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Merck
CN

48103

毒杀芬 溶液

certified reference material, 1000 μg/mL in isooctane

别名:

氯化莰 溶液

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化学文摘社编号:
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.24
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SMILES string

ClC21C(C(C(C2Cl)Cl)(C(=C)C1(CCl)CCl)Cl)(Cl)Cl

InChI

1S/C10H8Cl8/c1-4-7(2-11,3-12)9(16)6(14)5(13)8(4,15)10(9,17)18/h5-6H,1-3H2

InChI key

OEJNXTAZZBRGDN-UHFFFAOYSA-N

grade

certified reference material, TraceCERT®

agency

EPA 8081

product line

TraceCERT®

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 1 mL

concentration

1000 μg/mL in isooctane

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-30°C

Quality Level

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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

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

10.4 °F - closed cup

flash_point_c

-12 °C - closed cup

法规信息

监管及禁止进口产品
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Shaoqiong Tian et al.
Se pu = Chinese journal of chromatography, 30(1), 14-20 (2012-06-07)
A novel method for the determination of representative toxaphene congeners in traditional Chinese herbal medicines was developed. Ginseng and Milkvetch Root were selected as the samples and seven toxaphene congeners were selected as the monitoring objects. The samples were extracted
Thomas Kapp et al.
Chemosphere, 82(1), 32-36 (2010-11-13)
For decades, toxaphene had been used as a major chloropesticide. Degradation of the multicomponent mixture in the environment was mainly reported to be due to anaerobic dechlorination and hydrodechlorination. Little was known about oxidative transformation processes and the potential hydroxylated
Seonock Woo et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 156(1), 37-41 (2012-04-14)
We evaluated toxaphene-induced acute toxicity in Hydra magnipapillata. The median lethal concentrations of the animals (LC(50)) were determined to be 34.5 mg/L, 25.0 mg/L and 12.0 mg/L after exposure to toxaphene for 24 h, 48 h and 72 h, respectively.
M H G Berntssen et al.
Aquatic toxicology (Amsterdam, Netherlands), 112-113, 54-61 (2012-03-01)
The relative feed-to-fish accumulation and possible biotransformation of the nona-chlorinated toxaphene congeners currently included in EU-legislation (CHB-50 and -62) and the octa-chlorinated congeners recommended by the European Food Safety Authority to be included in future surveillance of fish samples (CHB-40
Juan José Alava et al.
Environmental toxicology and chemistry, 30(7), 1677-1688 (2011-04-22)
Persistent organic pollutants (POPs) are recognized manmade threats to sea turtle populations, but substantial uncertainty exists surrounding their exposure to contaminants and their sensitivity to toxic effects. This uncertainty creates difficulty for conservation managers to make informed decisions for the

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