Chloropicrin
Structural Formula Vector Image
Title: Chloropicrin
CAS Registry Number: 76-06-2
CAS Name: Trichloronitromethane
Additional Names: acquinite; nitrochloroform
Trademarks: Larvacide 100; Picfume (Dow)
Molecular Formula: CCl3NO2
Molecular Weight: 164.38
Percent Composition: C 7.31%, Cl 64.70%, N 8.52%, O 19.47%
Literature References: First prepd in 1848 by Stenhouse from picric acid and bleach powder. Review of prepn, properties, physiological action, and uses: Jackson, Chem. Rev. 14, 251 (1934). Manuf from nitromethane and alkaline hypochlorite: Wilhelm, US 3106588 (1963).
Properties: Slightly oily liquid, intense odor; bp757 112°. mp -64°; mp -69.2° (corr). d420 1.6558, d425 1.6483. nD20 1.4611, nD25 1.4596. Dipole moment in heptane or benzene, 1.80D. Practically insol in water. Soly in water (g/100 ml): 0.2272 (0°), 0.1621 (25°). Miscible with benzene, abs alc, carbon disulfide; sol in ether.
Melting point: mp -64°; mp -69.2° (corr)
Boiling point: bp757 112°
Index of refraction: nD20 1.4611; nD25 1.4596
Density: d420 1.6558; d425 1.6483
CAUTION: Potential symptoms of overexposure are irritation of eyes, skin, respiratory system; lacrimation; cough, pulmonary edema; nausea, vomiting. See NIOSH Pocket Guide to Chemical Hazards (DHHS/NIOSH 97-140, 1997) p 66.
Use: Disinfecting cereals and grains; in synthesis, esp in manuf of methyl violet; fumigant; soil insecticide; war gas.

Other Monographs:
DimethisoquinAcetyldigitoxinsTEMPOLAmsacrine
MoexiprilVoacamineVitamin(s) LAgaric
PerfosfamideColchiceineTianeptineMethixene
1-NaphthalenethiolMelezitoseOrnoprostilKoser's Reagent
©2006-2023 DrugFuture->Chemical Index Database