trans-1,2-Dichloroethene
SmallMolecule
T3DB_ID
T3D0173
描述
Trans-1,2-dichloroethene (1,2-DCE) is one of two isomers of 1,2-dichloroethene. It is a highly flammable, colorless liquid with a sharp, harsh odor. 1,2-DCE is used as a solvent for waxes, resins, acetylcellulose, perfumes, dyes, lacquers, thermoplastics, fats, and phenols. It is also used as an intermediate in the preparation of other chlorinated solvents. (L585, L586)
类别
"Industrial/Workplace Toxin", "Pollutant", "Synthetic Toxin"
同义词
"(E)-1,2-Dichloroethene", "(E)-1,2-Dichloroethylene", "1,2-Dichloro Ethylene", "1,2-Dichloroethene", "1,2-Dichloroethylene", "1,2-Dichloroethylene (trans)", "1,2-trans-Dichloroethene", "1,2-trans-Dichloroethylene", "1,trans-2-Dichloroethene", "Acetylene dichloride", "cis or trans 1,2-Dichloroethene", "cis-1,2-Dichloroethylene", "Dichloroethylene-trans", "Dioform", "Ethene,1,2-dichloro", "SYM-dichloroethylene", "Trans-1, 2-Dichloroethene", "Trans-1,2-Dichloroethylene", "Trans-acetylene dichloride", "Trans-Di-1, 2-chloroethylene", "Trans-Di-1,2-Chloroethylene", "Trans-dichloroethene", "Trans-dichloroethylene"
CAS登记号
156-60-5
化学式
C2H2Cl2
平均分子量
96.943
单同位素质量
95.953355478
IUPAC 名称
(E)-1,2-dichloroethene
传统名称
trans-1,2-dichloroethylene
简化分子线性输入规范
Cl\C=C\Cl
InChI 标识符
InChI=1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1+
InChIKey=KFUSEUYYWQURPO-OWOJBTEDSA-N
化合物类型
Organic compounds
大分类
Organohalogen compounds
类型
Vinyl halides
子类
Vinyl chlorides
直接大类
Vinyl chlorides
另外分类
"Chloroalkenes", "Hydrocarbon derivatives", "Organochlorides"
取代基
"Aliphatic acyclic compound", "Chloroalkene", "Haloalkene", "Hydrocarbon derivative", "Organochloride", "Vinyl chloride"
分子框架
Aliphatic acyclic compounds
外部描述符
"1,2-dichloroethene"
地位
Detected and Not Quantified
起源
Exogenous
蜂窝位置
"Cytoplasm", "Extracellular"
生物流体位置
组织位置
途径
状态
Liquid
外貌
Colorless liquid.
熔点/沸点/溶解度
-49.8°C/47.2 °C at 745 mm Hg 48.0 - 48.5 °C at 760 mm Hg/6.41 mg/mL at 25 °C [HORVATH,AL et al. (1999)]
日志P
暴露途径
Inhalation (L585) ; oral (L585) ; dermal (L585) ; eye contact (L585)
毒性机制
Trans-1,2-dichloroethene is a volatile, lipophilic molecule that easily moves through the respiratory and gastrointestinal systems. It has a high affinity for lipids and blood, but little accumulation in tissues. 1,2-Dichloroethene isomers inhibit liver enzymes involved in metabolism and may increase the “toxic” response to other chemicals. Reactive metabolites of trans-1,2-dichloroethene modify the heme moiety of hepatic microsomal cytochrome P-450, resulting in a loss of both cytochrome P-450 and heme. Trans-1,2-dichloroethene can also mixed-function oxidase activities. Metabolism of trans-1,2-dichloroethene can lead to dose-related decrease in the levels of serum glutamicoxaloacetic transaminase (SGOT) and serum glutamic-pyruvic transaminase (SGPT). (L585)
代谢
Metabolism of trans-1,2-dichloroethene is initially catalyzed by hepatic microsomal cytochrome P-450. This metabolism is believed to involve epoxidation of the ethylene double bond, forming dichlorinated epoxides. Dichlorinated epoxides, in turn, can undergo a non-enzymatic rearrangement. Studies on the metabolism of 1,2-dichloroethene by hepatic microsomes and hepatocytes provide evidence to suggest that dichloroacetaldehyde is the predominant metabolite of microsomal cytochrome P-450 and that it, in turn, is extensively converted to dichloroethanol and dichloroacetate by cytosolic and/or mitochondrial aldehyde and alcohol dehydrogenases present in hepatocytes. (L585)
毒性值
LD50: 1 300-10 000 mg/kg/day (Inhalation, Rat) (L585)
致死剂量
致癌性
No indication of carcinogenicity (not listed by IARC). (L135)
用途/来源
Trans-1,2-DCE is used as a solvent for waxes, resins, acetylcellulose, perfumes, dyes, lacquers, thermoplastics, fats, and phenols. It is also used as an intermediate in the preparation of other chlorinated solvents. One may be exposed by breathing contaminated air, eating, or drinking the substance, or by skin contact (L585, L586).
最低风险等级
Acute Inhalation: 0.2 ppm (Rat) (L585) Acute Oral: 1 mg/kg/day (Rat) (L585) Intermediate Oral: 0.3 mg/kg/day (L585)
健康影响
Breathing trans-1,2-DCE can cause sever liver and kidney damages, pulmonary capillary hyperemia, as well as alveolar septal distention; depression of the central nervous sustem can occur; moderate iritis and conjunctivitis can follow eye exposure; dermatitis and irritation of mucous membranes can follow dermal exposure. Symptoms associated with lethal oral doses included decreased activity, ataxia, suppressed or total loss of righting reflex, and depressed respiration. (L585)
症状
Symptoms of trans-1,2-DCE exposure include nausea, dowiness, and tiredness. Mild or moderate erythema may follow dermal exposure, and skin or eye irritation can follow dermal/eye contact. (L585)
治疗
Following inhalation exposure, move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with inhaled beta2 agonist and oral or parenteral corticosteroids. In case of seizures, administer a benzodiazepine IV. Irrigate exposed eyes with copious amounts of room temperature water for at least 15 minutes in case of eye exposure. Following dermal exposure, remove contaminated clothing and wash exposed area thoroughly with soap and water. Treat dermal irritation or burns with standard topical therapy. Patients developing dermal hypersensitivity reactions may require treatment with systemic or topical corticosteroids or antihistamines. (T36)
药库 ID
HMDB_ID
PubChem 化合物 ID
638186
维基百科链接
创建于
2009-03-06 18:58:13 UTC
更新于
2014-12-24 20:21:16 UTC
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