| Identification | Back Directory | [Name]
BETA-HCH | [CAS]
319-85-7 | [Synonyms]
B-BHC
hc beta
ent9,233
BETA-HCH
BETA-BHC
beta-666
ENT 9,233
BHC(beta)
betaisomer
beta-Lindane
beta-HCH (BHC)
β-BHC standard
beta-hexachloran
BHC (BETA ISOMER)
beta-HCH solution
beta-hch (bsi,iso)
beta-bhc (jmaf,iso)
beta-BHC (beta-HCH)
β-BHC solution,10ppm
BETA-BHC, 50MG, NEAT
β-BHC solution,1000ppm
beta-hexachlorobenzene
-HCH PESTANAL
BETA-BENZENEHEXACHLORIDE
BETA-HEXACHLOROCYCLOHEXANE
β-HCH standard in isooctane
Hexachlorocyclohexane - beta
BHC BETA ISOMER, 100MG, NEAT
BETA-BHC, 1X1ML, MEOH, 20UG/ML
trans-alpha-Benzenehexachloride
BETA-BHC, 1X1ML, ACET, 1000UG/ML
b-HCH
HEXACHLOROCYCLOHEXANE-BETAISOMER
BHC (beta isomer) 100mg [319-85-7]
β-HCH solution, 20 μg/mL in methanol
β-HCH solution,1000 μg/mL in acetone
2,3,4,5,6-hexachloro-beta-cyclohexan
2,3,4,5,6-hexachloro-trans-cyclohexan
BETA-1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE
beta-1,2,3,4,5,6-hexachloro-cyclohexan
cyclohexane,1,2,3,4,5,6-hexachloro-,β-
Cyclohexane, beta-1,2,3,4,5,6-hexachloro-
1,2,3,4,5,6-Hexzchlorocyclohexane,-isomer
b-benzenehexachloridestandardforepamethods
Cyclohexane, 1,2,3,4,5,6-hexachloro-, beta-
Cyclohexane, 1,2,3,4,5,6-hexachloro-, trans-
1,2,3,4,5,6-hexachloro-cyclohexanbeta-isomer
1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE [B-ISOMER]
r-1,t-2,c-3,t-4,c-5,t-6-hexachlorocyclohexane
1,2,3,4,5,6-HEXACHLOROCYCLOHEXANE, BETA-ISOMER
Cyclohexane, 1,2,3,4,5,6-hexachloro-, beta-isomer
1-alpha,2-beta,3-alpha,4-beta,5-alpha,6-beta-Hexachlorocyclohexane
cyclohexane,1,2,3,4,5,6-hexachloro-,(1alpha,2beta,3alpha,4beta,5alpha,6
cyclohexane,1,2,3,4,5,6-hexachloro-,(1alpha,2beta,3alpha,4beta,5alpha,6b
(1alpha,2beta,3alpha,4beta,5alpha,6beta)-1,2,3,4,5,6-hexachlorocyclohexane
1,2,3,4,5,6-hexachloro-,(1.alpha.,2.beta.,3.alpha.,4.beta.,5.alpha.,6.beta.)-Cyclohexane
Cyclohexane, 1,2,3,4,5,6-hexachloro-, (1.alpha.,2.beta.,3.alpha.,4.beta.,5.alpha.,6.beta.)- | [EINECS(EC#)]
206-271-3 | [Molecular Formula]
C6H6Cl6 | [MDL Number]
MFCD00135948 | [MOL File]
319-85-7.mol | [Molecular Weight]
290.83 |
| Chemical Properties | Back Directory | [Appearance]
BHC is a white-to-brownish crystalline solid
with a musty, phosgene-like odor. | [Melting point ]
≥300 °C | [Boiling point ]
373.64°C (rough estimate) | [density ]
1.9 g/cm3 | [vapor pressure ]
4.66 at 25 °C (Banerjee et al., 1990) | [refractive index ]
1.630 (589.3 nm) | [Fp ]
11 °C | [storage temp. ]
APPROX 4°C
| [solubility ]
Soluble in ethanol, benzene, and chloroform (Weast, 1986) | [form ]
Solid | [Water Solubility ]
0.24mg/L(25 ºC) | [BRN ]
1907338 | [Henry's Law Constant]
0.53 at 5 °C, 0.91 at 10 °C, 2.17 at 20 °C, 5.23 at 30 °C, 8.68 at 35 °C:in 3% NaCl solution: 1.09
at 5 °C, 1.48 at 15 °C, 2.76 at 25 °C, 4.24 at 35 °C (dynamic headspace-GC, Sahsuvar et al.,
2003 | [EPA Substance Registry System]
.beta.-Hexachlorocyclohexane (319-85-7) |
| Hazard Information | Back Directory | [Uses]
β-1,2,3,4,5,6-Hexachlorocyclohexane is an organochloride which is one of the isomers of hexachlorocyclohexane and is also an byproduct of insecticide Lindane (L465990). | [Definition]
ChEBI: The beta-isomer of hexachlorocyclohexane. | [General Description]
Colorless crystals. Corrosive to aluminum and many other metals. | [Air & Water Reactions]
Slightly soluble in water. | [Reactivity Profile]
Halogenated aliphatic compounds, such as BETA-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. Dehydrochlorination occurs in the presence of alkalis. | [Health Hazard]
ACUTE/CHRONIC HAZARDS: Highly toxic carcinogen. May cause irritation on contact. Hazardous decomposition products. | [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 any
contact lenses at once and irrigate immediately for at least
30 minutes, occasionally lifting upper and lower lids. Seek
medical attention immediately. If this chemical contacts the
skin, remove contaminated clothing and wash immediately
with soap and water. Speed in removing material from skin
is of extreme importance. Shampoo hair promptly if con taminated. Seek medical attention immediately. If this
chemical has been inhaled, remove from exposure, begin
rescue breathing (using universal precautions, including
resuscitation mask) if breathing has stopped and CPR if
heart action has stopped. Transfer promptly to a medical
facility. When this chemical has been swallowed, get medi cal attention. Give large quantities of water and induce
vomiting. Do not make an unconscious person vomit. | [Shipping]
UN2761 Organochlorine pesticides, solid, toxic,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials. | [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. | [Chemical Properties]
BHC is a white-to-brownish crystalline solid
with a musty, phosgene-like odor. | [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. | [Physical properties]
Although β-BHC is a solid at room temperature, the odor threshold concentration is 0.32 μg/kg
(Sigworth, 1964). | [Environmental Fate]
Soil. No biodegradation of β-BHC was observed under denitrifying and sulfate-reduc ing conditions in a contaminated soil collected from The Netherlands (Bachmann et al.,
1988). In four successive 7-day incubation periods, β-BHC (5 and 10 mg/L) was recalci trant to degradation in a settled domestic wastewater inoculum (Tabak et al., 1981).
Chemical/Physical. Emits very toxic fumes of chlorides, hydrochloric acid and phos gene when heated to decomposition (Lewis, 1990). β-BHC will not hydrolyze to any
reasonable extent (Kollig, 1993). |
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BEST-REAGENT
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400-1166-196 18981987031 |
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| Company Name: |
Spectrum Chemical Manufacturing Corp.
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www.spectrumchemical.com/oa_html/index.jsp?minisite=10020&respid=22372&language=us |
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Grader reagent
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18221735425 |
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www.shxinping.net |
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