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33149

Sigma-Aldrich

Diphenylamine

puriss. p.a., suitable for redox indicator, ACS reagent, reag. Ph. Eur., ≥98% (GC)

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About This Item

Linear Formula:
(C6H5)2NH
CAS Number:
122-39-4
Molecular Weight:
169.22
Beilstein/REAXYS Number:
508755
EC Number:
204-539-4
MDL number:
MFCD00003014
UNSPSC Code:
12352100
PubChem Substance ID:
329754463
NACRES:
NA.21

$104.00

Available to ship onMay 20, 2025Details

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grade

ACS reagent
puriss. p.a.

Quality Level

200

agency

reag. Ph. Eur.

vapor density

5.82 (vs air)

vapor pressure

1 mmHg ( 108 °C)

assay

≥98% (GC)

autoignition temp.

1175 °F

technique(s)

titration: suitable

impurities

≤0.01% insoluble in ethanol

ign. residue

≤0.03% (as SO4)

bp

302 °C (lit.)

mp

50-53 °C (lit.)
52.5-54.0 °C

anion traces

nitrate (NO3-): in accordance

cation traces

Fe: ≤10 mg/kg

suitability

suitable for redox indicator

SMILES string

N(c1ccccc1)c2ccccc2

InChI

1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H

InChI key

DMBHHRLKUKUOEG-UHFFFAOYSA-N

Gene Information

human ... UGT1A4(54657)

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General description

Diphenylamine is an N-substituted derivative of aniline.[1]

Application

Diphenylamine may be used in the preparation of diphenylamine reagent, which is employed for the quantitative estimation of DNA from various biological sources by colorimetric method.[2][3] It may be used in the preparation of poly(diphenylamine), via electrochemical and chemical polymerization methods.[1]

Packaging

bottled under inert gas

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

target_organs

Kidney,Liver,spleen

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2631
BCCK2570
BCCH5691
BCCF4175
BCCB9503

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An improved diphenylamine method for the estimation of deoxyribonucleic acid.
Giles KW and Myers A.
Nature, 206(4979), 93-93 (1965)
A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid.
K BURTON
The Biochemical journal, 62(2), 315-323 (1956-02-01)
Soluble and methane sulfonic acid doped poly (diphenylamine)-synthesis and characterization.
Wen T-C, et al.
Materials Letters, 57(2), 280-290 (2002)
Walter J Jessen et al.
The Journal of clinical investigation, 123(1), 340-347 (2012-12-12)
Neurofibromatosis type 1 (NF1) patients develop benign neurofibromas and malignant peripheral nerve sheath tumors (MPNST). These incurable peripheral nerve tumors result from loss of NF1 tumor suppressor gene function, causing hyperactive Ras signaling. Activated Ras controls numerous downstream effectors, but
Sarah G Pati et al.
Environmental science & technology, 46(21), 11844-11853 (2012-09-29)
Dioxygenation of aromatic rings is frequently the initial step of biodegradation of organic subsurface pollutants. This process can be tracked by compound-specific isotope analysis to assess the extent of contaminant transformation, but the corresponding isotope effects, especially for dioxygenation of
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