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Merck
CN

49049

γ-六六六

PESTANAL®, analytical standard

别名:

林丹, γ-BHC, 1α,2α,3β,4α,5α,6β-六氯环己烷

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关于此项目

经验公式(希尔记法):
C6H6Cl6
化学文摘社编号:
分子量:
290.83
EC Number:
200-401-2
UNSPSC Code:
41121813
PubChem Substance ID:
Beilstein/REAXYS Number:
1907337
MDL number:
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InChI key

JLYXXMFPNIAWKQ-GNIYUCBRSA-N

InChI

1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H/t1-,2-,3-,4+,5+,6+

SMILES string

Cl[C@H]1[C@H](Cl)[C@H](Cl)[C@@H](Cl)[C@H](Cl)[C@@H]1Cl

grade

analytical standard

product line

PESTANAL®

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

113-115 °C (lit.)

application(s)

agriculture
environmental

format

neat

storage temp.

2-30°C

Gene Information

mouse ... Esr1(13982)
rat ... Ar(24208)

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Application

Product 49049 has been discontinued. Product 45548-250MG may be an acceptable replacement.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Lact. - STOT RE 2

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

监管及禁止进口产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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L A Videla et al.
Free radical biology & medicine, 9(2), 169-179 (1990-01-01)
The development of an oxidative stress condition in the liver by lindane intoxication is discussed as a possible hepatotoxic mechanism of the insecticide. Lindane is metabolized by liver microsomal enzymes to a variety of metabolites, which are susceptible of conjugation
Yuji Nagata et al.
Applied microbiology and biotechnology, 76(4), 741-752 (2007-07-20)
gamma-Hexachlorocyclohexane (gamma-HCH, also called gamma-BHC and lindane) is a halogenated organic insecticide that causes serious environmental problems. The aerobic degradation pathway of gamma-HCH was extensively revealed in bacterial strain Sphingobium japonicum (formerly Sphingomonas paucimobilis) UT26. gamma-HCH is transformed to 2,5-dichlorohydroquinone
Microbial degradation of the pesticide lindane (gamma-hexachlorocyclohexane).
B K Singh et al.
Advances in applied microbiology, 47, 269-298 (2003-07-25)
John Vijgen et al.
Environmental science and pollution research international, 18(2), 152-162 (2010-11-26)
Hexachlorocyclohexane (HCH) isomers (α-, β- and γ- (Lindane)) were recently included as new persistent organic pollutants (POPs) in the Stockholm Convention, and therefore, the legacy of HCH and Lindane production became a contemporary topic of global relevance. This article wants
R M Joy
Neurobehavioral toxicology and teratology, 4(6), 813-823 (1982-11-01)
A mode of action for lindane, dieldrin and related chlorinated hydrocarbon insecticides is proposed. The available evidence suggests that these insecticides act upon neurons in a global manner. Their primary target is the synapse, and they act there to intensify

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