble in petroleum ether.

Uses

This compound has uses in dye production and in rubber processing.

Uses

4-Chloro-1,3-diaminobenzene has been used to study the mutagenic effect of phenylenediamines hair chemicals on Salmonella typhimurium TA 102.

Definition

ChEBI: 4-Chloro-meta-phenylenediamine is a member of monochlorobenzenes.

General Description

Gray powder or dark purple solid.

Air & Water Reactions

4-Chloro-1,3-benzenediamine is sensitive to prolonged exposure to light and air. Insoluble in water.

Reactivity Profile

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.

Health Hazard

ACUTE/CHRONIC HAZARDS: 4-Chloro-1,3-benzenediamine is a positive animal carcinogen and suspected human carcinogen.

Fire Hazard

Flash point data for 4-Chloro-1,3-benzenediamine are not available; however, 4-Chloro-1,3-benzenediamine is probably combustible.

Safety Profile

Suspected carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl and NOx. See also AROMATIC AMINES.

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