butyl chloroformate

carbonochloridic acid, butyl ester

CAS: 592-34-7 C5 H9 Cl O2 MW: 136.57713000

Identification

Namebutyl chloroformate
IUPACbutyl carbonochloridate
CAS Number592-34-7
EINECS209-750-5
FDA UNIISearch
Molecular FormulaC5 H9 Cl O2
Molecular Weight136.57713000
MDL NumberMFCD00000650
Nikkaji NumberJ95.611B
Beilstein0605635
XlogP32.80 (est)

Regulatory

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 1.07400 @ 25.00 °C.
Boiling Point 142.00 °C. @ 760.00 mm Hg
Vapor Pressure 5.895000 mmHg @ 25.00 °C. (est)
Flash Point 77.00 °F. TCC ( 25.00 °C. )
logP (o/w) 1.895 (est)
Soluble in water, 3654 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
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

Categorypharmaceuticals / chemical synthisis
Recommendation for butyl chloroformate usage levels up tonot for fragrance use.
Recommendation for butyl chloroformate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

butyl carbonochloridate butyl chlorocarbonate N- butyl chloroformate N- butyl chloroformate [UN2743] [Poison] butylchloroformate carbonochloridic acid butyl ester carbonochloridic acid, butyl ester chloroformic acid butyl ester chloroformic acid N-butyl ester formic acid, chloro-, butyl ester PubMed: Gas chromatographic determination of some phenolic compounds in fuels and engine oil after simultaneous derivatization and microextraction. PubMed: Effects of derivatization reagents consisting of n-alkyl chloroformate/n-alcohol combinations in LC-ESI-MS/MS analysis of zwitterionic antiepileptic drugs. PubMed: Correlation of the rates of solvolysis of tert-butyl chlorothioformate and observations concerning the reaction mechanism. PubMed: In-sample derivatization-solid-phase microextraction of amphetamines and ecstasy related stimulants from water and urine. PubMed: Syntheses and detailed structure characterization of dextran carbonates. PubMed: Quantitative liquid chromatography-tandem mass spectrometry profiling of activated methyl cycle metabolites involved in LuxS-dependent quorum sensing in Escherichia coli. PubMed: Derivatisation in gas chromatographic determination of acidic herbicides in aqueous environmental samples. PubMed: 4-(6-methoxy-2-naphthyl)-2-butyl chloroformate enantiomers: new reagents for the enantiospecific analysis of amino compounds in biogenic matrices. PubMed: Synthesis and calcium channel antagonist activity of dialkyl 4- (dihydropyridinyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinecarboxylates.