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D207756

Sigma-Aldrich

1,3-Diphenylguanidine

97%

Synonym(s):

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

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About This Item

Linear Formula:
(C6H5NH)2C=NH
CAS Number:
Molecular Weight:
211.26
Beilstein:
1875653
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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

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Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Occupational allergic contact dermatitis from diphenylguanidine in a gas mask.
M Bruze et al.
Contact dermatitis, 31(2), 125-126 (1994-08-01)
Mingxiang Lin et al.
Journal of pharmaceutical and biomedical analysis, 45(5), 747-755 (2007-10-12)
During the content uniformity test of a drug product (tablet formulation), an unknown peak was observed in the HPLC chromatograms. Upon further investigation, it was determined that the unknown peak was originated from an external source and, therefore, the drug
Allergy to rubber additives in orthopedic braces.
S T Bolhaar et al.
Contact dermatitis, 42(5), 288-289 (2000-05-02)
P V Shah et al.
Journal of toxicology and environmental health, 15(5), 623-633 (1985-01-01)
Dermal absorption, distribution, and metabolism of 1,3-diphenylguanidine (CAS 102-06-7) (DPG), widely used as an accelerator in processing rubber and in food packaging, was studied in adult female Sprague-Dawley rats. DPG shows 10% penetration through clipped back skin of the rats
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

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