LINDANE

LINDANE Basic information
Product Name:LINDANE
Synonyms:1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE, GAMMA-ISOMER;1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE [G-ISOMER];Cyclohexane, 1,2,3,4,5,6-hexachloro-, delta-;Cyclohexane, 1,2,3,4,5,6-hexachloro-, delta-isomer;Cyclohexane, delta,1,2,3,4,5,6-hexachloro-;cyclohexane,1,2,3,4,5,6-hexachloro-,(1alpha,2alpha,3alpha,4beta,5alpha,6;Cyclohexane,1,2,3,4,5,6-hexachloro-,(1-α,2-α,3-α,4-β,5-α,6-β)-;cyclohexane,1,2,3,4,5,6-hexachloro-,(1α,2α,3α,4β,5α,6β)-
CAS:319-86-8
MF:C6H6Cl6
MW:290.83
EINECS:206-272-9
Product Categories:Pesticides&Metabolites;Alphabetic;A-BAlphabetic;Alpha sort;B;BA - BH
Mol File:319-86-8.mol
LINDANE Structure
LINDANE Chemical Properties
Melting point 113-115 °C(lit.)
Boiling point 373.64°C (rough estimate)
density 1.7152 (rough estimate)
vapor pressure 3.52 at 25 °C (Banerjee et al., 1990)
refractive index 1.576-1.674 (589.3 nm 20℃)
Fp 11 °C
storage temp. 2-8°C
solubility Soluble in ethanol, benzene, and chloroform (Weast, 1986)
form Solid
BRN 1907334
Henry's Law Constant(x 10-7 atm·m3/mol): 2.5 at 20 °C (approximate - calculated from water solubility and vapor pressure)
EPA Substance Registry System.delta.-Hexachlorocyclohexane (319-86-8)
Safety Information
Hazard Codes T,N,F,Xn
Risk Statements 20/21-25-48/22-50/53-64-39/23/24/25-23/24/25-11-40-21-67-65-38-52/53
Safety Statements 36/37-45-60-61-22-16-7-62
RIDADR UN 2811 6.1/PG 1
WGK Germany 3
RTECS GV4900000
Hazardous Substances Data319-86-8(Hazardous Substances Data)
ToxicityAcute oral LD50 for rats 1,000 mg/kg (RTECS, 1985).
MSDS Information
ProviderLanguage
SigmaAldrich English
LINDANE Usage And Synthesis
Chemical PropertiesBHC is a white-to-brownish crystalline solid with a musty, phosgene-like odor.
Physical propertiesSolid crystals or fine platelets with a faint musty-like odor
UsesInsecticide.
Usesδ-1,2,3,4,5,6-Hexachlorocyclohexane is an organochloride annd is one of the isomers of hexachlorocyclohexane. aδ-1,2,3,4,5,6-Hexachlorocyclohexane is also an byproduct of insecticide Lindane (L465990) .
DefinitionChEBI: Beta-hexachlorocyclohexane is the beta-isomer of hexachlorocyclohexane. It has a role as a persistent organic pollutant. It is an organochlorine pesticide and a hexachlorocyclohexane.
General DescriptionSlightly musty odor.
Reactivity ProfileLINDANE may be incompatible with strong oxidizing and reducing agents. Incompatible with some amines, nitrides, azo/diazo compounds, with alkali metals, and with epoxides.
Health HazardACUTE/CHRONIC HAZARDS: Highly toxic. May cause irritation on contact. Hazardous decomposition products.
Potential ExposureThe major commercial usage of BHC is based upon its insecticidal properties. α-BCH is used as an Agricultural chemical, pesticide, pharmaceutical, and veterinary drug. The 7-isomer has the highest acute toxic ity, but the other isomers are not without activity. It is gen erally advantageous to purify the 7-isomer from the less active isomers. The γ-isomer acts on the nervous system of insects, principally at the level of the nerve ganglia. As a result, lindane has been used against insects in a wide range of applications including treatment of animals, buildings, humans for ectoparasites, clothes; water for mosquitoes; living plants; seeds and soils. Some applications have been abandoned due to excessive residues, e.g., stored food stuffs. By voluntary action, the principal domestic producer of technical grade BHC requested cancellation of its BHC registrations on September 1, 1976. As of July 21, 1978, all registrants of pesticide products containing BHC voluntar ily canceled their registrations or switched their former BHC products to lindane formulations.
Environmental FateBiological. Dehydrochlorination of δ-BHC by a Pseudomonas sp. under aerobic con ditions was reported by Sahu et al. (1992). They also reported that when deionized water containing δ-BHC was inoculated with Pseudomonas sp., the concentration of δ-BHC decreased to undetectable levels after 8 days with concomitant formation of chloride ions and δ-pentachlorocyclohexane. In four successive 7-day incubation periods, δ-BHC (5 and 10 mg/L) was recalcitrant to degradation in a settled domestic wastewater inoculum (Tabak et al., 1981).
Chemical/Physical. δ-BHC dehydrochlorinates in the presence of alkalies. The hydrol ysis half-lives at pH values of 7 and 9 are 191 days and 11 hours, respectively (Worthing and Hance, 1991).
ShippingUN2761 Organochlorine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
IncompatibilitiesIncompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explo sions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Decomposes on contact with powdered iron, aluminum, zinc, and on contact with strong bases producing trichlorobenzene.
Waste DisposalA process has been developed for the destructive pyrolysis of benzene hexachloride @ 400 500℃ with a catalyst mixture which contains 5 10% of either cupric chloride, ferric chloride; zinc chloride; or aluminum chloride on activated carbon.
LINDANE Preparation Products And Raw materials
LINDANE (BHC GAMMA ISOMER) SOLUTION 100UG/ML IN TOLUENE 5ML LINDANE SOLUTION 100UG/ML IN ACETONITRILE 1ML (g-Benzenehexachloride) (g-BHC) (Lindane-D6),GAMMA-1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE-D6 BHC (DELTA ISOMER) (13C6) Parathion+BCH,powder LINDANE (BHC GAMMA ISOMER) (13C6) SOLUTION 100UG/ML IN N-NONANE 1.2ML ALPHA-HCH SOLUTION 100 NG/MYL IN METHAN& MIREX (13C8) Trichlorphon+BCH,powder (5.5%) ORGANOCHLORINE PESTICIDE MATRIX SPIKING MIXTURE LINDANE (BHC GAMMA ISOMER) (13C6, D6) SOLUTION 100UG/ML IN N-NONANE 1.2ML BCH+Parathion-methyl,powder LINDANE (13C6, D6) CHLORDECONE HYDRATE LINDANE (BHC GAMMA ISOMER) SOLUTION 100UG/ML IN TOLUENE 5X1ML LINDANE-UL-14C GAMMA-HCH D6 LINDANE (13C6)

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