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25364-52-7

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25364-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25364-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,6 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25364-52:
(7*2)+(6*5)+(5*3)+(4*6)+(3*4)+(2*5)+(1*2)=107
107 % 10 = 7
So 25364-52-7 is a valid CAS Registry Number.

25364-52-7SDS

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 2,2,3,3-tetramethyl-oxetane

1.2 Other means of identification

Product number -
Other names 2.2.3.3-Tetramethyloxetan

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:25364-52-7 SDS

25364-52-7Upstream product

25364-52-7Downstream Products

25364-52-7Relevant articles and documents

Addition of 2,2,3-Trimethylbutane to Slowly Reacting Mixtures of Hydrogen and Oxygen at 480 deg C

Baldwin, Roy R.,Walker, Raymond W.,Walker, Robert W.

, p. 2157 - 2174 (1981)

The oxidation of 2,2,3-trimethylbutane(TRIMB) has been studied by adding traces of the alkane to slowly reacting mixtures of H2+O2 in aged boric-acid-coated vessels at 480 deg C.Rate constants for H and OH attack on TRIMB have been obtained and, by use of an additivity principle, Arrhenius parameters of log10(A/dm3mol-1s-1)=9.32+/-0.13 and E=460+/-950 J mol-1 are suggested for OH attack at a tertiary C-H bond in alkanes from a combination of the present results with studies at lower temperatures.Propene, isobutene, and 2,2,3-trimethylbut-1-ene (TRIMB-1) are the major initial products, the yield of the latter increasing markedly at high O2 pressures.The proportions of the three species of trimethylbutyl radicals formed in each mixture have been estimated.Two of the species of trimethylbutyl radicals react almost completely by homolysis of the strained central C-C bond to give propene and isobutene as products.The tird radical (CH3)3CC(CH3)2 is removed by either reaction (1C) or (2C), and it is suggested that (1C) occurs by a concerted mechanism: (CH3)3CC(CH3)2 i-C4H8 + i-C3H7 (1C) (CH3)3CC(CH3)2 + O2 (CH3)3CC(CH3)=CH2 + HO2. (2C) Rate constants have been obtained for a number of the homolysis reactions of the trimethylbutyl radicals, for which there is a good correlation between log k and ΔU, the internal energy change.

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