2114-18-3

Basic information

• Product Name: 2-Chloroethyl carbamate
• Synonyms: B-CHLOROETHYL CARBAMATE;BETA-CHLOROETHYLURETHANE;BETA-CHLOROETHYL CARBAMATE;2-CHLOROETHYL CARBAMATE;Carbamic acid, beta-chloroethyl ester;carbamicacid,2-chloroethylester;carbamicacid,beta-chloroethylester;Chloroethyl carbamate
• CAS NO: 2114-18-3
• Molecular Formula: C₃H₆ClNO₂
• Molecular Weight: 123.54
• EINECS: 218-310-1
• Mol File: 2114-18-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 74-77 °C(lit.)
• Boiling Point: 264.3 °C at 760 mmHg
• Flash Point: 113.7 °C
• Appearance: /
• Density: 1.2776 (rough estimate)
• Vapor Pressure: 0.00976mmHg at 25°C
• Refractive Index: 1.5000 (estimate)
• PKA: 13.18±0.50(Predicted)
• CAS DataBase Reference: 2-Chloroethyl carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloroethyl carbamate(2114-18-3)
• EPA Substance Registry System: 2-Chloroethyl carbamate(2114-18-3)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 36/37/39-45
• WGK Germany: 3
• RTECS: EZ1475000
• Hazardous Substances Data: 2114-18-3(Hazardous Substances Data)

Usage

General Description

2-Chloroethyl carbamate is a chemical compound that falls under the category of carbamates, which are organic compounds commonly used in various industries such as agriculture and medicine. It is known for its reactivity as it can undergo several reactions to form different organic compounds. It is usually in solid form and its potential applications include being used as a pesticide, pharmacological agent, and even in the production of certain synthetic materials. Like many carbamates, 2-Chloroethyl carbamate's toxicity levels and potential hazards to humans and the environment depend on factors such as exposure levels and method of contact. Therefore, proper handling and safety measures are needed while dealing with this chemical.

InChI:InChI=1/C3H6ClNO2/c4-1-2-7-3(5)6/h1-2H2,(H2,5,6)

Upstream product

• 5395-01-7 2-hydroxyethyl carbamate 
• 75-09-2 dichloromethane 
• 107-21-1 ethylene glycol 
• 506-77-4 cyanogen chloride 
• 627-11-2 2-Chloroethyl chloroformate 
• 463-72-9 carbamic chloride 
• 107-07-3 2-chloro-ethanol 
• 21832-34-8 sulfinylcarbamic acid 2-chloro-ethyl ester 
• 917-61-3 sodium isocyanate 

Downstream Products

• 64038-81-9 4-(2-carbamoyloxy-ethyl)-4-methyl-morpholinium; chloride 
• 94392-36-6 iodoethyl carbamate 
• 100614-68-4 N,N'-benzylidene-bis-carbamic acid bis-(2-chloro-ethyl ester) 
• 4220-32-0 Dimethylaminoethyl carbamate 
• 51-83-2 carbachol 
• 75-21-8 oxirane 
• 590-28-3 potassium cyanate 

Relevant articles and documents

PREPARATION OF CARBAMATES

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New chloro-meta-phenylenediamines, their use as couplers in the oxidation dyeing of keratinous fibres, dyeing compositions for hair containing these compounds and dyeing process using the said

New chloro-meta-phenylenediamines, their use as couplers in the oxidation dyeing of keratinous fibres, dyeing compositions for hair containing these compounds and dyeing process using the said compositions. The invention relates to the compounds of formula: STR1 in which Z and Z' denote, independently of one another, an alkyl radical having from 1 to 4 carbon atoms or a hydroxyalkyl radical having from 2 to 4 carbon atoms, and R1 and R2 denote, independently of one another, a hydrogen atom, an alkyl radical having from 1 to 4 carbon atoms or a mono- or polyhydroxyalkyl radical having 2 or 3 carbon atoms, to their addition salts with an acid, and to their use by way of couplers for the oxidation dyeing of keratinous fibres, especially human hair. These compounds, when they are combined with paraphenylenediamines, surprisingly give beige to light brown hues or purple hues of greater or lesser redness, depending on the substitution of the 5-amino group of the chlorobenzene.