![]() Methyl trichloroacetate structure
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Common Name | Methyl trichloroacetate | ||
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CAS Number | 598-99-2 | Molecular Weight | 177.414 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 147.9±3.0 °C at 760 mmHg | |
Molecular Formula | C3H3Cl3O2 | Melting Point | -18°C | |
MSDS | Chinese USA | Flash Point | 72.8±0.0 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Stable chlorine isotope analysis of chlorinated acetic acids using gas chromatography/quadrupole mass spectrometry.
Rapid Commun. Mass Spectrom. 29 , 2341-8, (2015) The environmental occurrence of chlorinated acetic acids (CAAs) has been extensively studied, but the sources and transport are still not yet fully understood. A promising approach for source apportionment and process studies is the isotopic characterization ... |
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Negative staining of proteins in polyacrylamide gels with methyl trichloroacetate.
Anal. Biochem. 243(2) , 245-8, (1996) This paper describes a new, sensitive (in the nanogram range), and rapid (two-step) technique for the negative staining of proteins in polyacrylamide gels in the presence or absence of sodium dodecyl sulfate. After separation, gels are incubated with 8% methy... |
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Methyl chloroacetate as an extraction solvent for coupling liquid-liquid semimicroextraction with micellar electrokinetic chromatography through on-capillary decomposition for the separation of neutral compounds with concentration enhancement.
J. Chromatogr. A. 1147(1) , 105-10, (2007) This paper reports the use of methyl chloroacetate (MCA) as an extraction solvent for coupling liquid-liquid semimicroextraction (LLsME) with micellar electrokinetic chromatography (MEKC) through on-capillary decomposition for the separation of neutral compou... |
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Synthesis and anticonvulsant activity of O-alkylated derivatives of 1-(2-naphthyl)-2-(imidazol-1-yl)ethanone oxime.
Arzneimittelforschung 62(9) , 420-4, (2012) In this study, O-alkylated derivatives of nafimidone oxime chemically, 1-(2-naphthyl)-2-(imidazol-1-yl)ethanone oxime have been synthesized as potential anticonvulsant compounds. O-alkylation of the oxime using hydrochlorides of various dialkylaminoethyl chlo... |
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