| Weight | 268.36 g/mol |
|---|---|
| Formula | C17H20N2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Centralite (85-98-3)
diethyldiphenylurea · N,N'-diethylcarbanilide
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- Desorption electrospray tandem MS (DESI-MSMS) analysis of methyl centralite and ethyl centralite as gunshot residues on skin and other surfaces. (Journal of Forensic Sciences, 2008)
- Chromatographic Investigations of Smokeless Powder. Derivatives of Centralite Formed in Double-Base Powders During Accelerated Aging. (Industrial & Engineering Chemistry, 1950)
- Detection of N,N-diphenyl-N,N-dimethylurea (methyl centralite) in gunshot residues using MS-MS method (Analyst, 1999)
- Centralit des marges et dynamique des centres (1986)
- Fluorescence Detection of Ethyl Centralite in Gunshot Residues (Journal of Forensic Sciences, 1994)
- Voltammetric determination of the stabilizing additives acardite II, centralite I and diphenylamine in propellants. (Talanta, 1985)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - diethyldiphenylurea
- N,N'-diethylcarbanilide
-
SMILESCCN(C1=CC=CC=C1)C(=O)N(CC)C2=CC=CC=C2
-
InChIKeyPZIMIYVOZBTARW-UHFFFAOYSA-N
- Pubchem - Centralite
- Wikipedia - N,N'-diethylcarbanilide
Centralite (empirical formula: C17H20N2O) is a gunshot residue also known as ethyl centralite. Its IUPAC name is 1,3-diethyl-1,3-diphenylurea. Ethyl centralite is insoluble in water, but is soluble in acetone, ethanol and benzene.
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