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乙烯基氯

乙烯基氯用途

【用途一】
用作多种聚合物的共聚单体
【用途二】
塑料工业的重要原料,主要用于生产聚氯乙烯树脂。与醋酸乙烯、偏氯乙烯、丁二烯、丙烯腈、丙烯酸酯类及其他单体共聚生成共聚物,也可用作冷冻剂等。

乙烯基氯名称

[ CAS 号 ]:
75-01-4

[ 中文名 ]:
乙烯基氯

[ 英文名 ]:
Vinyl chloride

[中文别名 ]:

[英文别名 ]:

乙烯基氯物理化学性质

[ 密度 ]:
0.911 g/mL at 25 °C(lit.)

[ 沸点 ]:
-10 ºC

[ 熔点 ]:
-153.8 °C(lit.)

[ 分子式 ]:
C2H3Cl

[ 分子量 ]:
62.49820

[ 闪点 ]:
-56 ºC

[ 精确质量 ]:
61.99230

[ LogP ]:
1.36870

[ 外观性状 ]:
无色气体

[ 折射率 ]:
n20/D 1.3700(lit.)

[ 储存条件 ]:
库房通风低温干燥,轻装轻卸,与氧气、空气等助燃气体钢瓶分开存放

[ 水溶解性 ]:
acetone/carbon disulfide, MEK, THF: soluble

乙烯基氯MSDS

乙烯基氯毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
KU9625000
CHEMICAL NAME :
Ethylene, chloro-
CAS REGISTRY NUMBER :
75-01-4
BEILSTEIN REFERENCE NO. :
1731576
LAST UPDATED :
199806
DATA ITEMS CITED :
127
MOLECULAR FORMULA :
C2-H3-Cl
MOLECULAR WEIGHT :
62.50
WISWESSER LINE NOTATION :
G1U1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
DOWCC* Dow Chemical Company Reports. (Dow Chemical USA, Health and Environment Research, Toxicology Research Lab., Midland, MI 48640)
TYPE OF TEST :
LC50 - Lethal concentration, 50 percent kill
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
18 pph/15M
TOXIC EFFECTS :
Behavioral - tremor Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - respiratory depression
TYPE OF TEST :
LCLo - Lowest published lethal concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
20 pph/30M
TOXIC EFFECTS :
Behavioral - general anesthetic
TYPE OF TEST :
LCLo - Lowest published lethal concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
30 pph/30M
TOXIC EFFECTS :
Behavioral - general anesthetic
TYPE OF TEST :
LCLo - Lowest published lethal concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Mammal - species unspecified
DOSE/DURATION :
200 ppm/18M
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
23400 mg/kg/13W-I
TOXIC EFFECTS :
Liver - changes in liver weight Blood - other changes Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - transaminases
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
30 mg/m3/4H/26W-I
TOXIC EFFECTS :
Cardiac - arrhythmias (including changes in conduction) Cardiac - EKG changes not diagnostic of specified effects Cardiac - pulse rate
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
5000 ppm/7H/52W-I
TOXIC EFFECTS :
Liver - changes in liver weight Kidney, Ureter, Bladder - changes in bladder weight Endocrine - changes in spleen weight
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
400 mg/m3/24H/14W-C
TOXIC EFFECTS :
Behavioral - muscle contraction or spasticity Blood - changes in serum composition (e.g. TP, bilirubin, cholesterol) Liver - changes in liver weight
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
28000 ppm/7H/6W-I
TOXIC EFFECTS :
Nutritional and Gross Metabolic - weight loss or decreased weight gain Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - hepatic microsomal mixed oxidase (dealkylation, hydroxylation, etc.) Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - other transferases
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
2000 ppm/8H/92D-I
TOXIC EFFECTS :
Liver - changes in liver weight Endocrine - changes in spleen weight Blood - changes in leukocyte (WBC) count
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
9 gm/m3/4H/22W-I
TOXIC EFFECTS :
Cardiac - arrhythmias (including changes in conduction) Cardiac - EKG changes not diagnostic of specified effects Cardiac - pulse rate
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
30 mg/m3/26W-I
TOXIC EFFECTS :
Brain and Coverings - recordings from specific areas of CNS Blood - other changes Musculoskeletal - osteoporosis
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
200 ppm/14Y-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Liver - tumors
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
3463 mg/kg/52W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Liver - tumors Kidney, Ureter, Bladder - Kidney tumors
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1 ppm/4H/52W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Skin and Appendages - tumors
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
10000 ppm/4H female 12-18 day(s) after conception
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Reproductive - Tumorigenic effects - transplacental tumorigenesis Endocrine - tumors
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
21 mg/kg/65W-I
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Skin and Appendages - tumors Gastrointestinal - tumors
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
21 mg/kg/67W-I
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Skin and Appendages - tumors
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
50 ppm/30W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Vascular - tumors Skin and Appendages - tumors
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - hamster
DOSE/DURATION :
50 ppm/4H/30W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Blood - lymphoma, including Hodgkin's disease Skin and Appendages - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
50 ppm/7H/26W-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Vascular - tumors Skin and Appendages - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
100 ppm/7H/26W-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Liver - tumors Skin and Appendages - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
50 ppm/47W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Lungs, Thorax, or Respiration - tumors Liver - tumors
TYPE OF TEST :
TD - Toxic dose (other than lowest)
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
34 gm/kg/3Y-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Liver - angiosarcoma Kidney, Ureter, Bladder - Kidney tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
50 ppm/6H/4W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Lungs, Thorax, or Respiration - tumors Skin and Appendages - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
50 ppm/4H/30W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Liver - tumors Skin and Appendages - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
250 ppm/2Y-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Sense Organs and Special Senses (Ear) - effect, not otherwise specified Liver - angiosarcoma
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Human
DOSE/DURATION :
300 mg/m3/W-C
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Blood - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
5 ppm/4H/52W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Skin and Appendages - tumors
TYPE OF TEST :
TC - Toxic concentration (other than lowest)
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
50 ppm/6H/43W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Skin and Appendages - tumors
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
30 mg/m3
SEX/DURATION :
male 5 year(s) pre-mating
TOXIC EFFECTS :
Reproductive - Paternal Effects - spermatogenesis (incl. genetic material, sperm morphology, motility, and count)
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
100 ppm/6H
SEX/DURATION :
male 26 week(s) pre-mating
TOXIC EFFECTS :
Reproductive - Paternal Effects - testes, epididymis, sperm duct
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
500 ppm/7H
SEX/DURATION :
female 6-15 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus)
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
1500 ppm/24H
SEX/DURATION :
female 1-9 day(s) after conception
TOXIC EFFECTS :
Reproductive - Fertility - post-implantation mortality (e.g. dead and/or resorbed implants per total number of implants)
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
500 ppm/7H
SEX/DURATION :
female 6-15 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus) Reproductive - Specific Developmental Abnormalities - musculoskeletal system
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
250 ppm/6H
SEX/DURATION :
female 55 day(s) pre-mating
TOXIC EFFECTS :
Reproductive - Fertility - female fertility index (e.g. # females pregnant per # sperm positive females; # females pregnant per # females mated)
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
30000 ppm/6H
SEX/DURATION :
male 5 day(s) pre-mating
TOXIC EFFECTS :
Reproductive - Fertility - pre-implantation mortality (e.g. reduction in number of implants per female; total number of implants per corpora lutea)
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
500 ppm/7H
SEX/DURATION :
female 6-15 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus) Reproductive - Specific Developmental Abnormalities - musculoskeletal system
TYPE OF TEST :
TCLo - Lowest published toxic concentration
ROUTE OF EXPOSURE :
Inhalation
DOSE :
500 ppm/7H
SEX/DURATION :
female 6-18 day(s) after conception
TOXIC EFFECTS :
Reproductive - Fertility - litter size (e.g. # fetuses per litter; measured before birth) Reproductive - Specific Developmental Abnormalities - musculoskeletal system
TYPE OF TEST :
Sex chromosome loss and nondisjunction
TYPE OF TEST :
Morphological transformation
TYPE OF TEST :
DNA adduct
TYPE OF TEST :
DNA damage
TYPE OF TEST :
DNA inhibition
TYPE OF TEST :
Cytogenetic analysis
TYPE OF TEST :
Micronucleus test
TYPE OF TEST :
Cytogenetic analysis
TYPE OF TEST :
Cytogenetic analysis
TYPE OF TEST :
Sister chromatid exchange

MUTATION DATA

TYPE OF TEST :
Mutation in mammalian somatic cells
TEST SYSTEM :
Rodent - hamster Ovary
REFERENCE :
EVSRBT Environmental Science Research. (Plenum Pub. Corp., 233 Spring St., New York, NY 10013) V.1- 1972- Volume(issue)/page/year: 25,91,1982 *** REVIEWS *** ACGIH TLV-Confirmed human carcinogen DTLVS* The Threshold Limit Values (TLVs) and Biological Exposure Indices (BEIs) booklet issues by American Conference of Governmental Industrial Hygienists (ACGIH), Cincinnati, OH, 1996 Volume(issue)/page/year: TLV/BEI,1997 ACGIH TLV-TWA 13 mg/m3 (5 ppm) DTLVS* The Threshold Limit Values (TLVs) and Biological Exposure Indices (BEIs) booklet issues by American Conference of Governmental Industrial Hygienists (ACGIH), Cincinnati, OH, 1996 Volume(issue)/page/year: TLV/BEI,1997 IARC Cancer Review:Human Sufficient Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 19,377,1979 IARC Cancer Review:Animal Sufficient Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 19,377,1979 IARC Cancer Review:Group 1 IMSUDL IARC Monographs, Supplement. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) No.1- 1979- Volume(issue)/page/year: 7,373,1987 TOXICOLOGY REVIEW FAZMAE Fortschritte der Arzneimittelforschung. Progress in Drug Research. (Birkhauser Boston, Inc., c/o Springer-Verlag New York, 44 Hartz Way, Secaucus, NJ 07094) V.1- 1959- Volume(issue)/page/year: 18,365,1974 TOXICOLOGY REVIEW JTEHD6 Journal of Toxicology and Environmental Health. (Hemisphere Pub., 1025 Vermont Ave., NW, Washington, DC 20005) V.1- 1975/76- Volume(issue)/page/year: 1,47,1975 TOXICOLOGY REVIEW CMTVAS Cahiers de Medecine du Travail. (Association Professionnelle Belge des Medecine du Travail, rue du Bultia, 6280 Gerpinnes, Belgium) V.1- 1963- Volume(issue)/page/year: 10(3),49,1973 TOXICOLOGY REVIEW CHWEAP Chemisch-Weekblad. (The Hague, Netherlands) V.1-71, 1903-75. Volume(issue)/page/year: 70(28/29),5,1974 TOXICOLOGY REVIEW CANCAR Cancer (Philadelphia). (Lippincott/Harper, Journal Fulfillment Dept., 2350 Virginia Ave., Hagerstown, MD 21740) V.1- 1948- Volume(issue)/page/year: 39,1792,1977 TOXICOLOGY REVIEW MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 32,93,1975 TOXICOLOGY REVIEW ZHPMAT Zentralblatt fuer Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene, Abteilung 1: Originale, Reihe B: Hygiene, Krankenhaushygiene, Betriebshygiene, Praeventive Medizin. (Stuttgart, Fed. Rep. Ger.) V.155-169, 1971-1979. For publisher information, see ZAOMDC. Volume(issue)/page/year: 166,113,1978 TOXICOLOGY REVIEW BNYMAM Bulletin of the New York Academy of Medicine. (New York Academy of Medicine, 2 E. 103rd St., New York, NY 10029) Ser 2: V.1- 1925- Volume(issue)/page/year: 54,413,1978 TOXICOLOGY REVIEW ABMHAM Archives Belges de Medecine Sociale, Hygiene, Medecine du Trevail et Medecine Legale. (Quartier Esplanade no.6, 1010 Brussels, Belgium) V.4- 1946- Volume(issue)/page/year: 35,585,1977 TOXICOLOGY REVIEW CBINA8 Chemico-Biological Interactions. (Elsevier Scientific Pub. Ireland Ltd., POB 85, Limerick, Ireland) V.1- 1969- Volume(issue)/page/year: 22,117,1978 TOXICOLOGY REVIEW GTPZAB Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. (V/O Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.1-36, 1957-1992. For publisher information, see MTPEEI Volume(issue)/page/year: 20(4),46,1976 TOXICOLOGY REVIEW VHTODE Veterinary and Human Toxicology. (American College of Veterinary and Comparative Toxicology, Publication Office, Comparative Toxicology, Manhattan, KS 66506) V.19- 1977- Volume(issue)/page/year: 22,31,1980 TOXICOLOGY REVIEW MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 41,131,1976 *** U.S. STANDARDS AND REGULATIONS *** MSHA STANDARD-air:TWA 200 ppm (510 mg/m3) DTLWS* "Documentation of the Threshold Limit Values for Substances in Workroom Air," Supplements. For publisher information, see 85INA8. Volume(issue)/page/year: 3,31,1973 OSHA PEL (Construc):see CFR 29,1926.1117 CFRGBR Code of Federal Regulations. (U.S. Government Printing Office, Supt. of Documents, Washington, DC 20402) Volume(issue)/page/year: 29,1926.55,1994 OSHA PEL (Fed Cont):8H TWA 500 ppm (13 mg/m3) CFRGBR Code of Federal Regulations. (U.S. Government Printing Office, Supt. of Documents, Washington, DC 20402) Volume(issue)/page/year: 41,50-204.50,1994 OSHA-cancer suspect agent CFRGBR Code of Federal Regulations. (U.S. Government Printing Office, Supt. of Documents, Washington, DC 20402) Volume(issue)/page/year: 29,1910.1017,1987 *** OCCUPATIONAL EXPOSURE LIMITS *** OEL-ARAB Republic of Egypt:TWA 2.5 mg/m3 JAN 1993 OEL-AUSTRALIA:TWA 5 ppm (10 mg/m3);Carcinogen JAN 1993 OEL-BELGIUM:TWA 5 ppm (13 mg/m3);Carcinogen JAN 1993 OEL-DENMARK:TWA 1 ppm (3 mg/m3);Carcinogen JAN 1993 OEL-FINLAND:TWA 5 ppm (15 mg/m3);STEL 10 ppm (30 mg/m3);Carcinogen JAN 1993 OEL-FRANCE:TWA 1 ppm (3 mg/m3);Carcinogen JAN 1993 OEL-GERMANY;Carcinogen JAN 1993 OEL-HUNGARY:STEL 10 mg/m3;Carcinogen JAN 1993 OEL-JAPAN:STEL 2.5 ppm;Carcinogen JAN 1993 OEL-THE NETHERLANDS JAN 1993 OEL-THE PHILIPPINES:TWA 50 ppm (100 mg/m3) JAN 1993 OEL-POLAND:TWA 30 mg/m3 JAN 1993 OEL-RUSSIA:TWA 1 mg/m3;STEL 2.5 ppm (5 mg/m3) JAN 1993 OEL-SWEDEN:TWA 1 ppm (2.5 mg/m3);STEL 5 ppm (13 mg/m3);Skin;Carcinogen JAN 1993 OEL-SWITZERLAND:TWA 2 ppm (5.2 mg/m3);Carcinogen JAN 1993 OEL-THAILAND:TWA 1 ppm (2.8 mg/m3) JAN 1993 OEL-TURKEY:TWA 500 ppm (1300 mg/m3) JAN 1993 OEL-UNITED KINGDOM:TWA 7 mg/m3 JAN 1993 OEL IN BULGARIA, COLOMBIA, JORDAN, KOREA check ACGIH TLV OEL IN NEW ZEALAND, SINGAPORE, VIETNAM check ACGIH TLV *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH RECOMMENDED EXPOSURE LEVEL (REL) : NIOSH REL TO VINYL CHLORIDE-air:CA lowest feasible concentration REFERENCE : NIOSH* National Institute for Occupational Safety and Health, U.S. Dept. of Health, Education, and Welfare, Reports and Memoranda. Volume(issue)/page/year: DHHS #92-100,1992 NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 76445 No. of Facilities: 1459 (estimated) No. of Industries: 22 No. of Occupations: 36 No. of Employees: 29836 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - 76445 No. of Facilities: 3711 (estimated) No. of Industries: 63 No. of Occupations: 59 No. of Employees: 81314 (estimated) No. of Female Employees: 28398 (estimated)

乙烯基氯安全信息

[ 符号 ]:

GHS02, GHS06, GHS08

[ 信号词 ]:
Danger

[ 危害声明 ]:
H225-H301 + H311 + H331-H350-H370

[ 警示性声明 ]:
P201-P210-P260-P280-P301 + P310-P311

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
F+,T,F

[ 风险声明 (欧洲) ]:
R45

[ 安全声明 (欧洲) ]:
S53-S45-S36/37

[ 危险品运输编码 ]:
UN 1086 2.1

[ WGK德国 ]:
2

[ RTECS号 ]:
KU9625000

[ 危险类别 ]:
2.1

[ 海关编码 ]:
2903210000

乙烯基氯合成路线

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乙烯基氯制备

1、乙烯氧氯化法,乙烯与氯气在三氯化铁催化剂存在下,液相直接氯化生成1,2-二氯乙烷。1,2-二氯乙烷经精制后裂解,得氯乙烯和氯化氢,经精馏得到成品氯乙烯。副产氯化氢、乙烯与空气,通过载于氧化铝上的氯化铜触媒进行氧氯化反应得1,2-二氯乙烷,精制后在500℃、2.0-2.5MPa压力下,在管式炉内裂解生成氯乙烯和氯化氢,精制得产品氯乙烯。副产品氯化氢可再返回氧氯化反应器与乙烯再进行氧氯化反应 此法乙烯直接氯化转化率为99.7%,二氯乙烷选择为99%;二氯乙烷转化率为57%,氯乙烯选择性为99%。 每吨产品消耗定额:乙烯(100%计)485kg,氯气(100%)630kg,蒸汽(1.11MPa)1900kg,煤气90.15-0.20MPa)5.235×1000000KJ,电10000V±6%,50Hz±5%,8.64×100000KW/t。 2、乙烯直接氯化法 包括乙烯高温氯化和乙烯低温氯化等。
(1)乙烯低温氯化法 先向乙烯通氯,在三氯化铁存在下制取二氯乙烷,在碱的醇溶剂中,二氯乙烷再脱氯化氢制取氯乙烯,其反应如下:二氯乙烷裂解要在600℃以上进行。它除了脱第一个氯化氢生产氯乙烯外,还发生脱第二个氯化氢反应而生成乙炔,因而使氯乙烯产率降低。为了提高产率,必须使用催化剂,如活性炭、硅胶等,这样反应可以温度480-520℃下进行,氯乙烯产率可达85%。
(2)乙烯高温氯化法 以乙烯、氯气为原料,经高温氯化生产氯乙烯,同时副产多种氯代烃溶剂。整个工艺过程分热氯化、冷氯化和氧氯化三部分。其过程如下。
热氯化:乙烯、氯气和循环的二氯乙烷、三氯乙烷在热压反应釜内,于0.15MPa压力、374-495℃温度条件下反应,不用催化剂,生成氯乙烯经分离、精制而得产品,其佘二氯乙烷和三氯乙烷返回热压釜;氯化氢和未反应的乙烯送氧氯化工序。
冷氯化:使热氯化工序来的二氯乙烯与氯气反应成四氯乙烷,或与氯化氢反应得1,1,1-三氯乙烷,反应也不需要催化剂。所得四氯乙烷经热裂解而得三氯乙烯,氯化氢则送氧氯化工序。
氧氯化:以铜盐为催化剂,在0.2-0.78MPa、222-476℃温度下反应生成二氯乙烷、三氯乙烷、四氯乙烷和水,经分离得三氯乙烷、二氯乙烷产品,其佘氯代烃返回热氯化系统。
3、烯炔法 此法有两种。
(1)联合法 以乙烯、乙炔为原料,经氯化后,其中乙烯生成二氯乙烷;二氯乙烷裂解制氯乙烯,所副产的氯化氢与乙炔进行加成反应得氢乙烯,这样就可避免副产氯化氢。
该法采用的原料一半来自电石乙炔,一半来自石油乙烯。因此采用电石法生产氯乙烯的工厂,转向石油路线时,用此法作为过渡阶段比较简便,可以利用原有设备。
在国内采用重油为原料,经蓄热炉裂解,制成含乙烯25%-30%的混合气,再简易分离去除C3以上组分,制得的稀乙烯,与氯气在35-40℃、三氯化铁存在下,合成二氯乙烷。粗二氯乙烷经闪蒸精制,在管式炉内。其中副产氯化氢送往电石法氯乙烯工序合成氯乙烯。氯乙烯质量可达到聚合要求。
(2)混合烯炔法 以石脑油为原料,经2000℃的温度进行火焰裂解制得乙炔、乙烯混合气,在除去C3以上馏分和焦炭等杂质后,不经分离直接与氯化氢混合,在氯化汞催化剂存在下,乙炔与氯化氢反应生成氯乙烯,分离氯乙烯后的混合气体,通氯气与乙烯合成二氯乙烷;二氯乙烷再经热裂解得氯乙烯和氯化氢,氯化氢经提纯干燥后,送回,与混合气中的乙炔反应,用于合成氯乙烯。
裂解条件:炉温2000℃,常压,烯炔比1.2:1,烯烃产率48%-53%。氯乙烯产率:以乙炔计为95%-98%,以氯气计为99%,以乙烯计为95%-985;二氯乙烷转化率为50%,氯乙烯收率为96%。
4、电石乙炔法 以电石为原料制乙炔,在以活性炭为载体氯化汞催化剂存在下,与氯化加成而得。
配料摩尔比为:乙炔:氯化氢=1:(1.08-1.1)。乙炔和氯化氢按上述配比混合物后进行列管装有催化剂,借列管外的循环冷却水带走。反应气体中还含有未反应的氯化氢、乙炔和生成的乙醛、1,1-二氯乙烷及顺二氯乙烯、反二氯乙烯等化合物。反应后的粗氯乙烯气体,经水洗塔、碱洗塔,洗去气体中氯化氢及二氧化碳。碱洗后气体,通过干燥塔进行压缩全凝、液化,液体氯乙烯分别送入低沸点塔及高沸点塔,去除高、低沸点物即得聚合级氯乙烯单体。消耗定额(kg/t):乙炔429,氯化氢680,氯化汞2。

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乙烯基氯文献

Catalysis: The accelerator.

Nature 495(7440) , S10-1, (2013)

Biodegradable surfactant stabilized nanoscale zero-valent iron for in situ treatment of vinyl chloride and 1,2-dichloroethane.

J. Hazard. Mater. 211-212 , 373-80, (2012)

Nanoscale zero-valent iron (NZVI) stabilized with dispersants is a promising technology for the remediation of contaminated groundwater. In this study, we demonstrated the use of biodegradable surfact...

Considering pharmacokinetic and mechanistic information in cancer risk assessments for environmental contaminants: examples with vinyl chloride and trichloroethylene.

Chemosphere 31(1) , 2561-78, (1995)

Risk assessments for vinyl chloride (VC) and trichloroethylene (TCE) are presented as examples of approaches for incorporating chemical-specific pharmacokinetic and mechanistic information into a more...


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