추천 제품
vapor density
5.82 (vs air)
Quality Level
vapor pressure
1 mmHg ( 108 °C)
제품 라인
ReagentPlus®
분석
99%
autoignition temp.
1175 °F
bp
302 °C (lit.)
mp
50-53 °C (lit.)
solubility
water: insoluble
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
유전자 정보
human ... UGT1A4(54657)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Diphenylamine, a secondary aromatic amine, is an N-substituted derivative of aniline.
애플리케이션
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.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
표적 기관
Kidney,Liver,spleen
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Choose from one of the most recent versions:
이미 열람한 고객
"Determination of hair nicotine by gas chromatography?mass spectrometry"
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.
Nature, 206(4979) , 93-93 (1965)
Soluble and methane sulfonic acid doped poly (diphenylamine)-synthesis and characterization.
Materials Letters, 57(2), 280-290 (2002)
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
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
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