InChI key
UBUCNCOMADRQHX-UHFFFAOYSA-N
InChI
1S/C12H10N2O/c15-13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
SMILES string
O=NN(c1ccccc1)c2ccccc2
grade
analytical standard
packaging
ampule of 1000 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
environmental
format
neat
storage temp.
room temp
Quality Level
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
target_organs
Bladder
signalword
Warning
Hazard Classifications
Aquatic Chronic 1 - Carc. 2 - Repr. 2 - Skin Sens. 1 - STOT RE 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
危险化学品
此项目有
Liquid chromatographic and thermal energy analyzer detection of N-nitrosodiphenylamine in formulations of diphenylamine.
Y Y Wigfield et al.
Bulletin of environmental contamination and toxicology, 45(6), 853-857 (1990-12-01)
James P Mattheis et al.
Journal of agricultural and food chemistry, 56(9), 3381-3385 (2008-04-03)
Diphenylamine metabolism and ethylene action were evaluated as factors influencing the development of 'Braeburn' apple internal browning and cavitation during cold storage. Apples treated with the antioxidant diphenylamine (DPA) and/or the ethylene action inhibitor 1-methylcyclopropene (1-MCP) were held at 1
Wen-Jun Zhou et al.
Environmental science & technology, 43(21), 8443-8448 (2009-11-21)
N-nitrosodiphenylamine (NDPhA) is a disinfection byproduct (DBP) in drinking water. However, it is not known what governs the formation of NDPhA and which precursor(s) in the raw water is responsible for its formation. We report here diphenylamine (DPhA) as a
Junghoon Choi et al.
Journal of environmental monitoring : JEM, 4(2), 249-252 (2002-05-08)
Studies were conducted to investigate the hypothesis that N-nitrosodimethylamine (NDMA) is a potential disinfection by-product specifically produced during chlorination or chloramination. Experiments were conducted using dimethylamine (DMA) as a model precursor. NDMA was formed by the reaction of DMA with
I C Felkner et al.
The Science of the total environment, 112(2-3), 177-188 (1992-03-01)
A new approach has been developed for assessing the toxicity and the metabolism of Group IV compounds and for other toxic substances that may interact with them at the molecular level. The approach is based upon the selective responses of
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