- Melting point: :-35 °C (lit.)
- Boiling point: :83 °C (lit.)
- Density :1.256 g/mL at 25 °C (lit.)
- vapor density :3.4 (20 °C, vs air)
- vapor pressure :87 mm Hg ( 25 °C)
- refractive index :n
- Flash point: :60 °F
- storage temp. : 0-6°C
- solubility :7.9g/l
- form :Liquid
- color :APHA: ≤10
- Relative polarity :0.327
- Odor :Chloroform-like odor
- explosive limit :6.2-15.9%(V)
- Water Solubility :8.7 g/L (20 ºC)
- Merck :14,3797
- BRN :605264
- Henry's Law Constant :11.24 at 30 °C (headspace-GC, Sanz et al., 1997)
- Exposure limits :TLV-TWA 10 ppm (～40 mg/m3) (ACGIH), 1 ppm (NIOSH), 50 ppm (MSHA and OSHA); ceiling 2 ppm/15 min (NIOSH); carcinogenicity: Animal Sufficient Evidence, Human Limited Evidence (IARC).
- EPA Primary Drinking Water Standard :MCL:0.005,MCLG:zero
- FDA 21 CFR :173.230; 573.440; 172.710; 173.315; 175.105; 177.1580; 73.345; 73.615
- Substances Added to Food (formerly EAFUS) :ETHYLENE DICHLORIDE
- CAS DataBase Reference :107-06-2(CAS DataBase Reference)
- EWG's Food Scores :7-10
- FDA UNII :55163IJI47
- IARC :2B (Vol. 20, Sup 7, 71) 1999
- Proposition 65 List :Ethylene dichloride (1,2-Dichloroethane)
- NIST Chemistry Reference :Ethane, 1,2-dichloro-(107-06-2)
- EPA Substance Registry System :1,2-Dichloroethane (107-06-2)
- Hazard Codes :F,T
- Risk Statements :45-11-22-36/37/38-23/25-23
- Safety Statements :53-45-24-16-7
- RIDADR :UN 1184 3/PG 2
- WGK Germany :3
- RTECS :KI0525000
- F :3-10
- Autoignition Temperature :775 °F
- TSCA :Yes
- HS Code :2903 15 00
- HazardClass :3
- PackingGroup :II
- Hazardous Substances Data :107-06-2(Hazardous Substances Data)
- Toxicity :LD50 orally in rats: 770 mg/kg (Smyth)
3 2 0
- Signal wordDanger
- Hazard statements H350-H225-H301+H311+H331-H370-H302-H315-H319-H331-H335
- Precautionary statements P201-P280-P308+P313-P210-P260-P301+P310-P311-P303+P361+P353-P405-P501a-P370+P378-P403+P235-P261-P305+P351+P338
1,2-Dichloroethane Price More Price(53)
- Brand: Sigma-Aldrich
- Product number: 48613
- Product name : 1,2–Dichloroethane solution
- Purity: certified reference material, 200?μg/mL in methanol
- Packaging: 1 mL
- Price: $24.2
- Updated: 2021/03/22
- Buy: Buy
- Brand: Sigma-Aldrich
- Product number: 34872
- Product name : 1,2-Dichloroethane
- Purity: suitable for HPLC, ≥99.8%
- Packaging: 100 mL
- Price: $46.6
- Updated: 2021/03/22
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- Brand: Sigma-Aldrich
- Product number: 1.00955
- Product name : 1,2-Dichloroethane
- Purity: EMPLURA?
- Packaging: 1 L
- Price: $78.72
- Updated: 2021/03/22
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- Brand: Sigma-Aldrich
- Product number: 1601180
- Product name : Residual Solvent Class 1 - 1,2-Dichloroethane
- Packaging: 3x1.2ml
- Price: $109
- Updated: 2020/08/18
- Buy: Buy
- Brand: Sigma-Aldrich
- Product number: PHR2108
- Product name : 1,2-Dichloroethane
- Purity: Pharmaceutical Secondary Standard; Certified Reference Material
- Packaging: 3 x 1.2 mL
- Price: $109
- Updated: 2021/03/22
- Buy: Buy
1,2-Dichloroethane Chemical Properties,Usage,Production
1,2-Dichloroethane, also called ethylene dichloride (EDC), is a manufactured chemical that is not found naturally in the environment. It is used principally to synthesize vinyl chloride, which is further used to produce a variety of vinyl based plastics products, such as polyvinyl chloride (PVC) pipes, furniture, automobile upholstery, wall coverings, housewares, and automobile parts. It is used in solvents in closed systems for various extraction and cleaning purposes in organic synthesis. It is used as a leaded gasoline additive to remove lead, but with declining tendency. It is used as a dispersant in rubber and plastics, as a wetting and penetrating agent. It was used in ore flotation, as a metal degreaser, and in textile and PVC cleaning. It was also used as an insect fumigant for stored grains and in mushroom houses, a soil fumigant in peach and apple orchards. But due to its toxicity, it is no longer registered for use as an insect fumigant in the United States (IARC 1999).
- Chemical Properties 1,2-Dichloroethane is a clear and colorless, flammable liquid which has a pleasant, chloroform-like odor, and a sweetish taste. Decomposes slowly: turns dark and acidic on contact with air, moisture, and light. The Odor Threshold is 100 ppm.It is a volatile compound. It is relatively insoluble in water (8.6 × 103 mg/l at 25 °C) but soluble in various organic solvents and is miscible with alcohol, chloroform, and ether (NLM, 2013).
- Uses 1,2-dichloroethane is used in the synthesis of vinyl chloride and other organic compounds. It is also used as a solvent for nail lacquers, as a degreaser and metal cleaner, in adhesives, in pharmaceutical production, and in tobacco and spice extraction. Ethylene dichloride was historically used as an insecticide fumigant.
1,2-Dichloroethane is a clear, manufactured liquid that is not
found naturally in the environment. It evaporates quickly at
room temperature and has a pleasant smell and a sweet taste.
1,2-Dichloroethane burns with a smoky flame. The most
important use of 1,2-dichloroethane is to make vinyl chloride,
which is used to make a variety of plastic and vinyl products,
including polyvinyl chloride pipes and other important
construction materials, packaging materials, furniture and
automobile upholstery, wall coverings, housewares, and
automobile parts. 1,2-Dichloroethane is also used as a solvent
and is added to leaded gasoline to improve octane rating.
It is a central nervous system (CNS) depressant that produces symptoms ranging from nausea, vomiting, headache, lightheadedness, and weakness to stupor, disequilibrium, coma, and respiratory arrest. Typically, in severe cases, CNS signs appear first, followed by a quiescent period ultimately leading to oliguria and hepatic transaminasemia. These conditions may occasionally proceed to hepatorenal failure. Severe ingestions produce widespread organ injury (especially kidney, liver, and adrenal gland) as well as gastrointestinal bleeding.
- Chemical Properties Ethylene dichloride is one of the highest volume chemicals used in the United States. It is a colorless oily liquid with a chloroform-like odor, detectable over the range of 6–40 ppm,with a sweet taste. Ethylene dichloride (1,2-dichloroethane), which has a carbon-carbon single bond, should be distinguished from 1,2-dichloroethene, which has a carbon-carbon double bond. It is a skin irritant. Ethylene dichloride is also used as an extraction solvent, as a solvent for textile cleaning and metal degreasing, in certain adhesives, and as a component in fumigants for upholstery, carpets, and grain. Other miscellaneous applications include paint, varnish, and fi nish removers, soaps and scouring compounds, wetting and penetrating agents, organic synthesis, ore fl otation, and as a dispersant for nylon, rayon, styrene-butadiene rubber, and other plastics.
- Physical properties Clear, colorless, oily liquid with a pleasant, chloroform-like odor. The average least detectable odor threshold concentrations in water at 60 °C and in air at 40 °C were 12 and 52 mg/L, respectively (Alexander et al., 1982). Experimentally determined detection and recognition odor threshold concentrations were 25 mg/m3 (6 ppmv) and 165 mg/m3 (41 ppmv), respectively (Hellman and Small, 1974).
- Uses 1,2-Dichloroethane is used in the manufacture of acetyl cellulose and vinyl chloride; inpaint removers; as a fumigant; as a degreaser;as a wetting agent; and as a solvent for oils,waxes, gums, resins, and rubber.
Ethylene dichloride (1,2-dichloroethane), otherwise known as EDC, is produced by reacting chlorine or anhydrous hydrochloric acid with ethylene. The largest single use for EDC is the production of vinyl chloride monomer, which is used to produce poly vinyl chloride (PVC). EDC can also be used in the manufacture of other organic compounds, and as a solvent. Ethylene dichloride is a colorless, oily liquid with a chloroform-like smell. It has many uses in industry, with principal ones being the following:
As an intermediate in the manufacture of methyl chloroform, perchloroethylene, ethylene amines, polyvinyl chloride (PVC), sulfide compounds, vinyl chloride, and trichloroethane.
As an additive in gasoline (used as a lead scavenger), pharmaceutical products, color film, and pesticides.
As a solvent for rubber, tobacco extract, paint, printing inks, and varnish.
Miscellaneous uses include as an ingredient in fingernail polish, for metal degreasing, in extracting spices, and as a dry cleaning agent.
Two of the major uses for this chemical are the manufacture of PVC and as a lead scavenger in gasoline. The process for making EDC begins with crude oil or natural gas and sodium chloride. The hydrocarbon raw materials are converted to ethene (ethylene), and sodium chloride is electrolyzed to pruduce chlorine.
2 NaCl + 2 H2O = Cl2 + 2 NaOH + H2
This electrochemical process is also the major industrial route for sodium hydroxide production, so essentially the only side product from this initial reaction is hydrogen gas, which is later converted to water. Once the ethylene is produced from the crude hydrocarbons, it is reacted with chlorine gas:
C2H4 + Cl2 - C2H4Cl (1,2-dichloroethane)
Although its common name would lead one to believe otherwise, EDC does not contain a double bond. In one of its major industrial processes, the manufacture of PVC, the following reaction is carried out:
C2H4Cl = C2H3Cl (vinyl chloride) + HC1
The HC1 produced in this reaction is recycled to be used in the first reaction by oxidation of the hydrogen-chlorine bond.
EDC is a carcinogen and a mutagen. Assessments of 1,2-dichloroethane are in progress under the authority of the Clean Air Act, Safe Drinking Water Act (SDWA), Toxic Substances Control Act (TSCA), and the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). EDC is also listed under CERCLA as a hazardous material, and is required to be reported as such under Title III of SARA, otherwise known as the Community Right-to-Know Act.
- Uses manufacture of vinyl chloride, acetyl cellulose; solvent for fats, oils, waxes, gums, resins, and particularly for rubber. Has been used as insect and soil fumigant.
- Definition ChEBI: A member of the class of chloroethanes substituted by two chloro groups at positions 1 and 2.
- Production Methods In the United States, almost all ethylene dichloride produced at present is used as the starting material for preparation of vinyl chloride monomer. Other applications are much smaller.
- Production Methods Ethylene dichloride (EDC) is produced by reacting ethylene and chlorine in the presence of ferric chloride, using the liquid product as solvent. It is also produced by oxychlorination—ethylene, hydrogen chloride, and air are reacted at about 250 °C with a copper chloride catalyst.
A clear colorless liquid with a chloroform-like odor. Flash point 56°F. Denser than water and insoluble in water. Vapors are heavier than air. Density 10.4 lb / gal.
Ethylene dichloride was also used as an extraction solvent, as a solvent for textile cleaning and metal degreasing, in certain adhesives, and as a component in fumigants for upholstery, carpets, and grain. Other miscellaneous applications include paint, varnish, and finish removers, soaps and scouring compounds, wetting and penetrating agents, organic synthesis, ore flotation, and as a dispersant for nylon, rayon, styrene-butadiene rubber, and other plastics. Reports indicate that ethylene dichloride has extensive industrial and other applications around the globe.
- Air & Water Reactions Highly flammable. Slightly water soluble.
- Reactivity Profile Liquid ammonia and 1,2-Dichloroethane can cause an explosion when mixed, NFPA 491M, 1991. A tank of dimethyl amino propyl amine exploded violently when 1,2-Dichloroethane reacted with wet 1,2-Dichloroethane which had been the tank's previous contents [Doyle 1973]. Halogenated aliphatic compounds, such as 1,2-Dichloroethane , are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, epoxides, aluminum
- Hazard Toxic by ingestion, inhalation, and skin absorption; strong irritant to eyes and skin; a carcinogen. Flammable, dangerous fire risk, explosive limits in air 6–16%. Possible carcinogen.
The toxic symptoms from exposure to 1,2-dichloroethane include depression of the cen tral nervous system, irritation of the eyes,corneal opacity, nausea, vomiting, diarrhea,ulceration, somnolence, cyanosis, pulmonaryedema, and coma. Repeated exposure mayproduce injury to the kidney and liver. Inges tion of the liquid can cause death. A fataldose in humans may range between 30 and50 mL. The liquid is an irritant to the skinand damaging to the eyes.
LC50 value, inhalation (rats): 1000 ppm/7 hLD50 value, oral (rabbits): 860 mg/kg
1,2-Dichloroethane tested positive to thehistidine reversion–Ames test and othermutagenic tests. The compound is carcino genic to animals. Inhalation or oral adminis tration caused lung, gastrointestinal, and skincancers in mice and rats.
Flammable liquid; burns with a smoky flame;
flash point (closed cup) 13°C (56°F), (open
cup) 18°C (65°F); vapor pressure 62 torr at
20°C (68°F); the vapor is heavier than air and
can travel a considerable distance to a source
of ignition and flash back; autoignition tem perature 413°C (775°F); fire-extinguishing
agent: dry chemical, CO2, or foam; water
may be used to keep fire-exposed contain ers cool and to disperse the vapors and flush
away any spill.
1,2-Dichloroethane forms explosive mix tures with air, with LEL and UEL val ues of 6.2% and 16.0% by volume in air, respectively. Its reactions with alkali met als, powdered aluminum, or magnesium can be violent. It forms explosive mixtures with nitrogen tetroxide.
- Agricultural Uses Fumigant, Insecticide: Not approved for use in EU countries. Not registered for use in the U.S. When mixed with carbon tetrachloride, ethylene dichloride is used as a grain fumigant for bulk storage in bags, sealed containers, bins or on floors. In recent years, 1,2-dichloroethane has found wide use in the manufacture of ethylene glycol, diaminoethylene, polyvinyl chloride, nylon, viscose rayon, styrenebutadiene rubber, and various plastics. It is a solvent for resins, asphalt, bitumen, rubber, cellulose acetate, cellulose ester, and paint; a degreaser in the engineering, textile and petroleum industries; and an extracting agent for soybean oil and caffeine. It is also used as an antiknock agent in gasoline, a pickling agent and a dry-cleaning agent. It has found use in photography, xerography, water softening, and also in the production of adhesives, cosmetics, pharmaceuticals, and varnishes.
- Trade name BORER SOL®; BROCIDE®; DESTRUXOL BORER-SOL®; DOWFUME®[C]; DUTCH LIQUID®; DUTCH OIL®
- Safety Profile Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. An experimental transplacental carcinogen. A human poison by ingestion. Poison experimentally by intravenous and subcutaneous routes. Moderately toxic by inhalation, skin contact, and intraperitoneal routes. Human systemic effects by ingestion and inhalation: flaccid paralysis without anesthesia (usually neuromuscular blockage), somnolence, cough, jaundce, nausea or vomiting, hypermoulity, diarrhea, ulceration or bleeding from the stomach, fatty liver degeneration, change in cardiac rate, cyanosis, and coma. It may also cause dermatitis, edema of the lungs, toxic effects on the kidneys, and severe corneal effects. A strong narcotic. Experimental teratogenic and reproductive effects. A skin and severe eye irritant, and strong local irritant. Its smell and irritant effects warn of its presence at relatively safe concentrations. Human mutation data reported. if exposed to heat, flame, or oxidizers. Moderately explosive in the form of vapor when exposed to flame. Violent reaction with Al, N2O4, NH3, dimethylaminopropylamine. Can react vigorously with oxidzing materials and emit vinyl chloride and HCl. To fight fire, use water, foam, Co2, dry chemicals. When heated to decomposition it emits highly toxic fumes of Cland phosgene. See also CHLORINATED HYDROCARBONS, ALIPHATIC . Flammable liquid. A dangerous fire hazard
- Potential Exposure In recent years, 1,2-dichloroethane is used in the production of vinyl chloride and as a leadscavenging agent in petrol; it has found wide use in the manufacture of ethylene glycol, diaminoethylene, polyvinyl chloride; nylon, viscose rayon; styrenebutadiene rubber, and various plastics. It is a solvent for resins, asphalt, bitumen, rubber, cellulose acetate; cellulose ester; and paint; a degreaser in the engineering, textile, and petroleum industries; and an extracting agent for soybean oil and caffeine. It is also used as an antiknock agent in gasoline; a pickling agent; a fumigant; and a dry-cleaning agent. It has found use in photography, xerography, and water softening; and also in the production of adhesives, cosmetics, pharmaceuticals, and varnishes.
- Carcinogenicity 1,2-Dichloroethane is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.
- Source Improper use of insecticidal fumigant formulation containing 1,2-dichloropropane and carbon tetrachloride (Granosan).
Biological. Methanococcus thermolithotrophicus, Methanococcus deltae, and
Methanobacterium thermoautotrophicum metabolized 1,2-dichloroethane releasing methane and
ethylene (Belay and Daniels, 1987). 1,2-Dichloroethane showed slow to moderate biodegradative
activity with concomitant 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 63 and 53, respectively. At a substrate concentration of 5
mg/L, 27% was lost due to volatilization after 10 d (Tabak et al., 1981).
Photolytic. Titanium dioxide suspended in an aqueous solution and irradiated with UV light (λ = 365 nm) converted 1,2-dichloroethane to carbon dioxide at a significant rate (Matthews, 1986).
The rate constant for the reaction of 1,2-dichloroethane and OH radicals in the atmosphere at 300 K is 1.3 x 10-11 cm3/molecule?sec (Hendry and Kenley, 1979). At 296 K, a photooxidation rate constant of 2.2 x 10-13 cm3/molecule?sec was reported for the reaction with OH radicals resulting in a half-life of 1.7 months (Howard and Evenson, 1976).
Chemical/Physical. Anticipated products from the reaction of 1,2-dichloroethane with ozone or OH radicals in the atmosphere are chloroacetaldehyde, chloroacetyl chloride, formaldehyde, and ClHCHO (Cupitt, 1980).
- Metabolic pathway Resting cell suspensions of the soil methylotroph Methylosinus trichosporium OB-3b rapidly dehalogenate 1,2-dichloroethane, resulting in the formation of chloroethanol via direct hydroxylation of one of the C-Cl bonds, and this ethanol is rapidly oxidized to yield chloroacetic acid.
- storage Ethylene dichloride should be kept protected against physical damage. Store in a cool, dry, well-ventilated location, away from any area where the fi re hazard may be acute. Outside or detached storage is preferred. Separate from incompatibles. Containers should be bonded and grounded for transfer to avoid static sparks.
- Shipping UN1184 Ethylene dichloride, Hazard Class: 3; Labels: 3-Flammable liquid, 6.1-Poisonous materials. Note: United States DOT 49CFR172.101, Inhalation Hazardous Chemical as 1,2-Dichloroethane
- Purification Methods It is usually prepared by chlorinating ethylene, so that likely impurities include higher chloro derivatives and other chloro compounds depending on the impurities originally present in the ethylene. It forms azeotropes with water, MeOH, EtOH, trichloroethylene, CCl4 and isopropanol. Its azeotrope with water (containing 8.9% water, and b 77o) can be used to remove gross amounts of water prior to final drying. As a preliminary purification step, it can be steam distilled, and the lower layer is treated as below. Shake it with conc H2SO4 (to remove alcohol added as an oxidation inhibitor), wash with water, then dilute KOH or aqueous Na2CO3 and again with water. After an initial drying with CaCl2, MgSO4 or by distillation, it is refluxed with P2O5, CaSO4 or CaH2 and fractionally distilled. Carbonyl-containing impurities can be removed as described for chloroform. [Beilstein 1 IV 131.]
Ethylene dichloride (1) had been detected in surface and ground water as
an environmental contaminant, resulting from both industrial and
agricultural uses. It is also detected following the chlorination of drinking
water. Ethylene dichloride is stable to hydrolytic degradation at
environmentally relevant pH and temperature.
The primary dissipation mechanism of ethylene dichloride is volatilisation (DT50 30 min, Moore et al., 1991). Ethylene dichloride interacts with hydroxyl radicals produced by photo-oxidation in air to yield chloracetyl chloride (2, Howard and Evenson, 1976; Radding et al., 1977). The DT50 of ethylene dichloride in the vapour phase under atmospheric photo-oxidation conditions was 12-122 days (Atkinson, 1985).
1,2-Dichloroethane can enter the environment when it is made,
packaged, shipped, or used. Most 1,2-dichloroethane is released
to the air, although some is released to rivers or lakes.
1,2-Dichloroethane could also enter soil, water, or air in large
amounts in an accidental spill (evaporates into the air very fast
from soil and water). If released to air, a vapor pressure of
78.9mmHg at 25°Cindicates that 1,2-dichloroethane will exist
solely as a vapor in the ambient atmosphere. Vapor-phase
1,2-dichloroethane will be degraded in the atmosphere by
reaction with photochemically produced hydroxyl radicals; the
half-life for this reaction in air is estimated to be 63 days. Indirect
evidence for photooxidation of 1,2-dichloroethane comes
from the observation that monitoring levels are highest during
the night and early morning. It may also be removed from air
in rain or snow. Since it stays in the air for a while, the wind may
carry it over large distances. In water, 1,2-dichloroethane breaks
down very slowly and most of it will evaporate to the air. Only
very small amounts are taken up by plants and fish. Exact
longevity of 1,2-dichloroethane in water remains unknown.
It is thought that it remains longer in lakes than in rivers.
In soil, it either evaporates into the air or travels down through soil and enters underground water. 1,2-Dichloroethane has been found in the United States drinking water at levels ranging from 0.05 to 64 ppb. An average amount of 175 ppb has been found in 12%of the surface water and groundwater samples taken at 2783 hazardous wastes sites. 1,2-Dichloroethane has also been found in the air near urban areas at levels of 0.10–1.50 ppb and near hazardous waste sites at levels of 0.01–0.003 ppb. Small amounts of 1,2-dichloroethane have also been found in foods. Small organisms living in soil and groundwater may transform it into other, less harmful compounds, although this happens slowly. Large amounts from an accident, hazardous waste site, or landfill may likely reach the underground and contaminate drinking water wells. Biodegradation occurs slowly in water and soil surfaces. It is not expected to undergo hydrolysis and photolysis. Humans may get exposed to very lowlevels of 1,2-dichloroethane through its use as a gasoline additive (leaded gasoline is no longer used in the United States).
- Incompatibilities May form explosive mixture with air. Reacts violently with strong oxidizers and caustics; chemically active metals, such as magnesium or aluminum powder, sodium and potassium; alkali metals; alkali amides; liquid ammonia. Decomposes to vinyl chloride and HCl above 600℃. Attacks plastics, rubber, coatings. Attacks many metals in presence of water.
- 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
- Precautions Occupational workers should avoid use of ethylene dichloride along with oxidizing agents, strong alkalis, strong caustics, magnesium, sodium, potassium, active amines, ammonia List of Chemical Substances
1,2-Dichloroethane Preparation Products And Raw materials
- sulfonic ion exchange membrane based on polypropylene/poly (ST-DVB) TRIS(2-AMINOETHYL)AMINE 1-(5-BROMO-1-BENZOTHIEN-3-YL)ETHANONE 5-CHLORO-BENZO[B]THIOPHENE-3-CARBOXYLIC ACID 3-AMINO-4-METHOXYPYRIDINE Dazoxiben 5-(CHLOROMETHYL)-2-(TRIFLUOROMETHYL)THIAZOLE 1-ACETYLISONIPECOTOYL CHLORIDE (5-BROMO-3-BENZO[B]THIENYL)METHANOL PHENYL(PIPERIDIN-4-YL)METHANONE 2,6-DICHLORO-(2-CHLOROETHOXY)BENZENE 7-HYDROXYISOFLAVONE 1-(5-CHLOROBENZO[B]THIOPHEN-3-YL)ETHANONE 1-ACETYL-4-BENZOYLPIPERIDINE VINYL CHLORIDE 2-TRIFLUOROMETHYLQUINOLINE-7-CARBOXYLIC ACID 2-(2,6-Dichlorophenoxy)ethylhydrazine 1,2-Bis(diphenylphosphino)ethane nickel(II) chloride 4-Bromo-1-chloroisoquinoline NITROCYCLOHEXANE Paclobutrazol (5-CHLORO-1-BENZOTHIOPHEN-3-YL)METHANOL 5-BROMOBENZO[B]THIOPHENE-3-CARBOXYLIC ACID (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl Acephate dimethyl(2-phenoxyethyl)amine 1,5-Diazabicyclo[4.3.0]non-5-ene 1,1-DICHLOROETHANE CHLOROACETYL ISOCYANATE 1,1,2-Trichloroethane 3-AMINO-5-FLUOROPYRIDINE Triethylenetetramine 1-Boc-4-Methylaminopiperidine METHYL CYCLOHEXANEACETATE 3-(THIOPHEN-2-YL)ISOXAZOL-5-AMINE 6-O-Benzylguanine Pyrrole-2-carboxylic acid 3-Acetyl benz[b]thiophene 4-(2-(N-PHENYL-N-ETHYLAMINO)ETHOXY)-3,5-DICHLOROBENZENAMINE 1'-Acetonaphthone
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107-06-2, 1,2-Dichloroethane Related Search:
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- 1,2-DICHLOROETHANE, ABS., OVER MOLECULAR SIEVE (H2O <0.005%)
- 1 2-DICHLOROETHANE 99+% A.C.S. REAGEN&
- 1,2-DICHLOROETHANE EXTRA PURE
- 1,2-DICHLOROETHANE, 99.8%, HPLC GRADE
- 1,2 DICHLOROETHANE, 1X1ML, MEOH, 200UG/M L
- 1,2-DICHLOROETHANE, FOR HPLC
- 1,2-DICHLOROETHANE, ANHYDROUS, 99.8%
- 1 2-DICHLOROETHANE DIST. 5 L
- 1,2-DICHLOROETHANE OEKANAL
- 1 2-DICHLOROETHANE DIST. 1 L
- 1 2-DICHLOROETHANE ACS FOR &
- 1,2-DICHLOROETHANE, FOR LUMINESCENCE
- 1 2-DICHLOROETHANE CHROMASOLV PLUS F
- ACETONITRILE SPECTRANAL
- 1.2-DICHLOROETHANE GC STANDARD
- 1,2-Dichloroethane,99+%,for spectroscopy,laser grade
- 1,2-Dichloroethane,99+%,for spectroscopy
- 1,2-Dichloroethane,99.8%,Extra Dry
- 1,2-Dichloroethane,99.5%,for electronic use,residue free