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Merck
CN

47654-U

Chloroacetic acid solution

certified reference material, 1000 μg/mL in methyl tert-butyl ether

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About This Item

CAS Number:
79-11-8
UNSPSC Code:
77101502
NACRES:
NA.24

Key Documents

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InChI

1S/C2H3ClO2/c3-1-2(4)5/h1H2,(H,4,5)

InChI key

FOCAUTSVDIKZOP-UHFFFAOYSA-N

grade

certified reference material, TraceCERT®

agency

EPA 552.2

product line

TraceCERT®

form

liquid

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 1 mL

concentration

1000 μg/mL in methyl tert-butyl ether

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°C

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

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H315

Hazard Classifications

Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

-27.4 °F - closed cup

flash_point_c

-33.0 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

监管及禁止进口产品
This item has

Certificates of Analysis (COA)

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Maike M Schmidt et al.
Neurotoxicity research, 19(4), 628-637 (2010-07-16)
The chlorinated acetates monochloroacetate (MCA), dichloroacetate (DCA), and trichloroacetate (TCA) are generated in water disinfection processes and are formed during metabolic detoxification of industrial solvents such as trichloroethylene. In order to test for consequences of an exposure of brain cells
Qian Xu et al.
Huan jing ke xue= Huanjing kexue, 32(7), 1967-1973 (2011-09-20)
Twelve typical nitrogenous organic compounds including herbicides, pesticides, amino acids, industrial products etc in polluted raw water were selected to investigate formation of typical carbonaceous and nitrogenous DBPs during chlorination and chloramination. To indentify the formation mechanism of carbonaceous and
Khalid Alhooshani et al.
Talanta, 86, 109-113 (2011-11-09)
For the first time, haloacetic acids and aromatic acetic acids were extracted from wastewater samples using electromembrane extraction (EME). A thin layer of toluene immobilized on the walls of a polypropylene membrane envelope served as an artificial supported liquid membrane
Rosanne Slingsby et al.
Journal of chromatographic science, 47(7), 523-528 (2009-09-24)
This paper presents the determination of nine haloacetic acids (HAAs) in high ionic strength, treated effluent waters using an ion chromatography-electrospray ionization-tandem mass spectrometry (IC-ESI-MS-MS) method with internal standards and discussions of each of the method parameters. Data is also
Xianbin Su et al.
BMC microbiology, 12, 267-267 (2012-11-22)
Acetate is a commonly used substrate for biosynthesis while monochloroacetate is a structurally similar compound but toxic and inhibits cell metabolism by blocking the citric acid cycle. In Burkholderia species MBA4 haloacetate was utilized as a carbon and energy source
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