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47278

Supelco

Bromodichloroacetic acid solution

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

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About This Item

Empirical Formula (Hill Notation):
C2HBrCl2O2
CAS Number:
71133-14-7
Molecular Weight:
207.84
EC Number:
216-653-1
UNSPSC Code:
12000000

grade

certified reference material
TraceCERT®

agency

EPA 552.2

product line

TraceCERT®

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

InChI

1S/C2HBrCl2O2/c3-2(4,5)1(6)7/h(H,6,7)

InChI key

XSWVFEQKZFUULO-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.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

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_germany

WGK 1

flash_point_f

-18.4 °F - closed cup

flash_point_c

-28 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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William M Gwinn et al.
Toxicological sciences : an official journal of the Society of Toxicology, 176(2), 343-354 (2020-06-04)
A 5-day in vivo rat model was evaluated as an approach to estimate chemical exposures that may pose minimal risk by comparing benchmark dose (BMD) values for transcriptional changes in the liver and kidney to BMD values for toxicological endpoints
J L Merdink et al.
Journal of applied toxicology : JAT, 21(1), 53-57 (2001-02-17)
The oral and i.v. elimination kinetics were investigated for bromodichloroacetate (BDCA), a haloacetate found in drinking water. The BDCA was administered at a dose of 5, 20 and 100 mg kg-1 to B6C3F1 mice and appears to distribute to the
E W Austin et al.
Journal of toxicology and environmental health, 52(4), 367-383 (1997-11-14)
Haloacetates are a common class of water chlorination by-products. Depending on the amount of bromide in the source water, varying amounts of chlorinated, brominated, and mixed bromochloro haloacetates are produced. When administered to rodents, haloacetates have been shown to increase
G Xu et al.
Drug metabolism and disposition: the biological fate of chemicals, 23(12), 1412-1416 (1995-12-01)
Trichloroacetate (TCA), dichloroacetate (DCA), and bromodichloroacetate (BDCA) are byproducts of the chlorination of drinking water. TCA acts primarily as a peroxisome proliferator, but DCA produces tumors at doses less than required for peroxisome proliferation. BDCA does not induce peroxisome proliferation
V Lopez-Avila et al.
Journal of AOAC International, 82(3), 689-704 (1999-06-15)
The microextraction/ion chromatographic (IC) method developed in this study involves extraction of 9 haloacetic acids (HAAs) from aqueous samples (acidified with sulfuric acid to a pH of < 0.5 and amended with copper sulfate pentahydrate and sodium sulfate) with methyl
View All Related Papers

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