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Merck
CN

40103-U

δ-BHC

certified reference material, 1000 μg/mL in methanol

Synonym(s):

δ-HCH solution, δ-1,2,3,4,5,6-Hexachlorocyclohexane solution

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About This Item

Empirical Formula (Hill Notation):
C6H6Cl6
CAS Number:
319-86-8
Molecular Weight:
290.83
MDL number:
MFCD00003825
UNSPSC Code:
77101502
NACRES:
NA.24

Key Documents

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SMILES string

ClC1C(C(C(C(C1Cl)Cl)Cl)Cl)Cl

InChI

1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H

InChI key

JLYXXMFPNIAWKQ-UHFFFAOYSA-N

grade

certified reference material, TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

1000 μg/mL in methanol

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

2-8°C

Quality Level

300

Related Categories

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

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

Certificates of Analysis (COA)

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Ai-zhi Ma et al.
Wei sheng wu xue bao = Acta microbiologica Sinica, 45(5), 728-732 (2005-12-14)
An aerobic bacterium was isolated successfully from a long-term contaminated upland field, which was named BHC-A. The bacterium can utilize Hexachlorocycloexane as a sole carbon source and decompose this substance rapidly and completely. According to its physiological & biochemical characters
D Belelli et al.
British journal of pharmacology, 127(3), 601-604 (1999-07-13)
Many structurally diverse general anaesthetics enhance inhibitory neurotransmission in the central nervous system by interacting with the GABAA receptor. By contrast, GABA receptors composed of the rho 1 subunit are anaesthetic-insensitive. Here, we demonstrate that both delta-hexachlorocyclohexane (delta-HCH; 1-100 microM)
S N Wu et al.
Molecular pharmacology, 57(5), 865-874 (2000-04-25)
delta-Hexachlorocyclohexane (delta-HCH), a lipophilic neurodepressant agent, has been shown to inhibit neurotransmitter release and stimulate ryanodine-sensitive Ca(2+) channels. However, the effect of delta-HCH on neuronal activity remains unclear, although it may enhance the gamma-aminobutyric acid-induced current. Its effects on ionic
Zhaojie Cui et al.
Journal of bioscience and bioengineering, 113(6), 765-770 (2012-02-14)
The reductive biotransformation of α-, β-, γ-, and δ-hexachlorocyclohexane isomers was investigated using five alternative electron donors (i.e., glucose plus methanol, glucose only, methanol only, acetate, and ethanol) in a batch assay of an HCH-dechlorinating anaerobic culture. In addition, a
G S Toteja et al.
Food additives and contaminants, 23(3), 281-288 (2006-04-21)
Under a multicentre study conducted by the Indian Council of Medical Research, 1712 samples of wheat grain/flour were collected from urban and rural areas in 11 states representing different geographical regions of India. These samples were analysed for residues of
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