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ethylene glycol, chlorohydrin

ethylene chlorohydrin

CAS: 107-07-3

Molecular Formula: C2H5ClO

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ethylene glycol, chlorohydrin - Names and Identifiers

Name ethylene chlorohydrin
Synonyms Chloroethanol
2-chloro-ethano
2-Chloorethanol
2-Chloraethanol
2-chloroethanol
2-Chloro-1-ethanol
delta-chloroethanol
Glycol chlorohydrin
2-monochloroethanol
2-chloroethylalcohol
ethylene chlorohydrin
glycomonochlorohydrin
2-Chloroethyl alcohol
glycol monochlorohydrin
beta-chloroethyl alcohol
2-Chloro-1-hydroxyethane
1-Chloro-2-hydroxyethane
ethylene glycol, chlorohydrin
CAS 107-07-3
EINECS 203-459-7
InChI InChI=1/C2H5ClO/c3-1-2-4/h4H,1-2H2

ethylene glycol, chlorohydrin - Physico-chemical Properties

Molecular FormulaC2H5ClO
Molar Mass80.51
Density1.201g/mLat 25°C(lit.)
Melting Point-63 °C
Boling Point129°C(lit.)
Flash Point140°F
Water SolubilityMISCIBLE
Solubility Soluble in alcohol (Weast, 1986)
Vapor Presure5 mm Hg ( 20 °C)
Vapor Density2.78 (vs air)
AppearanceLiquid
ColorYellow
OdorFaint, ethereal.
Exposure LimitCeiling limit 3 mg/m3 (1 ppm) skin(ACGIH); TLV-TWA air 16 mg/m3 (5 ppm)skin (OSHA); IDLH 10 ppm (NIOSH).
Merck14,3793
BRN878139
pKa14.02±0.10(Predicted)
Storage Condition2-8°C
StabilityStable. Incompatible with oxidizing agents.
SensitiveMoisture Sensitive
Refractive Indexn20/D 1.441(lit.)
Physical and Chemical PropertiesCharacter: colorless transparent liquid.
melting point -62.6 ℃
boiling point 128.7 ℃
relative density 1.2045
refractive index 1.4417
flash point 57.2 ℃
solubility, ethanol can be mixed in any proportion.
UseUsed in the manufacture of ethylene oxide, synthetic rubber, dyes, pharmaceuticals and pesticides, is also an organic solvent

ethylene glycol, chlorohydrin - Risk and Safety

Risk CodesR26/27/28 - Very toxic by inhalation, in contact with skin and if swallowed.
R39/23/24/25 -
R23/24/25 - Toxic by inhalation, in contact with skin and if swallowed.
R11 - Highly Flammable
R10 - Flammable
Safety DescriptionS28 - After contact with skin, wash immediately with plenty of soap-suds.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S7/9 -
S28A -
S36/37 - Wear suitable protective clothing and gloves.
S16 - Keep away from sources of ignition.
S7 - Keep container tightly closed.
UN IDsUN 1135 6.1/PG 1
WGK Germany3
RTECSKK0875000
FLUKA BRAND F CODES21
TSCAYes
HS Code29333999
Hazard Class6.1
Packing GroupI
ToxicityLD50 orally in rats: 0.095 g/kg (Smyth)

ethylene glycol, chlorohydrin - Upstream Downstream Industry

Raw MaterialsEthylene Oxide
Hydrochloric acid
Downstream Products1-Bromo-2-fluoroethane
Choline chloride
trihydroxyethylrutin
diphenhydramine

ethylene glycol, chlorohydrin - Nature

Open Data Verified Data

colorless transparent liquid, toxic! The relative density (d20) was 1. 2045. Boiling point 128.7 °c. Melting Point -62.6 °c. Refractive index 4417. Flash point (closed cup) 57.2 °c. Viscosity (20 deg C) 3.42mPa.s. The surface tension was 38.9 RNNM. With water, ethanol can be mixed in any proportion.

Last Update:2024-01-02 23:10:35

ethylene glycol, chlorohydrin - Preparation Method

Open Data Verified Data
  1. The chlorohydrin method uses alcohol as a raw material to catalyze dehydration of aluminum oxide to generate ethylene, which is introduced into water at the same time as chlorine, and chlorine reacts with water to generate hypochlorous acid, which is added with ethylene to obtain dilute chloroethanol, after neutralization and distillation, the final product was obtained.
  2. The hydrochloric acid method is obtained by reacting hydrochloric acid and ethylene oxide with heating.
Last Update:2022-01-01 10:15:36

ethylene glycol, chlorohydrin - Safety

Open Data Verified Data
  • toxic, in the body tissue hydrolysis to produce hydrogen chloride. Inhalation of high concentrations of chlorine ethanol vapor or skin contact and absorption, can cause Vomit, Head Pain, tremor, body temperature, limb paralysis, heart pain and death. In most cases, a critical condition occurs several hours after poisoning. When severe, the patient presented with severe symptoms Head Pain, followed by paralysis Diarrhea, repeated Vomit, thirst, eye burning sensation, and then acute death. Rat oral LD50 95rng/kg. Rat LC32 x 10-6 in air. The maximum allowable concentration in workplace air is 5 × 10-6. In order to prevent poisoning, the equipment should be closed, the production site requires good ventilation, the operator should wear masks, gloves and other protective equipment. But rubber gloves can not play a protective role, because the chlorine ethanol through the rubber gloves and skin contact and cause harm. If the clothing is stained with ethyl chloride should be immediately removed, the skin stained with ethyl chloride after washing with soap, then rinse with plenty of water.
  • generally, it is transported by tank car, and impact should be avoided. Can also be packed in iron barrels, 200kg per barrel. Prevents direct contact and vapor exosmosis. According to the provisions of toxic substances storage and transportation.
Last Update:2022-01-01 10:15:36

ethylene glycol, chlorohydrin - Reference Information

LogP-0.06-1.06 at 20℃
NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
use used in the manufacture of ethylene oxide, synthetic rubber, dyes, medicines and pesticides, etc., and also used as an organic solvent
chloroethanol is an important organic solvent and organic synthesis raw material. In the past, the biggest use of chloroethanol was to produce ethylene oxide. Now most of the chlorohydrin ethylene oxide devices have been replaced by direct oxidation. Now the main use of chloroethanol is as a raw material for polysulfide rubber and as an intermediate for dyes, pesticides, and medicines. Thiodiethylene glycol can be obtained by the reaction of chloroethanol and sodium sulfide. It is a printing and dyeing solvent for textiles, as well as a vat dye and a plasticizer for polysubunit dichloride. Chloroethanol derivative β, β'dichlorodiethyl ether is the raw material for the synthesis of mustard gas, and it is also an extraction solvent for refined lubricating oil. It is also used as a soil fungicide. Chloroethanol can synthesize dichloroethyl formaldehyde and is one of the raw materials for the production of polysulfide elastomers. The reaction of chloroethanol and acetylene can produce chloroethyl vinyl ether, which is the raw material for the formation of polypropylene acidic body. Chloroethanol is oxidized with 60% nitric acid to produce chloroacetic acid in 90% yield, which is used to synthesize dyes, aminoacetic acid, malonate, glycolic acid, epinephrine, 2,4-dichlorophenoxyacetic acid, dimethoate, carboxymethyl Cellulose, Felonar sleeping pills, chloroacetamide, iodoacetamide, sodium N-methylaminoacetate. In the pharmaceutical industry, chloroethanol is used in the production of piperazine phosphate, furazolidone, tetramidazole, procaine and procaine, and is used as a raw material for pesticide 1059 in pesticide production. 2-Chloroethylamine hydrochloride ([870-24-6],Beil can be obtained by ammoniation and chlorination of chloroethanol. 4,133), which is a pharmaceutical intermediate used to make deworming net.
Used in the manufacture of ethylene oxide, synthetic rubber, dyes, medicines and pesticides, etc., and also organic solvents
Used as solvents, pesticides and sugarcane germination agents, etc., and also used in the synthesis of pesticides and dyes
production method there are many preparation methods for chloroethanol. The reaction of ethylene oxide with hydrochloric acid is the most convenient method for preparing chloroethanol in the laboratory. In fact, the reaction of ethylene glycol and sulfur dichloride to obtain chloroethanol is also one of the methods for preparing chloroethanol in the laboratory. If ethylene oxide reacts with anhydrous hydrogen chloride in the presence of ferric chloride and sodium dihydrogen phosphate, no by-product ethylene glycol is generated, which is suitable for manufacturing high-purity chloroethanol. The industrial production method of chloroethanol is basically the method proposed by the Gomberg in 1991. Ethylene and chlorine are simultaneously introduced into water, and chlorine reacts with water to form hypochlorous acid. The addition of hypochlorous acid and ethylene yields chloroethanol.
category pesticide
toxicity classification highly toxic
acute toxicity oral-rat LD50: 71 mg/kg; Oral-mouse LD50: 81 mg/kg
stimulation data skin-rabbit 200 mg/2 h mild; Eye-rabbit 9 mg/6 h moderate
explosive hazard characteristics blastable when mixed with air
flammability hazard characteristics open flame, high temperature, strong oxidant combustible; highly toxic phosgene and chloride smoke generated by high heat decomposition
storage and transportation characteristics warehouse ventilation and low temperature drying; Store separately from oxidants and food additives
fire extinguishing agent foam, carbon dioxide, yellow sand
occupational standard TWA 5 PPM (16 mg/m3); STEL 1 PPM (3 mg/m3)
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
immediate life-threatening and health concentration 7 ppm
Last Update:2024-04-09 15:16:47
ethylene glycol, chlorohydrin
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CAS: 107-07-3
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View History
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Raw Materials for ethylene glycol, chlorohydrin
Ethylene Oxide
Hydrochloric acid
Downstream Products for ethylene glycol, chlorohydrin
1-Bromo-2-fluoroethane
Choline chloride
trihydroxyethylrutin
diphenhydramine
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