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2-Chloroethanol
[CAS# 107-07-3]

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Complete supplier list of 2-Chloroethanol
Identification
Classification Organic raw materials >> Alcohols, phenols, phenolic compounds and derivatives >> Halogenated, sulfonated, nitrated or nitrosated derivatives of alcohols
Name 2-Chloroethanol
Synonyms Ethylene chlorohydrin
Molecular Structure CAS # 107-07-3, 2-Chloroethanol, Ethylene chlorohydrin
Molecular Formula C2H5ClO
Molecular Weight 80.51
CAS Registry Number 107-07-3
EC Number 203-459-7
SMILES C(CCl)O
Properties
Density 1.201
Melting point -63 ºC
Boiling point 129 ºC
Refractive index 1.4405-1.4425
Flash point 55 ºC
Water solubility MISCIBLE
Safety Data
Hazard Symbols symbol   GHS06 Danger    Details
Hazard Statements H310-H330-H300    Details
Precautionary Statements P210-P233-P234-P240-P241-P242-P243-P260-P262-P264-P264+P265-P270-P271-P273-P280-P284-P301+P316-P302+P352-P303+P361+P353-P304+P340-P305+P354+P338-P316-P317-P320-P321-P330-P361+P364-P370+P378-P390-P391-P403+P233-P403+P235-P405-P406-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.1H310
Acute toxicityAcute Tox.2H300
Flammable liquidsFlam. Liq.3H226
Serious eye damageEye Dam.1H318
Substances or mixtures corrosive to metalsMet. Corr.1H290
Acute toxicityAcute Tox.1H330
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.2H330
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Transport Information UN 1135
SDS Available
up Discovory and Applicatios
2-Chloroethanol, also known as ethylene chlorohydrin, is a simple chlorinated alcohol with the molecular formula C2H5ClO. Its discovery dates back to the early 19th century during research on alcohol derivatives. The compound was identified as a byproduct in various chemical reactions involving ethylene and chlorine, marking its importance in the chemical industry. With its reactive hydroxyl group and chlorine atom, 2-chloroethanol plays a pivotal role as a chemical intermediate, particularly in the synthesis of larger molecules.

One of the primary applications of 2-chloroethanol is in the production of ethylene oxide, a significant industrial chemical used to manufacture a variety of products including antifreeze, detergents, and solvents. 2-Chloroethanol reacts with a base, typically sodium hydroxide, to yield ethylene oxide through an intramolecular cyclization process. This reaction has been widely used in industrial processes for the large-scale production of ethylene oxide, which in turn serves as a precursor for producing ethylene glycol.

Another key application of 2-chloroethanol is its use in the preparation of pharmaceuticals and agrochemicals. It serves as an intermediate in the synthesis of compounds with biologically active properties, including pesticides, herbicides, and certain pharmaceutical agents. Its ability to introduce a reactive chloroethyl group into organic molecules has been exploited in the production of specialty chemicals that require specific structural features.

In the realm of organic synthesis, 2-chloroethanol can be used as an alkylating agent. Its reactivity allows it to introduce ethoxy groups into various chemical structures, thereby enabling the modification of molecular frameworks in both research and industrial chemistry. Additionally, it has found applications in the production of plasticizers and surfactants, where it acts as a building block for more complex chemicals.

While 2-chloroethanol has proven valuable in industrial and chemical applications, it is important to note that it is a toxic and potentially hazardous substance. Its harmful effects on human health are primarily due to its irritant and neurotoxic properties. Inhalation or dermal exposure can lead to symptoms such as dizziness, headaches, and respiratory distress. Consequently, strict handling and safety protocols are in place when working with 2-chloroethanol, particularly in industrial settings.

Despite these hazards, 2-chloroethanol remains a crucial component in various chemical industries due to its versatility as a chemical intermediate. Its ability to contribute to the synthesis of diverse compounds, from pharmaceuticals to industrial chemicals, underscores its significance in modern chemistry.
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