trans-Dichlorethylen

TRANS-1,2-DICHLOROETHYLENE Struktur
156-60-5
CAS-Nr.
156-60-5
Bezeichnung:
trans-Dichlorethylen
Englisch Name:
TRANS-1,2-DICHLOROETHYLENE
Synonyma:
1,2-DICHLOROETHYLENE;TRANS-1,2-DICHLOROETHENE;tDCE;(E)-1,2-Dichloroethene;trans-dichloroethene;trans-Dichloroethylene;1,2-trans-Dichloroethene;(E)-1,2-Dichloroethylene;trans-1,2-Dichlorethylen;1,2-trans-Dichloroethylene
CBNumber:
CB7451926
Summenformel:
C2H2Cl2
Molgewicht:
96.94
MOL-Datei:
156-60-5.mol

trans-Dichlorethylen Eigenschaften

Schmelzpunkt:
−57 °C(lit.)
Siedepunkt:
48-60 °C(lit.)
Dichte
1.257 g/mL at 25 °C(lit.)
Dampfdruck
5.32 psi ( 20 °C)
Brechungsindex
n20/D 1.447(lit.)
Flammpunkt:
43 °F
storage temp. 
Refrigerator
Löslichkeit
Miscible with acetone, ethanol, and ether and very soluble in benzene and chloroform (U.S. EPA, 1985)
Aggregatzustand
Liquid
Farbe
Clear colorless
Explosionsgrenze
12.8%
Wasserlöslichkeit
Miscible with ethanol, ethyl ether, acetone, benzene and chloroform. Immiscible with water.
Merck 
14,92
BRN 
1420761
Henry's Law Constant
10.12 at 30 °C (headspace-GC, Sanz et al., 1997)
Expositionsgrenzwerte
OSHA PEL: TWA 200 ppm (790 mg/m3); ACGIH TLV: TWA 200 ppm (adopted).
Dielectric constant
2.27
Stabilität:
Incompatible with oxidizing agents, bases. Stable, but may decompose on exposure to air, moisture or light. Highly flammable.
LogP
2.06
CAS Datenbank
156-60-5(CAS DataBase Reference)
EPA chemische Informationen
trans-1,2-Dichloroethylene (156-60-5)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher F,Xn,T
R-Sätze: 11-20-52/53-39/23/24/25-23/24/25
S-Sätze: 7-16-29-61-45-36/37
RIDADR  UN 1150 3/PG 2
WGK Germany  2
RTECS-Nr. KV9400000
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29032990
Giftige Stoffe Daten 156-60-5(Hazardous Substances Data)
Toxizität LD50 in rats (ml/kg): 1.0 orally; 60 i.p.; in mice (ml/kg): 3.2 i.p. (Freundt)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H225 Flüssigkeit und Dampf leicht entzündbar. Entzündbare Flüssigkeiten Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS02.jpg" width="20" height="20" /> P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H332 Gesundheitsschädlich bei Einatmen. Akute Toxizität inhalativ Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P271, P304+P340, P312
H412 Schädlich für Wasserorganismen, mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 3 P273, P501
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P273 Freisetzung in die Umwelt vermeiden.

trans-Dichlorethylen Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R11:Leichtentzündlich.
R20:Gesundheitsschädlich beim Einatmen.
R52/53:Schädlich für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.

S-Sätze Betriebsanweisung:

S7:Behälter dicht geschlossen halten.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S29:Nicht in die Kanalisation gelangen lassen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.

Chemische Eigenschaften

colourless liquid

Physikalische Eigenschaften

Colorless, viscous liquid with a sweet, pleasant odor. Odor threshold concentration is 17 ppm (quoted, Amoore and Hautala, 1983).

Verwenden

trans-1,2-Dichloroethylene is used in the preparation of solvents and in chemical mixtures. It also acts as a synthetic agent and active constituent of perfumes. Further, it is used for electronics cleaning, precision cleaning and metal cleaning activities.

Allgemeine Beschreibung

Clear colorless liquid with a pleasant odor. Flash point 43°F.

Air & Water Reaktionen

Highly flammable. Oxidizes in air to form unstable peroxides that may explode spontaneously. Insoluble in water.

Reaktivität anzeigen

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. Avoid contact with copper and copper alloys. 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. Incompatible with organic peroxides .

Brandgefahr

TRANS-1,2-DICHLOROETHYLENE is flammable.

Sicherheitsprofil

Moderately toxic by ingestion. Mddly 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 oxidtzers. 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 alkahes 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.

mögliche Exposition

Primary irritant (w/o allergic reaction). 1,2-Dichloroethylene is used as a solvent for waxes, resins, and acetylcellulose. It is also used in the extraction of rubber, as a refrigerant; in the manufacture of pharmaceuticals and artificial pearls; and in the extraction of oils and fats from fish and meat.

Environmental Fate

Soil. In a methanogenic aquifer material, trans-1,2-dichloroethylene biodegraded to vinyl chloride (Wilson et al., 1986). Under anoxic conditions trans-1,2-dichloroethylene, when subjected to indigenous microbes in uncontaminated sediments, degraded to vinyl chloride (Barrio-Lage et al., 1986). trans-1,2-Dichloroethylene showed slow to moderate degradation concomitant with the rate of volatilization in a static-culture flask-screening test (settled domestic wastewater inoculum) conducted at 25 °C. At concentrations of 5 and 10 mg/L, percent losses after 4 wk of incubation were 95 and 93, respectively. The amount lost due to volatilization was 26 to 33% after 10 d (Tabak et al., 1981).
Biological. Heukelekian and Rand (1955) reported a 10-d BOD value of 0.05 g/g which is 7.6% of the ThOD value of 0.66 g/g.
Photolytic. Carbon monoxide, formic and hydrochloric acids were reported to be photooxidation products (Gay et al., 1976).

Versand/Shipping

UN1150 Dichloroethylene, Hazard Class: 3; Labels: 3-Flammable liquid.

läuterung methode

Dry it with MgSO4, and fractionally distil it under CO2. Fractional crystallisation at low temperatures has also been used. [Beilstein 1 IV 709.]

Inkompatibilitäten

May form explosive mixture with air. Attacks some plastics, rubber, and coatings. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, and epoxides. Gradual decomposition results in hydrochloric acid formation in the presence of ultraviolet light or upon contact with hot metal or other hot surfaces. Reacts with strong bases; potassium hydroxide; difluoromethylene, dihypofluoride, nitrogen tetroxide (explosive); or copper (and its alloys) producing toxic chloroacetylene which is spontaneously flammable on contact with air. Attacks some plastics and coatings.

Waste disposal

Incineration, preferably after mixing with another combustible fuel. Care must be exercised to assure complete combustion to prevent the formation of phosgene. An acid scrubber is necessary to remove the halo acids produced. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≧100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.

trans-Dichlorethylen Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


trans-Dichlorethylen Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 210)Lieferanten
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Dayang Chem (Hangzhou) Co.,Ltd.
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+8613288715578
sales@hbmojin.com China 12456 58
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sales@capotchem.com China 29797 60
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+86-0371-55170693 +86-19937530512
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008657128800458; +8615858145714
fandachem@gmail.com China 9348 55

156-60-5(trans-Dichlorethylen)Verwandte Suche:


  • 1,2-dichloroethylene,(transisomers)
  • 1,2-dichloroethylene,(E)-
  • 1,2-dichloro-ethylen
  • 1,2-dichloro-,(E)-Ethene
  • 1,2-Dichlorethentrans-
  • (E)-CHCl=CHCl
  • (E)-1,2-Dichlorethylen
  • (E)-1,2-Dichlorethen
  • trans-1,2-Dichloroethylene, 98%, stabilized
  • trans-1, 2-Dichloroethylene, 99.7%
  • trans-1,2-Dichloroethene in Dimethyl Sulfoxide, USP 467 Standard
  • TRANS-SYM-ACETYLENEDICHLORIDE
  • TRANS-1,2-DICHLOROETHYLENE
  • 2-dichloro-(e)-ethylen
  • Acetylene dichloride, trans-
  • Dichloroethylene, trans-
  • Ethene,1,2-dichloro-,(1E)-
  • Ethene,1,2-dichloro-,(E)-
  • ethene,1,2-dichloro-,trans-
  • Ethylene,1,2-dichloro-,(E)-
  • hcc1130t
  • r1130t
  • Rcra waste number U079
  • rcrawastenumberu079
  • trans-Acetylendichlorid
  • trans-Di-1,2-Chloroethylene
  • trans-Dichlorethen
  • trans-Dichlorethylen
  • trans-dichlorethylene
  • transdichloroethylene
  • TRANS-1,2-DICHLOROETHENE, 1X1ML, MEOH, 5 000UG/ML
  • TRANS-1,2-DICHLOROETHYLENE, STAB.
  • TRANS-1,2-DICHLOROETHENE, 5000MG, NEAT
  • TRANS-1,2-DICHLOROETHENE OEKANAL, AMYLENE STABILIZED, 1G
  • TRANS-1,2-DICHLOROETHENE, 1X1ML, MEOH, 2 00UG/ML
  • trans-1,2-Dichloroethylene, stabilized, 99.70%
  • trans-1,2-dichloroethene solution
  • Trans-1,2- twovinyl chloride
  • trans-1.2-Dich
  • trans-1,2-Dichloroethylene, stabilized with 4-methoxyphenol
  • 1,trans-2-Dichloroethene
  • 2-dichloro-(e)-ethen
  • trans-sym.-acethylenchlorid
  • TRANS-1,2-DICHLOROETHYLENE (STABILIZED WITH MEHQ)
  • trans-1,2-Dichloroethylene, 98%, stab. with 4-methoxyphenol
  • trans-1,2-Dichloroethylene (1mg/ml in Methanol) [for Water Analysis]
  • 1,2-DICHLOROETHANE extrapure AR
  • trans-1,2-Dichloroethene, trans-Acetylene dichloride
  • trans-1,2-Dichloroethene, trans-1,2-Dichloroethylene, trans-Acetylene dichloride
  • trans-1,2-Dichloroethylene 
  • trans-1,2-Dichloroethylene, 99+%, stabilized
  • trans-1,2-Dichloroethylene,trans-1,2-Dichloroethene, trans-Acetylene dichloride
  • trans-1.2-Dichloroethene 5g [156-60-5]
  • trans-1.2-Dichloroethene 2g [156-60-5]
  • trans-1,2-Dichloroethylene, stabilized, 99.7%
  • trans-1,2-Dichloroethylen
  • Trans-1,2-dichloroethylene, 99.70%, stabilized
  • trans-1,2-Dichloroethylene, stabilized
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