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2,5-diaminotoluene

2,5-Diaminotoluene
Diaminotoluene.png
Names
Preferred IUPAC name
2-Methylbenzene-1,4-diamine
Other names
2-Methyl-1,4-benzenediamine
Toluene-2,5-diamine
2,5-Diaminotoluene
Identifiers
ChEBI
ChemSpider
ECHA InfoCard 100.002.221
KEGG
UNII
Properties
C7H10N2
Molar mass 122.17
Appearance off white crystals
Density 1.107 g/cm3
Melting point 64 °C (147 °F; 337 K)
Boiling point 273 °C (523 °F; 546 K)
Hazards
Flash point no
US health exposure limits (NIOSH):
PEL (Permissible)
none
REL (Recommended)
Ca
IDLH (Immediate danger)
Ca [N.D.]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

2,5-Diaminotoluene is an organic compound with the formula C6H3(NH2)2CH3. It is one isomer of six with this formula. 2,5-Diaminotoluene is a colorless crystalline solid that is commonly used in hair coloring.

2,5-Diaminotoluene is prepared through electrolytic reduction of 2,5-dinitrotoluene. Other methods include the reductive cleavage of 4-amino-2,3'-dimethylazobenzene as well as the condensation of 2-amino-1-methylbenzene and toluene-4-sulphonyl chloride to produce 4-toluenesulphono-2-toluidide which is then coupled with diazotized aminobenzenesulphonic acid and reduced.

2,5-Diaminotoluene is a substitute for phenylenediamine (1,4-diaminobenzene) in commercial hair dyes. It is preferred because of its lower toxicity. However, many home hair dyes still use phenylenediamine. In these applications, these diamines function as a primary intermediate, which means that it is first oxidized with hydrogen peroxide and then combined with a coupler to form the hair dye. 2,5-Diaminotoluene is commonly used to produce black, drab and warm browns, and shades of blonde and gray hair dyes.

2,5-Diaminotoluene is also known to be used in the production of dyes for textiles, furs, leathers, biological stains and indicators, wood stains, and pigments. Two examples of dyes produced by 2,5-diaminotoluene are Cl Basic Red 2 and Cl Acid Brown 103.


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