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760-19-0

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760-19-0 Usage

Description

BROMODIETHYLALUMINUM, also known as Ethylaluminum dichloride, is an aluminum alkyl halide with the chemical formula (C2H5)2AlCl. It is a flammable, reactive, and potentially spontaneously combustible compound in air, with a colorless to yellow liquid appearance. Its chemical properties make it a versatile reagent in various industrial applications.

Uses

Used in Chemical Synthesis:
BROMODIETHYLALUMINUM is used as a reagent for [initiating polymerization reactions] because of its high reactivity and ability to initiate polymerization of olefins and dienes, which is crucial in the production of various polymers.
Used in Petrochemical Industry:
BROMODIETHYLALUMINUM is used as a catalyst for [olefin polymerization] in the petrochemical industry, where it plays a vital role in the production of polyethylene and other related polymers.
Used in Organometallic Chemistry:
BROMODIETHYLALUMINUM is used as a precursor for [organometallic compounds] in organometallic chemistry, where it can be used to synthesize a wide range of organoaluminum compounds with various applications.
Used in Research and Development:
BROMODIETHYLALUMINUM is used as a research compound for [exploring new chemical reactions and applications] due to its unique reactivity and potential for discovering new synthetic pathways and applications in various fields.

Potential Exposure

These materials are used as components of olefin polymerization catalysts. The reader is referred to the entry on “Aluminum alkyls” for additional information on this entry. The aluminum alkyl halides parallel very closely the aluminum alkyls

Shipping

UN3052 Spontaneously combustible. Water reactive releasing large quantities of toxic and deadly hydrogen gas. (Note: this number does not appear in the 49/CFR HazMat tables)

Incompatibilities

The aluminum alkyl halides are strong reducing agents; they react—possibly violently—with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. These chemicals react violently with nitromethaneEthylaluminum sesquichloride reacts explosively with carbon tetrachloride at room temperature. This chemical reacts violently with water, forming corrosive hydrogen chloride and flammable ethane gas. Diethylaluminum chloride may form an explosive product with chlorine azide.

Check Digit Verification of cas no

The CAS Registry Mumber 760-19-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 760-19:
(5*7)+(4*6)+(3*0)+(2*1)+(1*9)=70
70 % 10 = 0
So 760-19-0 is a valid CAS Registry Number.
InChI:InChI=1/2C2H5.Al.BrH/c2*1-2;;/h2*1H2,2H3;;1H/q2*-1;+3;/p-1

760-19-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bromo(diethyl)alumane

1.2 Other means of identification

Product number -
Other names BROMODIETHYLALUMINUM

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:760-19-0 SDS

760-19-0Relevant articles and documents

Lewis acid-assisted detection of nerve agents in water

Butala, Rahul R.,Creasy, William R.,Fry, Roderick A.,McKee, Michael L.,Atwood, David A.

supporting information, p. 9269 - 9271 (2015/06/08)

The five-coordinate compound, Salen(tBu)Al(Ac), prepared in situ from Salen(tBu)AlBr and NH4Ac, forms Lewis acid-base adducts in aqueous solution with the G-type nerve agents, Sarin and Soman, and the VX hydrolysis product, ethylmethylphosphonate (EMPA). The resulting compounds, [Salen(tBu)Al(NA)]+[Ac] - (with NA = Sarin, Soman, and EMPA) are sufficiently stable to be identified by ESI-MS. Molecular ion peaks were detected for every compound with little or no fragmentation. The distinctive MS signatures for the [Salen(tBu)Al(NA)]+ compounds provide a new technique for identifying nerve agents from aqueous solution. The energetics of the displacement of Ac- by the nerve agents to form [Salen(tBu)Al(NA)]+[Ac]- were determined computationally.

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