nitrosyl chloride

nitrogen oxychloride

CAS: 2696-92-6 Cl N O MW: 65.45820000

Identification

Namenitrosyl chloride
CAS Number2696-92-6
EINECS220-273-1
FDA UNIINHE5I1E5H6
Molecular FormulaCl N O
Molecular Weight65.45820000
Nikkaji NumberJ31.850G

Regulatory

FDA Mainterm (SATF)2696-92-6 ; NITROSYL CHLORIDE
FDA RegulationFDA PART 137 -- CEREAL FLOURS AND RELATED PRODUCTS

Physical Properties

Food Chemicals Codex Listed No
Boiling Point -5.50 °C. @ 760.00 mm Hg (est)
Vapor Pressure 2180.135986 mmHg @ 25.00 °C. (est)
Flash Point 32.00 °F. TCC ( 0.00 °C. ) (est)
logP (o/w) 0.351 (est)
Soluble in water, 1.124e+005 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorybleaching agents or flour-maturing agents
Recommendation for nitrosyl chloride usage levels up tonot for fragrance use.
Recommendation for nitrosyl chloride flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

nitrogen chloride oxide nitrogen oxychloride nitrogen oxychloride (NOCl) nitrosonium chloride nitrosyl chloride ((NO)Cl) nitrosyl chloride [UN1069] [Poison gas] PubMed: NEXAFS and XPS studies of nitrosyl chloride. PubMed: Synthesis and Properties of Heavy Chalcogen Analogues of the Texas Reds and Related Rhodamines. PubMed: Ruthenium-nitrosyl complexes with glycine, L-alanine, L-valine, L-proline, D-proline, L-serine, L-threonine, and L-tyrosine: synthesis, X-ray diffraction structures, spectroscopic and electrochemical properties, and antiproliferative activity. PubMed: Electronic tuning of nitric oxide release from manganese nitrosyl complexes by visible light irradiation: enhancement of nitric oxide release efficiency by the nitro-substituted quinoline ligand. PubMed: Reaction of a copper(II)-nitrosyl complex with hydrogen peroxide: phenol ring nitration through a putative peroxynitrite intermediate. 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