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D207756

Sigma-Aldrich

1,3-Diphenylguanidine

97%

Sinónimos:

1,2-Diphenylguanidine, N,N′-Diphenylguanidine

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About This Item

Fórmula lineal:
(C6H5NH)2C=NH
Número de CAS:
102-06-7
Peso molecular:
211.26
Beilstein/REAXYS Number:
1875653
EC Number:
203-002-1
MDL number:
MFCD00001758
UNSPSC Code:
12352100
PubChem Substance ID:
24893619
NACRES:
NA.22

assay

97%

form

powder

mp

146-148 °C (lit.)

SMILES string

N=C(Nc1ccccc1)Nc2ccccc2

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

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

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

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

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Glove allergy due to 1,3-diphenylguanidine.
G Piskin et al.
Contact dermatitis, 54(1), 61-62 (2006-01-24)
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)
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
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%
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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