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Merck

33149

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
UNSPSC Code:
12352100
NACRES:
NA.21
PubChem Substance ID:
329754463
EC Number:
204-539-4
Beilstein/REAXYS Number:
508755
MDL number:
MFCD00003014

Key Documents

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Product Name

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

Quality Level

200

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

grade

ACS reagent
puriss. p.a.

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

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 DNA from various biological sources by colorimetric method. It may be used in the preparation of poly(diphenylamine), via electrochemical and chemical polymerization methods.

General description

Diphenylamine is an N-substituted derivative of aniline.

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

WGK 3

ppe

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class I Designated Chemical Substances

prtr

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

33149-250G-R: + 33149-6X100G-R: + 33149-6X250G-R: + 33149-INTR: + 33149-100G-R:4548173922201 + 33149-VAR-R: + 33149-BULK-R:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF4175
BCCB9503
BCBZ3928
BCBV1995
BCBR7243V

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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)
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
M Francklin Philips et al.
Journal of hazardous materials, 237-238, 46-54 (2012-09-12)
Poly(diphenylamine-co-2-aminobenzonitrile) (P(DPA-co-2ABN)), a cyano group containing conducting polyaniline derivative, has been electrodeposited developed as the new material and utilized for the simultaneous electrochemical determination of trace levels of cadmium (Cd(2+)) and lead (Pb(2+)). P(DPA-co-2ABN) film preconcentrates effectively through cyano chelation
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