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156-60-5

Basic Information
CAS No.: 156-60-5
Name: trans-1,2-Dichloroethylene
Article Data: 79
Molecular Structure:
Molecular Structure of 156-60-5 (trans-1,2-Dichloroethylene)
Formula: C2H2Cl2
Molecular Weight: 96.9439
Synonyms: Ethene,1,2-dichloro-, (E)-;Ethylene, 1,2-dichloro-, (E)- (8CI);Ethylene,1,2-dichloro-, trans- (5CI);(E)-1,2-Dichloroethene;(E)-1,2-Dichloroethylene;1,2-trans-Dichloroethene;Ethene, 1,2-dichloro-,(1E)-;HCC 1130t;NSC 60512;R1130t;trans-1,2-Dichloroethene;
EINECS: 205-860-2
Density: 1.243 g/cm3
Melting Point: ?57 °C(lit.)
Boiling Point: 47.7 °C at 760 mmHg
Flash Point: 6.1 °C
Solubility: Insoluble in water
Appearance: Clear liquid
Hazard Symbols: HarmfulXn, FlammableF, ToxicT
Risk Codes: 11-20-52/53-39/23/24/25-23/24/25
Safety: 7-16-29-61-45-36/37
Transport Information: UN 1150 3/PG 2
PSA: 0.00000
LogP: 1.93520
Synthetic route
79-00-5

1,1,2-trichloroethane

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
100%
50%
127-18-4

1,1,2,2-tetrachloroethylene

A

156-59-2

cis-1,2-Dichloroethylene

B

156-60-5

trans-1,2-dichloroethylene

C

79-01-6

Trichloroethylene

Conditions
ConditionsYield
With methanol at 20℃; Inert atmosphere; UV-irradiation;A n/a
B n/a
C 43%
With Desulfomonile tiedjei DCB-1 In water at 35℃; Kinetics; Further Variations:; Reagents; time; concentration; Dehalogenation;
156-59-2

cis-1,2-Dichloroethylene

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
at 100 - 250℃; Gleichgewicht der photochemischen Isomerisierung in der Gasphase im UV-Licht;
at 300℃; Gleichgewicht der thermischen Isomerisierung;
at 350℃; Gleichgewicht der thermischen Isomerisierung;
74-85-1

ethene

A

156-59-2

cis-1,2-Dichloroethylene

B

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
With oxygen; chlorine; copper(II) oxide at 375 - 425℃;
79-00-5

1,1,2-trichloroethane

A

156-59-2

cis-1,2-Dichloroethylene

B

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
With copper chloride +pumice stone at 400 - 450℃;
With copper chloride; pumice stone at 400 - 450℃;
79-00-5

1,1,2-trichloroethane

A

156-59-2

cis-1,2-Dichloroethylene

B

156-60-5

trans-1,2-dichloroethylene

C

75-35-4

1,1-Dichloroethylene

Conditions
ConditionsYield
at 500℃; bei der thermischen Zersetzung;
at 500℃; Geschwindigkeit dieser Spaltung bei verschiedenen Temperaturen und Beschleunigung der Pyrolyse durch geringe Mengen Sauerstoff oder Chlor;
74-86-2

acetylene

A

156-59-2

cis-1,2-Dichloroethylene

B

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
With chlorine In solid at -213.1℃; Product distribution; Quantum yield; Mechanism; Irradiation; various temperatures;
With antimonypentachloride
With nitrosylchloride at 350℃;
74-86-2

acetylene

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
With aqueous CuCl2+CuCl+NH4Cl at 50 - 85℃;
With iron(III) chloride; ammonium chloride; copper(l) chloride at 50 - 85℃;
With hydrogenchloride; water; copper(l) chloride at 80 - 110℃;
74-86-2

acetylene

A

156-60-5

trans-1,2-dichloroethylene

B

630-20-6

1,1,1,2-tetrachoroethane

Conditions
ConditionsYield
With chlorine; pyrographite at 40℃;
With chlorine; copper dichloride at 200 - 240℃;
79-34-5

1,1,2,2-tetrachloroethane

A

156-59-2

cis-1,2-Dichloroethylene

B

156-60-5

trans-1,2-dichloroethylene

Conditions
ConditionsYield
With sodium amalgam; water
With hydrogen; copper at 370 - 440℃;
With zinc In ethanol
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Chemistry

IUPAC Name: (E)-1,2-Dichloroethene 
Molecular Weight: 96.94328 g/mol
Molecular Formula: C2H2Cl2 
Density: 1.243 g/cm3 
Melting Point: −57 °C(lit.)
Boiling Point: 47.7 °C at 760 mmHg 
Flash Point: 6.1 °C
Index of Refraction: 1.453
Molar Refractivity: 21.07 cm3
Molar Volume: 77.9 cm3
Surface Tension: 25.9 dyne/cm 
Enthalpy of Vaporization: 27.93 kJ/mol
Vapour Pressure: 333 mmHg at 25 °C 
Exact Mass: 95.953355
EINECS: 205-860-2 
Properties: colourless liquid 
Product categories: Organics ; Analytical Chemistry ; Standard Solution of Volatile Organic Compounds for Water , Soil Analysis ; Standard Solutions (VOC) ; Alpha Sort ; D ; DAlphabetic ; DIA - DIC ; Volatiles/ Semivolatiles 
Mmolecular structure of  trans-1,2-Dichloroethylene (CAS NO.156-60-5):

Toxicity Data With Reference

1.    

skn-rbt 500 mg/24H MOD

    JACTDZ    Journal of the American College of Toxicology. 1 (1990),11.
2.    

eye-rbt 10 mg MOD

    JACTDZ    Journal of the American College of Toxicology. 1 (1990),11.
3.    

mma-smc 80 mmol/L

    TCMUD8    Teratogenesis, Carcinogenesis, and Mutagenesis. 4 (1984),365.
4.    

ihl-rat TCLo:12,000 ppm/6H (female 7-16D post):REP

    FAATDF    Fundamental and Applied Toxicology. 20 (1993),225.
5.    

ihl-hmn TCLo:4800 mg/m3/10M:CNS

    AHBAAM    Archiv fuer Hygiene und Bakteriologie. 116 (1936),131.
6.    

orl-rat LD50:1235 mg/kg

    TXCYAC    Toxicology. 7 (1977),141.
7.    

ipr-rat LD50:7411 mg/kg

    TXCYAC    Toxicology. 7 (1977),141.
8.    

orl-mus LD50:2122 mg/kg

    DCTODJ    Drug and Chemical Toxicology. 8 (1985),373.
9.    

ipr-rat LD50:7536 mg/kg

    TXCYAC    Toxicology. 7 (2)(1977),141.
10.    

ihl-mus LCLo:75,000 mg/m3/2H

    AHBAAM    Archiv fuer Hygiene und Bakteriologie. 116 (1936),131.
11.    

 

Consensus Reports

Reported in EPA TSCA Inventory.

Safety Profile

Moderately toxic by ingestion. Mildly toxic by inhalation. Human systemic effects by inhalation: sleep, hallucinations, and distorted perceptions. Experimental reproductive effects. A skin and eye irritant. Mutation data reported. Exposure to high vapor concentration can cause nausea, vomiting, weakness, tremor, and cramps. Recovery is usually prompt following removal from exposure. Dermatitis may result from defatting action on skin. Dangerous fire hazard when exposed to heat, flame, or oxidizers. Moderate explosion hazard in the form of vapor when exposed to flame. Violent reaction with difluoromethylene dihypofluorite. Forms shock-sensitive explosive mixtures with dinitrogen tetraoxide. Reaction with solid caustic alkalies or their concentrated solutions produces chloracetylene gas that ignites spontaneously in air. Reacts violently with N2O4, KOH, Na, NaOH. Moderate explosion hazard in the form of vapor when exposed to flame. Can react vigorously with oxidizing materials. To fight fire, use water spray, foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of Cl. See also CHLORIDES; CHLORINATED HYDROCARBONS, ALIPHATIC; and ACETYLENE COMPOUNDS and ALKYNES.
Hazard Codes: FlammableF, HarmfulXn, ToxicT
Risk Statements: 11-20-52/53-39/23/24/25-23/24/25 
R11: Highly flammable. 
R20: Harmful by inhalation. 
R52/53: Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
R39: Danger of very serious irreversible effects. 
R23/24/25: Toxic by inhalation, in contact with skin and if swallowed.
Safety Statements: 7-16-29-61-45-36/37 
S7: Keep container tightly closed. 
S16: Keep away from sources of ignition. 
S29: Do not empty into drains. 
S61: Avoid release to the environment. Refer to special instructions / safety data sheets. 
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) 
S36/37: Wear suitable protective clothing and gloves.
RIDADR: UN 1150 3/PG 2
WGK Germany: 2
RTECS: KV9400000
HazardClass: 3
PackingGroup: II

Standards and Recommendations

DFG MAK: 200 ppm (800 mg/m3)

Specification

The chemical synonyms of trans-1,2-Dichloroethylene (CAS NO.156-60-5) are (E)-1,2-Dichloroethene ; (E)-1,2-Dichloroethylene ; 4-01-00-00709 (Beilstein Handbook Reference) ; AI3-28786 ; BRN 1420761 ; CCRIS 2505 ; Ethylene, 1,2-dichloro-, trans- ; HCC 1130t ; HSDB 6361 ; NSC 60512 ; R 1130t ; RCRA waste number U079 ; trans-Acetylene dichloride ; trans-Dichloroethylene . It is highly flammable. Oxidizes in air to form unstable peroxides that may explode spontaneously. Avoid contact with copper and copper alloys. trans-1,2-Dichloroethylene reacts with alkalis, difluoromethylene, dihypofluorite, and nitrogen tetraoxide. Contact with solid alkalis or their concentrated solutions will cause formation of chloroacetylene, which ignites in air. Corrosive to metals unless an inhibitor has been added. Oxidation in the presence of concentrated sulfuric acid or a free radical initiator gives chloroacetyl chloride via epoxide intermediates. It is incompatible with organic peroxides.