ChemicalBook > Product Catalog >Organic Chemistry >Hydrocarbons and derivatives >Cyclic hydrocarbons >CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B

CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B

CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B Structure
CAS No.
1024-57-3
Chemical Name:
CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B
Synonyms
HEPTACHLOROEPOXIDE;HCE;HEPTACHLOR-EXO-EPOXIDE;HEPTACHLOR-ENDO-EPOXIDE;beta-Heptachlorepoxide;TRANS-HEPTACHLOR EPOXIDE;TRANS-HEPTACHLOR-ENDO-EPOXIDE;Heptachlor-exo-epoxide (cis-, isomer B);Heptachlor epoxide (Isomer B) 50mg [1024-57-3];CAP1A
CBNumber:
CB6250742
Molecular Formula:
C10H5Cl7O
Molecular Weight:
389.32
MOL File:
1024-57-3.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:13

CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B Properties

Melting point 160-161.5℃
Boiling point 503.92°C (rough estimate)
Density 1.7335 (rough estimate)
vapor pressure 2.6(x 10-6 mmHg) at 20 °C (IARC, 1974)300(x 10-6 mmHg) at 30 °C (Nash, 1983)
refractive index 1.5000 (estimate)
Flash point 11 °C
storage temp. APPROX 4°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
color White to off-white
Water Solubility (μg/L):
350 at 25–29 °C (Park and Bruce, 1968)
275 at 25 °C (quoted, Warner et al., 1987)
Henry's Law Constant 0.59(x 10-5 atm?m3/mol) at 5 °C, 0.84 at 15 °C, 1.48 at 20 °C, 2.27 at 25 °C, 3.26 at 35 °C:in 3% NaCl solution: 2.07 at 5 °C, 4.93 at 15 °C, 7.70 at 25 °C, 9.28 at 35 °C (gas stripping-GC, Cetin et al., 2006)
Exposure limits ACGIH TLV: TWA 0.05 mg/m3 (adopted).
Stability Light Sensitive
EPA Substance Registry System Heptachlor epoxide (1024-57-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS08,GHS09
Signal word  Danger
Hazard statements  H300-H351-H373-H410
Precautionary statements  P202-P260-P264-P270-P273-P301+P310
Hazard Codes  T,N,F
Risk Statements  25-33-40-50/53-39/23/24/25-23/24/25-11-52/53
Safety Statements  36/37-45-60-61-16-7
RIDADR  2761
WGK Germany  3
RTECS  PB9450000
HazardClass  6.1(a)
PackingGroup  II
Toxicity Acute oral LD50 for rats 47 mg/kg (RTECS, 1985)

CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B Chemical Properties,Uses,Production

Uses

The cis-metabolite of organochlorine pesticide Heptachlor.

Definition

A degradation product of heptachlor that also acts as an insecticide.

General Description

Heptachlor epoxide is also a white powder. Bacteria and animals break down heptachlor to form heptachlor epoxide. The epoxide is more likely to be found in the environment than heptachlor. Heptachlor epoxide is a degradation product of heptachlor that occurs in soil and in or on crops when treatments with heptachlor, an insecticide, have been made. It forms readily upon exposing heptachlor to air. The U.S. EPA lists heptachlor epoxide as a possible human carcinogen.

Reactivity Profile

CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B may react with acids, bases, and oxidizing and reducing agents.

Hazard

Possible carcinogen.

Health Hazard

ACUTE/CHRONIC HAZARDS: Toxic.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.

Safety Profile

Confirmed carcinogen with experimental carcinogenic data. Poison by ingestion and intravenous routes. Human mutation data reported. When heated to decomposition it emits toxic fumes of Cl-. See also HEITACHLOR

Environmental Fate

Biological. In a model ecosystem containing plankton, Daphnia magna, mosquito larva (Culex pipiens quinquefasciatus), ?sh (Cambusia af?nis), alga (Oedogonium cardiacum) and snail (Physa sp.), heptachlor epoxide degraded to hydroxychlordene epoxide (Lu et al., 1975). Using settled domestic wastewater inoculum, heptachlor epoxide (5 and 10 mg/L) did not degrade after 28 days of incubation at 25°C (Tabak et al., 1981). This is consistent with the ?ndings of Bowman et al. (1965). They observed that under laboratory conditions, heptachlor epoxide did not show any evidence of degradation when incubated in a variety of soils maintained at 45°C for 8 days. The soils used in this experiment included Lakeland sand, Lynchburg loamy sand, Magnolia sandy loam, Magnolia sandy clay loam, Greenville sandy clay and Susquehanna sandy clay (Bowman et al., 1965). When heptachlor epoxide was incubated in a sandy loam soil at 28°C, however, 1hydroxychlordene formed at yields of 2.8, 5.8 and 12.0% after 4, 8 and 12 weeks, respectively (Miles et al., 1971).
Photolytic. Irradiation of heptachlor epoxide by a 450-W high-pressure mercury lamp gave two half-cage isomers, each containing a ketone functional group (Ivie et al., 1972). Benson et al. (1971) reported a degradation yield of 99% when an aceton
Graham et al. (1973) reported that when solid heptachlor epoxide was exposed to July sunshine for 23.2 days, 59.3% degradation was achieved. In powdered form, however, only 5 days were required for complete degradation to occur.
Chemical/Physical. Heptachlor epoxide will hydrolyze via nucleophilic attack at the epoxide moiety forming heptachlor diol which may undergo further hydrolysis forming heptachlor triol and hydrogen chloride (Kollig, 1993).

CIS-HEPTACHLOREPOXIDE EXO-, ISOMER B Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 115)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Inventichem +918790275459 Telangana, India 155 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Rasayan Trading Co. 08048606343 Ahmedabad, India 75 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20296 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21669 55 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29825 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-029-89586680 +86-18192503167 China 8930 58 Inquiry
1,4,5,6,7,8,8-heptachloro-2,3-epoxy-3a,4,7,7a-tetrahydro-7-methanoindan 2,3,4,5,6,7,7-heptachloro-1a,1b,5,5a,6,6a-hexahydro-2,5-methano-2h-indeno(1, 2,5-Methano-2H-indeno[1,2-b]oxirene, 2,3,4,5,6,7,7-heptachloro-1a,1b,5,5a,6,6a-hexahydro- 2,5-Methano-2H-indeno[1,2-b]oxirene, 2,3,4,5,6,7,7-heptachloro-1a,1b,5,5a,6,6a-hexahydro-, (1aalpha,1bbeta,2alpha,5alpha,5abeta,6beta,6aalpha)- 2,5-methano-2H-indeno[1,2-b]oxirene,2,3,4,5,6,7,7-heptachloro-1a,1b,5,5a,6,6a-hexahydro-,(1aα,1bβ,2α,5α,5aβ,6β,6aα)- 2,5-methano-2h-oxireno(a)indene,2,3,4,5,6,7,7-heptachlor-1a,1b,5,5a,6,6a-hexa 2,5-methano-2h-oxireno(a)indene,2,3,4,5,6,7,7-heptachloro-1a,1b,5,5a,6,6a-he 2-b)oxirene 2-b)oxirene,2,3,4,5,6,7,7-heptachloro-1a,1b,5,5a,6,6a-5-methano-2h-indeno(1 Heptachlor-exo CAP1A DKFZp686J2031 RNGTT C14327 Heptachlor-endo-epoxide (trans-) Heptachlor epoxide,HCE, Heptachlor exo-epoxide, exo-1,4,5,6,7,8,8-Heptachloro-2,3-epoxy-4,7-methano-3a,4,7,7a-tetrahydroindane, GPKh epoxide Heptepoxide 1,4,5,6,7,8,8-heptachloro-2,3-epoxy-3a,4 (1aR,1bS,2R,5S,5aR,6S,6aR)-rel-2,3,4,5,6,7,7-Heptachloro-1a,1b,5,5a,6,6a-hexahydro-2,5-Methano-2H-indeno[1,2-b]oxirene Heptachlor cis-Epoxide Heptachlor exo-epoxide Standard Heptachlor exo-epoxi (1aalpha,1bbeta,2alpha,5alpha,5abeta,6beta,6aalpha)-hexahydro 1,4,5,6,7,8,8-heptachloro-2,3-epoxy-2,3,3a,4,7,7a-hexahydro-4,7-methanoinden 1,4,5,6,7,8,8-heptachloro-2,3-epoxy-3a,4,7,7a-tetrahydro-4,7-methanoindane 4,7-methanoindan 4,7-Methanoindan, 1,4,5,6,7,8,8-heptachloro-2,3-epoxy-3a,4,7,7a-tetrahydro- 4,7-methanoindan,1,4,5,6,7,8,8-heptachloro-2,3-epoxy-3a,4,7,7i-tetrahydro- ENT 25,584 ent25,584 Epoxyheptachlor hepox heptachlorcis-oxide Heptachlore epoxide hydro- Velsicol 53-CS-17 velsicol53-cs-17 HCE, exo-1,4,5,6,7,8,8-Heptachloro-2,3-epoxy-4,7-methano-3a,4,7,7a-tetrahydroindane (-)-CIS-HEPTACHLOREPOXIDE (+)-CIS-HEPTACHLOREPOXIDE CIS-HEPTACHLOR-EXO-EPOXIDE (-)-CIS-HEPTACHLOROEPOXIDE (+)-CIS-HEPTACHLOROEPOXIDE HEPTACHLOR-ENDO-EPOXIDE (ISOMER A) HEPTACHLOREPOXID ISOMER A HEPTACHLOR-EXO-EPOXIDE ISOMER B xahydro- 1,4,5,6,7,8,8-HEPTACHLORO-2,3 EPOXY-4,7-ENDOMETHANO 3A,4,7,7A-TETRAHYDROINDENE (-)-TRANS-HEPTACHLOREPOXIDE (+)-TRANS-HEPTACHLOREPOXIDE TRANS-HEPTACHLOREPOXIDE ENDO-, ISOMER A HEPTACHLOR EPOXIDE ISOMER B, 1X1ML, MEOH , 20UG/ML HEPTACHLOR EXO-EPOXIDE ISOMER B, PESTANA HEPTACHLOR EPOXIDE ISOMER B 1X1ML MEOH 1 000UG/ML HEPTACHLOR EPOXIDE ISOMER A 1X1ML MEOH 1 000UG/ML HEPTACHLOR EPOXIDE, 50MG, NEAT IsomerB