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ALPHA-HCH

Product Name
ALPHA-HCH
CAS No.
319-84-6
Chemical Name
ALPHA-HCH
Synonyms
A-BHC;ALPHA-BHC;ALPHA-HEXACHLOROCYCLOHEXANE;Hexachlorcyclohexan;α-Hexachlorocyclohexane;r-1,c-2,t-3,c-4,t-5,t-6-hexachlorocyclohexane;a-HCH;ent9,232;ALPHA-HCH;ENT 9,232
CBNumber
CB4345259
Molecular Formula
C6H6Cl6
Formula Weight
290.81
MOL File
319-84-6.mol
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ALPHA-HCH Property

Melting point:
156-161 °C(lit.)
Boiling point:
373.64°C (rough estimate)
Density 
1.9 g/cm3
vapor pressure 
173 at 25 °C (subcooled liquid vapor pressure calculated from GC retention time data, Hinckley etal., 1990)
refractive index 
1.60-1.626 (589.3 nm 20℃)
Flash point:
11 °C
storage temp. 
APPROX 4°C
solubility 
Soluble in ethanol, benzene, chloroform (Weast, 1986), cod liver oil, and octanol (Montgomery, 1993)
form 
Solid
color 
White
Water Solubility 
2mg/L(25 ºC)
BRN 
7073451
Henry's Law Constant
0.888 at 5 °C, 1.58 at 15 °C, 2.27 at 20 °C, 2.96 at 25 °C, 6.02 at 35 °C:in 3% NaCl solution: 1.48 at 5 °C, 2.76 at 15 °C, 5.23 at 25 °C, 7.20 at 35 °C (gas stripping-GC, Cetin et al., 2006)
Stability:
Stable. Incompatible with strong oxidizing agents.
EPA Substance Registry System
.alpha.-Hexachlorocyclohexane (319-84-6)
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Safety

Hazard Codes 
T,N,F
Risk Statements 
21-25-40-50/53-39/23/24/25-23/24/25-11-52/53
Safety Statements 
22-36/37-45-60-61-16-7
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
GV3500000
HazardClass 
6.1(b)
PackingGroup 
III
Hazardous Substances Data
319-84-6(Hazardous Substances Data)
Toxicity
LC50 (96-hour) for guppies >1.4 mg/L (Verschueren, 1983); acute oral LD50 for rats 177 mg/kg (RTECS, 1985).
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H312Harmful in contact with skin

H351Suspected of causing cancer

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P202Do not handle until all safety precautions have been read and understood.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
33856
Product name
α-HCH
Purity
PESTANAL
Packaging
50mg
Price
$108
Updated
2024/03/01
Sigma-Aldrich
Product number
40100-U
Product name
α-BHC solution
Purity
certified reference material, 1000?μg/mL in methanol
Packaging
1mL
Price
$34.6
Updated
2022/05/15
TRC
Product number
H290775
Product name
α-1,2,3,4,5,6-Hexachlorocyclohexane(>90%)
Packaging
2.5g
Price
$1250
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
70464
Product name
α-1,2,3,4,5,6-Hexachlorocyclohexane
Packaging
1g
Price
$2080
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
PST0000766
Product name
1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE ALPHA-ISOMER
Purity
95.00%
Packaging
10MG
Price
$952.01
Updated
2021/12/16
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ALPHA-HCH Chemical Properties,Usage,Production

Description

BHC is a white-to-brownish crystalline solid witha musty, phosgene-like odor. Molecular weight = 290.82;Freezing/Melting point = 65℃. Hazard Identification (basedon NFPA-704 M Rating System): Health 2, Flammability 1,Reactivity 0. BCH consists of eight stereoisomers of which thegamma(~) isomer is most insecticidally active and hence mostimportant. See also“Lindane.”

Chemical Properties

BHC is a white-to-brownish crystalline solid with a musty, phosgene-like odor.

Physical properties

Brownish to white monoclinic prisms, crystalline solid or powder with a phosgene-like odor (technical grade). An odor threshold concentration of 88 μg/kg was reported by Sigworth (1964).

Uses

Not produced commercially in the U.S. and its sale is prohibited by the U.S. EPA.

Uses

α-1,2,3,4,5,6-Hexachlorocyclohexane is an organochloride which is one of the isomers of hexachlorocyclohexane and is an byproduct of insecticide Lindane (L465990).

Definition

ChEBI: 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 Description

White crystalline powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Halogenated aliphatic compounds, such as ALPHA-HCH, are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

Health Hazard

ACUTE/CHRONIC HAZARDS: Carcinogen. Toxic. Irritant. Hazardous decomposition product.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Safety Profile

ConfEmed carcinogen with experimental carcinogenic, tumorigenic, and neoplastigenic data. Poison by ingestion. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl-. See also BENZENE HEXACHLORIDE and other benzenehexachloride entries.

Potential Exposure

The 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.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least30 min, occasionally lifting upper and lower lids. Seek med-ical ;attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Speed in removing material from skinis of extreme importance. Shampoo hair promptly if con-taminated. Seek medical attention immediately. If thischemical has been inhaled, remove from exposure, beginrescue ;breathing (using universal precautions, includingresuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medi-cal attention. Give large quantities of waterand inducevomiting. Do not make an unconscious person vomit.

Environmental Fate

Biological. Clostridium sphenoides degraded α-BHC to δ-3,4,5,6-tetrachloro-1-cyclo hexane (Heritage and MacRae, 1977a). In four successive 7-day incubation periods, α- BHC (5 and 10 mg/L) was recalcitrant to degradation in a settled domestic wastewater inoculum (Tabak et al., 1981).
Soil. Under aerobic conditions, indigenous microbes in contaminated soil produced pentachlorocyclohexane. However, under methanogenic conditions, α-BHC was converted to chlorobenzene, 3,5-dichlorophenol and the tentatively identified compound 2,4
Photolytic. When an aqueous solution containing α-BHC was photooxidized by UV light at 90–95°C, 25, 50 and 75% degraded to carbon dioxide after 4.2, 24.2 and 40.0 hours, respectively (Knoevenagel and Himmelreich, 1976). In basic, aqueous solution
Chemical/Physical. Emits very toxic chloride fumes when heated to decomposition (Lewis, 1990). α-BHC will hydrolyze via trans-dehydrochlorination of the axial chlorines resulting in the formation of hydrochloric acid and the intermediate 1,3,4,5,6-pentachlo rocyclo-hexene. The intermediate will undergo further hydrolysis resulting in the formation of 1,2,3-trichlorobenzene, 1,2,4-trichlorobenzene and hydrochloric acid (Kollig, 1993).

storage

Color Code- Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Store in tightly closed containers in a cool, well-ventilated area away from alkalis, powdered iron, alumi-num, and zinc. Where possible, automatically pump liquidfrom drums or other storage containers to process contain-ers. A regulated, marked area should be established wherethis chemical is handled, used, or stored in compliance withOSHA Standard 1910.1045.

Shipping

UN2761 Organochlorine pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods

Crystallise it from EtOH. Purify it also by zone melting. Possible CANCER AGENT, TOXIC. [: Beilstein 1 H 23, : Beilstein 5 I 8, many isomers : Beilstein 5 III 41, 5 IV 55.]

Incompatibilities

Incompatible 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 Disposal

A 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.

ALPHA-HCH Preparation Products And Raw materials

Raw materials

Preparation Products

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ALPHA-HCH Suppliers

Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22514
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Codow Chemical Co.,Ltd.
Tel
18620099427 18620099427
Fax
+86-20-62619665
Email
amy@howeipharm.com
Country
China
ProdList
1751
Advantage
55
Shanghai Xilong Biochemical Technology Co., Ltd.
Tel
021-52907766-8042
Fax
021-52906523
Country
China
ProdList
9941
Advantage
58
Grader reagent
Tel
18221735425
Email
sales@xinpingchem.com
Country
China
ProdList
9942
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
021-021-52271985 17721149837
Fax
+86 (21) 52271987
Email
sales@9dingchem.com
Country
China
ProdList
19800
Advantage
60
Shanghai BaiShun Biological Technology Co., Ltd
Tel
021-37581181
Fax
021-57456066
Email
sales@chem-mall.com
Country
China
ProdList
10330
Advantage
58
Rhawn Reagent
Tel
400-400-1332688 18019345275
Fax
400-133-2688
Email
amy@rhawn.cn
Country
China
ProdList
15497
Advantage
58

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