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N21200

Sigma-Aldrich

2-Nitro-1,4-phenylenediamine

95%

Synonym(s):

1,4-Diamino-2-nitrobenzene, 2-Nitro-p-phenylenediamine

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100 G
$68.32

$68.32

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100 G
$68.32

About This Item

Linear Formula:
O2NC6H3(NH2)2
CAS Number:
5307-14-2
Molecular Weight:
153.14
Beilstein/REAXYS Number:
2210195
EC Number:
226-164-5
MDL number:
MFCD00007903
UNSPSC Code:
12352100
PubChem Substance ID:
24897551
NACRES:
NA.22

$68.32

List Price$97.60Save 30%
Web-Only Promotion

Available to ship onApril 29, 2025Details

Request a Bulk Order

Quality Level

100

assay

95%

form

powder

mp

135-138 °C (lit.)

SMILES string

Nc1ccc(N)c(c1)[N+]([O-])=O

InChI

1S/C6H7N3O2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H,7-8H2

InChI key

HVHNMNGARPCGGD-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

Hazard Classifications

Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

>372.2 °F - Pensky-Martens closed cup

flash_point_c

> 189 °C - Pensky-Martens closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8291
STBG4487V
STBD4690V
S19927
04716KE

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Sigma-Aldrich

305065

1,2,4,5-Benzenetetramine tetrahydrochloride

Metabolism of the hair dye component, nitro-p-phenylenediamine, in the rat.
M Nakao et al.
Chemical & pharmaceutical bulletin, 35(2), 785-791 (1987-02-01)
1,4-Diamino-2-nitrobenzene (2-nitro-para-phenylenediamine).
IARC monographs on the evaluation of carcinogenic risks to humans, 57, 185-200 (1993-01-01)
S Bala et al.
Mutation research, 222(3), 141-148 (1989-03-01)
The antimutagenic effect of 10 citrus fruit juices was observed against the mutagenicity of N-nitro-o-phenylenediamine (NPD) in TA97a and sodium azide in TA100 tester strains of Salmonella typhimurium using the Ames test. It was noticed that the juices of all
M Nakao et al.
Chemical & pharmaceutical bulletin, 38(9), 2561-2566 (1990-09-01)
Regioselectivity in N-acetylation of nitro-0-phenylenediamine, a widely used hair dye component, by rat liver cytosolic N-acetyltransferases was studied in relation to its substituent effects on enzymatic N-acetylation of mono-substituted anilines. Nitro-p-phenylenediamine was acetylated specifically at the N4-position to afford the
In vivo skin penetration studies of 2,4-toluenediamine, 2,4-diaminoanisole, 2-nitro-p-phenylenediamine, p-dioxane and N-nitrosodiethanolamine in cosmetics.
F N Marzulli et al.
Food and cosmetics toxicology, 19(6), 743-747 (1981-12-01)
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