ChemicalBook > CAS DataBase List > 1,2-Dichloroethane

1,2-Dichloroethane

Product Name
1,2-Dichloroethane
CAS No.
107-06-2
Chemical Name
1,2-Dichloroethane
Synonyms
DCE;EDC;1,2-DCE;ETHYLENE DICHLORIDE;ETHYLENE CHLORIDE;CH2ClCH2Cl;1,2-Dichlorethane;1,2-Dichlorethan;Ethane,1,2-dichloro-;ethylene dichloride (eDC)
CBNumber
CB7295478
Molecular Formula
C2H4Cl2
Formula Weight
98.96
MOL File
107-06-2.mol
More
Less

1,2-Dichloroethane Property

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 
n20/D 1.444(lit.)
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)
Dielectric constant
10.7（20℃）
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).
Stability:
Volatile
LogP
1.45 at 20℃
CAS DataBase Reference
107-06-2(CAS DataBase Reference)
IARC
2B (Vol. 20, Sup 7, 71) 1999
NIST Chemistry Reference
Ethane, 1,2-dichloro-(107-06-2)
EPA Substance Registry System
1,2-Dichloroethane (107-06-2)
More
Less

Safety

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
OEB
B
OEL
TWA: 1 ppm (4 mg/m3), STEL: 2 ppm (8 mg/m3) (Chloroethanes)
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)
IDLA
50 ppm
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H350May cause cancer

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
PHR2108
Product name
1,2-Dichloroethane
Purity
Pharmaceutical Secondary Standard; Certified Reference Material
Packaging
3x1.2mL
Price
$145
Updated
2024/03/01
Sigma-Aldrich
Product number
DX0800
Product name
1,2-Dichloroethane
Purity
Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS
Packaging
4L
Price
$375
Updated
2024/03/01
Sigma-Aldrich
Product number
319929
Product name
1,2-Dichloroethane
Purity
ACS reagent, ≥99.0%
Packaging
18L
Price
$633
Updated
2024/03/01
Sigma-Aldrich
Product number
48613
Product name
1,2–Dichloroethane solution
Purity
certified reference material, 200?μg/mL in methanol
Packaging
1mL
Price
$31
Updated
2024/03/01
Sigma-Aldrich
Product number
284505
Product name
1,2-Dichloroethane
Purity
anhydrous, 99.8%
Packaging
1l
Price
$156
Updated
2024/03/01
More
Less

1,2-Dichloroethane Chemical Properties,Usage,Production

Description

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).

1,2-Dichloroethane structure

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). 1,2-Dichloroethane is one of the highest volume chemicals used in the United States. It 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.

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. It has been used as insect and soil fumigant.

Definition

ChEBI: 1,2-dichloroethane is a member of the class of chloroethanes substituted by two chloro groups at positions 1 and 2. It has a role as a non-polar solvent, a hepatotoxic agent and a mutagen.

Application

1,2-dichloroethane (Ethylene dichloride), also 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). 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.

Preparation

The first synthesis of 1,2-dichloroethane was achieved in 1795. 1,2-Dichloroethane is industrially produced by chlorination of ethylene. This chlorination can either be carried out by using chlorine (direct chlorination) or hydrogen chloride (oxychlorination) as a chlorinating agent. It is also produced by oxychlorination—ethylene, hydrogen chloride, and air are reacted at about 250 °C with a copper chloride catalyst. In the United States, almost all ethylene dichloride produced at present is used as the starting material for preparation of vinyl chloride monomer.

General Description

Ethylene Dichloride is a clear colorless liquid with a pleasant chloroform-like smell that emits toxic fumes of hydrochloric acid when heated to decomposition. Denser than water and insoluble in water. Vapors are heavier than air. Density 10.4 lb/gal. It is primarily used to produce vinyl chloride. Inhalation exposure to this substance induces respiratory distress, nausea and vomiting and affects the central nervous system, liver and kidneys. It is mutagenic in animals and is reasonably anticipated to be a human carcinogen. (NCI05)

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.

Health Hazard

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.

Fire Hazard

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.

Flammability and Explosibility

Highly flammable

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.

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.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Medical observation is recommended for 24- 48 h afterbreathing overexposure, as pulmonary edema may bedelayed. As first aid for pulmonary edema, a doctor orauthorized paramedic may consider administering a corticosteroid spray.

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).

Environmental Fate

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.]

Degradation

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).

Toxicity evaluation

The estimated daily intake of 1,2-dichloroethane was similar for each rat strain at each dose level. Rats administered drinking water containing 8,000 ppm 1,2-dichloroethane received an esti mated intake of about 500-725 mg/kg per day. This estimated daily intake is close to the report ed oral LDso for 1,2-dichloroethane adminis tered by gavage (680-850 mg/kg) (McCollister et al., 1956); however, intake of this dose over 24 hours rather than as a bolus resulted in little toxicity.
1,2-Dichloroethane toxicity administered by gavage or in formulated drinking water was compared in F344/N rats. Gavage doses were calculated to be approximately equivalent (in milligrams per kilogram) to the range of expo sures resulting from the formulated water mix tures. The F344/N rats were more sensitive to 1,2-dichloroethane administered by gavage than in drinking water, as evidenced by the fact that all males receiving 240 and 480 mg/kg and 9/10 females receiving 300 mg/kg died before the end of the studies.
Toxic encephalopathy is the most common and serious disorder resulting from DCE intoxication.

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

References

https://www.atsdr.cdc.gov/substances/toxsubstance.asp?toxid=110
[2] http://apps.who.int/iris/bitstream/10665/42027/1/9241530014.pdf
[3] https://www.epa.gov/sites/production/files/2016-09/documents/ethylene-dichloride.pdf

1,2-Dichloroethane Preparation Products And Raw materials

Raw materials

Chloral Ethylene Ethanol ETHYLENE OXIDE Chlorine 2-Chloroethanol Metal catalyst Phosphorus trichloride Petroleum cracking gas Hydrochloric acid Aluminum oxide

Preparation Products

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
More
Less

1,2-Dichloroethane Suppliers

Belgium 2 Canada 2 China 314 Czech Republic 1 Europe 2 France 3 Germany 10 India 49 Japan 6 Norway 1 Slovakia 1 South Korea 1 Switzerland 1 The Netherlands 1 Ukraine 1 United Kingdom 12 United States 64 Global 471
Huai 'an dongyu chemical co. LTD
Tel
0517-85399628 13770478962
Country
China
ProdList
1
Advantage
58
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Yikang Chemical（Hubei）Co.， LTD
Tel
027-18971353-902 18971353902
Email
2242508613@qq.com
Country
China
ProdList
7871
Advantage
58
Shandong Jinyueyuan New Material Co. Ltd
Tel
18615187817
Email
2793152786@qq.com
Country
China
ProdList
393
Advantage
58
jinan Liyang Chemical Co., Ltd
Tel
0531-0531-82370399 18765887256
Email
995071992@qq.com
Country
China
ProdList
87
Advantage
58
Jinan Trands Chemical Co. LTD
Tel
0531-88770911 15154153272
Fax
0531-88770911
Email
1343989492@qq.com
Country
China
ProdList
111
Advantage
58
Shandong Mantang Hongxin Material Co. , Ltd.
Tel
13065055261
Email
1643589804@qq.com
Country
China
ProdList
210
Advantage
58
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20806
Advantage
60
Shandong Xinyida Chemical Technology Co., Ltd
Tel
15806621738
Email
15806621738@163.com
Country
China
ProdList
123
Advantage
58
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Fax
010-60270825
Email
elainezt@sina.com
Country
China
ProdList
1390
Advantage
62
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12438
Advantage
60
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9414
Advantage
66
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14103
Advantage
59
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
Country
China
ProdList
19173
Advantage
64
Chemsky（shanghai）International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18738
Advantage
57
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
China Langchem Inc.
Tel
0086-21-58956006
Fax
0086-21-58956100
Country
China
ProdList
7811
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11707
Advantage
57
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9658
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9718
Advantage
55
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9865
Advantage
52
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22514
Advantage
55
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9545
Advantage
55
Cantotech Chemicals, Ltd.
Tel
86-0755-86635001
Fax
86-0755-22642228
Email
cantotech@126.com
Country
China
ProdList
4566
Advantage
55
Shanghai BeiZhuo Biotech Co., Ltd.
Tel
021-61119791,13386096464
Fax
021-50190009
Email
bzswkf@foxmail.com
Country
China
ProdList
3921
Advantage
50
Beijing Universal Century Technology Co., Ltd.
Tel
400-8706899
Fax
400-8706899
Email
hysj_bj.com
Country
China
ProdList
3583
Advantage
55
Shanghai Meishui Chemical Technology Co., Ltd
Tel
021-60549325 18616193163
Fax
021-33250306
Country
China
ProdList
4526
Advantage
56
RiZhao LiDeShi Chemical Co., Ltd.
Tel
010-51268198
Fax
010-63833209
Email
leadershipchem@126.com
Country
China
ProdList
2546
Advantage
58
Shanghai ideal Industrial Co., Ltd.
Tel
021-58957966 18930537195
Fax
021-60899437
Email
wouchina@126.com
Country
China
ProdList
3027
Advantage
58
HUBEI RISON CHEMICAL CO.,LTD
Tel
027 83642615 13995607107
Fax
027 83660699
Email
market@risonchem.com
Country
China
ProdList
279
Advantage
58
GuangTuo Chemical (Shanghai) Co., Ltd.
Tel
021-60899189-8001 18918189673
Fax
021-60899304
Email
gtchem@126.com
Country
China
ProdList
2656
Advantage
58
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15178
Advantage
58
Shanghai Heng Yue Chemical Technology Co., Ltd.
Tel
51691706 13391095697
Fax
+86-021-58619266
Email
info@hyscientific.com
Country
China
ProdList
159
Advantage
56
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
16166
Advantage
55
SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.
Tel
021-69106960 13701823733
Fax
021-69106780
Email
13701823733@163.com
Country
China
ProdList
4767
Advantage
60
Shanghai YouPeng Chemical Co. Ltd.
Tel
021-69005955 13701776567
Fax
021-69005775
Email
youpengchem@163.com
Country
China
ProdList
4293
Advantage
56
Shanghai TongYuan Chemical Co., Ltd.
Tel
021-021-69182866 13701855675
Fax
021-69182022
Email
tongyuanchem@126.com
Country
China
ProdList
4321
Advantage
58
Shanghai Kaisai Chemical Co., Ltd
Tel
021-33516722 13701817765
Fax
021-33516776
Email
kaisaichem@163.com
Country
China
ProdList
4741
Advantage
58
Chengdu RunZeBenTu Chemical Co., Ltd
Tel
13096311329 028-88469284 616445927
Fax
028-88469284
Email
616445927@qq.com
Country
China
ProdList
2874
Advantage
50
Shanghai LanRun Chemical Co., Ltd.
Tel
021-69515658 ; 69515628 13701998368
Fax
021-69515998
Email
longrunchem@163.com
Country
China
ProdList
3912
Advantage
50
Shanghai Rolead Chemical Technology Co., Ltd.
Tel
021-69992220 13701886816
Fax
021-69992237
Email
roleadchem@163.com
Country
China
ProdList
4750
Advantage
50
Shanghai Kangtuo Chemical Co., Ltd.
Tel
021-69185552 13701777608
Fax
021-69186006
Email
kangtuochem@163.com
Country
China
ProdList
4360
Advantage
55
More
Less

View Lastest Price from 1,2-Dichloroethane manufacturers

Qingdao RENAS Polymer Material Co., Ltd.
Product
1,2-Dichloroethane 107-06-2
Price
US $0.00/kg
Min. Order
20kg
Purity
99.0%
Supply Ability
20 tons
Release date
2024-06-25
Hebei Weibang Biotechnology Co., Ltd
Product
1,2-Dichloroethane 107-06-2
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100 mt
Release date
2021-08-17
Henan Fengda Chemical Co., Ltd
Product
1,2-Dichloroethane 107-06-2
Price
US $100.00-1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2023-12-26

107-06-2, 1,2-Dichloroethane Related Search:

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride ETHYLENE POLYETHYLENE, CHLORINATED Sodium chloride Cobalt chloride ETHYLENE OXIDE Ethylene glycol Polyethylene Ethambutol dihydrochloride Ethambutol Related Compound A (15 mg) ((2R,2'S)-2,2'-[ethane-1,2-diylbis(azanediyl)]dibutan-1-ol) 2-AMINO-1-BUTANOL l-Ethambutol (R)-(-)-2-Amino-1-butanol 1,1-Dichloroethane 1,1-DIFLUOROTETRACHLOROETHANE 1,1,1,2-TETRACHLOROETHANE Chloroacetyl chloride 1,2-DICHLOROTETRAFLUOROETHANE Ethylene Dichloride

  • 1,2-Bichloroethane
  • 1,2-DCE
  • 1,2-Dichloorethaan
  • 1,2-Dichlor-aethan
  • 1,2-Dichlorethan
  • 1,2-Dichlorethane
  • 1,2-dichloro-ethan
  • 1,2-dichloroethane (ethylene dichloride)
  • 1,2-dichloroethane,anhydrous
  • 1,2-Dichlorαthan
  • 1,2-Dichlorαthan(Hochtemperaturform)
  • 1,2-Dicloroetano
  • 1,2-Ethylene dichloride
  • 1,2-DICHLOROETHANE, 99.5%, RESIDUE FREE, FOR ELECTRONIC USE
  • 1,2-Dichloroethane, pure
  • 1,2-Dichloroethane, 99+%, laser grade, for spectroscopy
  • 1,2-Dichloroethane, 99+%, for analysis ACS
  • 1,2-Dichloroethane, for spectroscopy
  • 1,2-Dichloroethane, AcroSeal, Extra Dry
  • 1,2-Dichloroethane, residue free, for electronic use
  • 1,2-Dichloroethane, laser grade, for spectroscopy
  • 1,2-Dichloroethane, for analysis ACS
  • 1,2-Dichloroethane, ACS reagent, for spectroscopy
  • 1,2-Dichloroethane (1mg/ml in Methanol) [for Water Analysis]
  • 1,2-Dichloroethane [for HPLC Solvent]
  • Glycol dicholride
  • ethylene dichloride (eDC)
  • 1,2-DICHLOROETHANE ACS REAGENT
  • 1,2-DICHLOROETHANE, FOR PROTEIN SEQUENCE ANALYSIS
  • 1,2-DICHLOROETHANE, REAGENTPLUS, 99%
  • 1,2-DICHLOROETHANE, 500MG,NEAT
  • 1,2-DICHLOROETHANE, STANDARD FOR GC
  • 1,2-DICHLOROETHANE, 99+%, SPECTROPHOTO-M ETRIC GRADE
  • 1,2-DICHLOROETHANE, 99+%, A.C.S. REAGENT
  • 1,2-DICHLOROETHANE, ACS
  • 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
  • N-Decane,Certified
  • 1,2-Dichloroethane(EthyleneChloride)
  • 1,2-Dichloroethane,Certified
  • 1,2-DichloroethaneGr(EthyleneChloride)
  • 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