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Merck
CN

112763

Diphenylamine

99%, ReagentPlus®

Synonym(s):

N-Phenylbenzenamine, DBA, DFA, DPA

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About This Item

Linear Formula:
(C6H5)2NH
CAS Number:
122-39-4
Molecular Weight:
169.22
NACRES:
NA.21
PubChem Substance ID:
57646908
UNSPSC Code:
12352100
EC Number:
204-539-4
MDL number:
MFCD00003014
Beilstein/REAXYS Number:
508755

Key Documents

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Product Name

Diphenylamine, ReagentPlus®, 99%

InChI key

DMBHHRLKUKUOEG-UHFFFAOYSA-N

InChI

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

SMILES string

N(c1ccccc1)c2ccccc2

vapor density

5.82 (vs air)

vapor pressure

1 mmHg ( 108 °C)

product line

ReagentPlus®

assay

99%

autoignition temp.

1175 °F

bp

302 °C (lit.)

mp

50-53 °C (lit.)

solubility

water: insoluble

Quality Level

100

Gene Information

human ... UGT1A4(54657)

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Application

Diphenylamine may be used in the preparation of diphenylamine reagent, which is employed for the quantitative estimation of nucleic acid (DNA) from various biological sources by colorimetric method. It may be used in the preparation of poly(diphenylamine), via electrochemical and chemical polymerization methods. It can also be used as an internal standard in the determination of hair nicotine via gas chromatography coupled with mass spectrometry.

General description

Diphenylamine, a secondary aromatic amine, is an N-substituted derivative of aniline.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6618
SDBB4588
STBL4237
STBK9220
STBK5842

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"Determination of hair nicotine by gas chromatography?mass spectrometry"
Man NC, et al
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 877(03), 339-342 (2009)
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)
Margot Van der Jeught et al.
Stem cells and development, 22(2), 296-306 (2012-07-13)
In embryonic stem cell culture, small molecules can be used to alter key signaling pathways to promote self-renewal and inhibit differentiation. In mice, small-molecule inhibition of both the FGF/MEK/Erk and the GSK3β pathways during preimplantation development suppresses hypoblast formation, and
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