367-44-2 Usage
Uses
Used in Plastics Industry:
DIETHYL ALUMINUM FLUORIDE is used as a catalyst for the production of high-density polyethylene and polypropylene, which are essential materials in the manufacturing of various plastic products. Its role in these processes is crucial for achieving the desired properties and characteristics of the end products.
Used in Chemical Catalysts:
In the field of chemical catalysis, DIETHYL ALUMINUM FLUORIDE is employed as a co-catalyst in Ziegler-Natta polymerization processes. This application is vital for facilitating and enhancing the efficiency of these chemical reactions, leading to the production of polymers with specific properties tailored to various applications.
Used in Research and Development:
DIETHYL ALUMINUM FLUORIDE also finds use in research and development settings, where its unique catalytic and co-catalytic properties are explored and harnessed for the creation of new materials and the improvement of existing processes. This contributes to the advancement of various industries, including plastics, chemicals, and materials science.
Safety Measures:
Given the reactive and flammable nature of DIETHYL ALUMINUM FLUORIDE, it is imperative to implement proper safety measures when working with this chemical. This includes the use of personal protective equipment, such as gloves, goggles, and respirators, to minimize the risk of skin and eye irritation, as well as respiratory and digestive tract issues. Additionally, proper ventilation systems should be in place to prevent the accumulation of harmful vapors and ensure a safe working environment.
Check Digit Verification of cas no
The CAS Registry Mumber 367-44-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 367-44:
(5*3)+(4*6)+(3*7)+(2*4)+(1*4)=72
72 % 10 = 2
So 367-44-2 is a valid CAS Registry Number.
InChI:InChI=1/2C2H5.Al.FH/c2*1-2;;/h2*1H2,2H3;;1H/q2*-1;+3;/p-1
367-44-2Relevant academic research and scientific papers
Laubengayer,Lengnick
, p. 503 - 507 (1966)
The unusually viscous compound diethylfluoroalane, (C2H5)2AlF, has been characterized. Cryoscopic and ebullioscopic molecular weight determinations in benzene solution indicate the existence of a tetramer. Infrared, pmr, and F19 nmr spectra support a ring structure, with an alternating aluminum-fluorine backbone for the tetramer. The compound has acceptor properties weaker than those of the other dialkylhaloalanes. No stable ether adduct could be isolated, but the identity of amine adducts and their decomposition products has been established. Pyrolytic decomposition of (C2H5)2AlF yields ethane, in contrast to the olefins which have been reported for other alkylaluminum compounds. The high viscosity of liquid (C2H5)2AlF is believed to result from extensive Al-F-Al bridging to build polymeric frameworks. Copyright 1966 by the American Chemical Society.
