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Diethylaluminum chloride
[CAS# 96-10-6]

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Complete supplier list of Diethylaluminum chloride
Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrimidine compound >> Aldehyde intermediate
Name Diethylaluminum chloride
Molecular Structure CAS # 96-10-6, Diethylaluminum chloride
Molecular Formula C4H10AlCl
Molecular Weight 120.56
CAS Registry Number 96-10-6
EC Number 202-477-2
SMILES CC[Al](CC)Cl
Properties
Density 0.887 g/mL (25 ºC)
Melting point -85 ºC
Flash point -18 ºC
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS05 Danger    Details
Hazard Statements H225-H250-H260-H21-H314-H318    Details
Precautionary Statements P210-P222-P223-P231-P231+P232-P233-P240-P241-P242-P243-P260-P264-P264+P265-P280-P301+P330+P331-P302+P335+P334-P302+P361+P354-P303+P361+P353-P304+P340-P305+P354+P338-P316-P317-P321-P363-P370+P378-P402+P404-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Pyrophoric liquidsPyr. Liq.1H250
Skin corrosionSkin Corr.1BH314
Substances or mixtures which in contact with water emit flammable gasesWater-react.1H260
Serious eye damageEye Dam.1H318
Flammable liquidsFlam. Liq.2H225
Substances or mixtures which in contact with water emit flammable gasesWater-react.2H261
Skin corrosionSkin Corr.1AH314
Self-heating substances or mixturesSelf-heat.2H252
Specific target organ toxicity - repeated exposureSTOT RE1H372
Aspiration hazardAsp. Tox.1H304
Specific target organ toxicity - single exposureSTOT SE3H335
Reproductive toxicityRepr.2H361
Skin corrosionSkin Corr.1H314
Transport Information UN 3394
SDS Available
up Discovory and Applicatios
Diethylaluminum chloride (DEAC) is a valuable organoaluminum compound known for its unique chemical properties and wide range of applications in various industries. Its discovery and usefulness have made it an important substance in modern chemistry and materials science.

Diethylaluminum chloride was first synthesized in the early 20th century as part of research on organometallic compounds. The compound is an organoaluminum reagent with the chemical formula C₄H₁₀AlCl. It was originally developed to explore its potential as a catalyst and reagent in organic synthesis. Over time, its unique reactivity and role in polymer chemistry were recognized, leading to its widespread application.

DEAC is a colorless to pale yellow liquid with a pungent odor. It is highly reactive and sensitive to moisture, forming hydrochloric acid and aluminum hydroxide upon contact with water. The compound has a boiling point of 71°C and is soluble in organic solvents such as benzene and toluene. Its reactivity and solubility properties make it a valuable tool in chemical synthesis.

Diethylaluminum chloride is widely used as a catalyst for olefin polymerization, especially in the production of polyethylene and other high-performance polymers. It acts as a co-catalyst along with other compounds to facilitate the polymerization process and enhance the properties of the resulting material.

In organic chemistry, DEAC is used as a reagent for a variety of chemical transformations. It is used to synthesize complex organic molecules, including pharmaceuticals and fine chemicals. Its ability to react with a wide range of substrates makes it a versatile tool in synthetic chemistry.

The compound functions in hydroformylation reactions, where it acts as a catalyst to convert olefins into aldehydes. This process is important for the production of a variety of aldehydes used in the manufacture of detergents, plasticizers, and other industrial chemicals.

DEAC is used in surface treatment applications to modify the properties of metals and other materials. It helps improve the adhesion and bonding of coatings and can improve the durability and performance of surface treatments.

Diethylaluminum chloride is used in research laboratories to study its reactivity and applications. Its role as a reagent and catalyst provides valuable insights into chemical reaction mechanisms and the development of new materials.

Ongoing research focuses on optimizing the use of DEAC in various industrial processes and exploring new applications. Innovations in catalyst design and green chemistry are expected to improve the efficiency and sustainability of DEAC-based processes.
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