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Aluminum, diethylphenoxy-, also known as diethylphenoxyaluminum, is a chemical compound with the formula (C2H5)2Al(OC6H5). It is a colorless, oily liquid that is soluble in organic solvents. This organoaluminum compound is primarily used as a catalyst in various chemical reactions, particularly in the polymerization of olefins and the production of polyethylene. It is also employed as a cocatalyst in the Ziegler-Natta catalyst system for the synthesis of polyolefins. Due to its reactivity, it is typically handled under an inert atmosphere to prevent unwanted side reactions.

13235-18-2

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13235-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13235-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13235-18:
(7*1)+(6*3)+(5*2)+(4*3)+(3*5)+(2*1)+(1*8)=72
72 % 10 = 2
So 13235-18-2 is a valid CAS Registry Number.

13235-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl(phenoxy)alumane

1.2 Other means of identification

Product number -
Other names Diaethylaluminiumphenolat

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:13235-18-2 SDS

13235-18-2Downstream Products

13235-18-2Relevant academic research and scientific papers

PHENOXYALUMINIUM COMPOUNDS. VI. COMPLEX AND REACTION MECHANISM OF METHYLALUMINIUM COMPOUNDS WITH ANISOLE

Starowieyski, K. B.,Rzepkowska, Z.

, p. 309 - 320 (2007/10/02)

The reactions of anisole with organoaluminium compounds MenAlXn-1 have been investigated.The formation of a complex is the first reaction step, followed by cleavage and elimination of the gases MeX and small amounts of hydrocarbons.The yield of the gases and the cleavage rate decreases in the order: AlCl3>/=MeAlCl2>Me2AlCl>>Me3Al and Me2AlI>Me2AlCl>Me2AlBr.For most of the investigated reaction a marked decrease in gas evolution was observed after a short period of time.This is explained by the formation of an almost inactive mixed dimer (I) which at the (I) reaction temperature is more stable than the Me2(Cl)Al:O(Me)Ph complex.It is suggested that dimer I is formed after the intramolecular reaction of the 2:1 complex II after elimination of MeX. (II).

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