36548
Methyl trichloroacetate
PESTANAL®, analytical standard
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About This Item
Linear Formula:
CCl3CO2CH3
CAS Number:
Molecular Weight:
177.41
EC Number:
209-960-7
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1756075
MDL number:
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.455 (lit.)
bp
152-153 °C (lit.)
density
1.488 g/mL at 25 °C (lit.)
application(s)
agriculture
environmental
format
neat
SMILES string
COC(=O)C(Cl)(Cl)Cl
InChI
1S/C3H3Cl3O2/c1-8-2(7)3(4,5)6/h1H3
InChI key
VHFUHRXYRYWELT-UHFFFAOYSA-N
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
161.6 °F - closed cup
flash_point_c
72 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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G Candiano et al.
Analytical biochemistry, 243(2), 245-248 (1996-12-15)
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% methyl
Tianlin Wang et al.
Journal of chromatography. A, 1147(1), 105-110 (2007-03-03)
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 compounds with concentration enhancement. Alkylphenones of C(8), C(10) and
R Bansal et al.
Arzneimittel-Forschung, 62(9), 420-424 (2012-07-14)
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 chlorides, methyl chloroacetate and alkyl dihalides gave the O-alkylated derivatives. Anticonvulsant activity of