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线性分子式:
(C6H5NH)2C=NH
化学文摘社编号:
分子量:
211.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-002-1
Beilstein/REAXYS Number:
1875653
MDL number:
Assay:
97%
Form:
powder
InChI
1S/C13H13N3/c14-13(15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H,(H3,14,15,16)
InChI key
OWRCNXZUPFZXOS-UHFFFAOYSA-N
SMILES string
N=C(Nc1ccccc1)Nc2ccccc2
assay
97%
form
powder
Quality Level
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
rat ... Grin2a(24409), Scnn1g(24768)
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
338.0 °F - closed cup
flash_point_c
170 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
J M Schaeffer et al.
Biochemical pharmacology, 48(2), 411-418 (1994-07-19)
A series of dibenzo[a,d]cycloalkenimines were evaluated for their affinity to the (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (MK-801) binding site in Caenorhabditis elegans membranes and their nematocidal activity. The (+)-MK-801 enantiomer (1) had a higher affinity (Kd = 240 nM) for its specific binding site
Lymphomatoid allergic contact dermatitis mimicking cutaneous T cell lymphoma.
Meghan T Hession et al.
Dermatitis : contact, atopic, occupational, drug, 21(4), 220-220 (2010-07-22)
M A Bempong et al.
Journal of toxicology and environmental health, 11(4-6), 869-878 (1983-04-01)
The effects of 1,3-diphenylguanidine (DPG) on seminal cytology in hybrid mice and inbred Syrian golden hamsters and on testicular histology and reproductive toxicity in mice were monitored. Treatment consisted of chronic exposure of hamsters and mice to DPG in 0.025%
Glove allergy due to 1,3-diphenylguanidine.
G Piskin et al.
Contact dermatitis, 54(1), 61-62 (2006-01-24)
B Clement et al.
Xenobiotica; the fate of foreign compounds in biological systems, 23(2), 155-167 (1993-02-01)
1. The enzymic C-oxygenation of N,N'-diphenylguanidine (DPG) to N-(4-hydroxyphenyl)-N'-phenylguanidine (4HPG) and the N-oxygenation of N,N'-bis-(pentafluorophenyl)-guanidine (BPG) to N"-hydroxy-N,N"-bis-(pentafluorophenyl)-guanidine (HBPG) is reported. 2. The metabolites were identified by t.l.c. and mass spectral analysis using synthetic reference compounds. 3. Rat and rabbit
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