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147794-11-4

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147794-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147794-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,9 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147794-11:
(8*1)+(7*4)+(6*7)+(5*7)+(4*9)+(3*4)+(2*1)+(1*1)=164
164 % 10 = 4
So 147794-11-4 is a valid CAS Registry Number.

147794-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxybutyl nitrate

1.2 Other means of identification

Product number -
Other names 1-Nitrooxy-2-butanol

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:147794-11-4 SDS

147794-11-4Downstream Products

147794-11-4Relevant articles and documents

Determination of the hydroxy nitrate yields from the reaction of C2-C6 alkenes with OH in the presence of NO

O'Brien, Jason M.,Czuba, Eva,Hastie, Donald R.,Francisco, Joseph S.,Shepson, Paul B.

, p. 8903 - 8908 (1998)

The yields of hydroxy nitrates from the reaction of selected C2-C6 alkenes with OH in the presence of NO were measured at 296 ± 3 K in a 9600 L photochemical smog chamber. Hydroxyl radicals were produced from the photolysis of isopropyl nitrite in the presence of NO. The loss of the alkene was followed using gas chromatography. The hydroxy nitrate products were determined using a combination of capillary chromatography and an organic nitrate specific chemiluminescence detector. The yield of hydroxy nitrates was observed to increase with the size of the precursor alkene as follows: ethene (0.86%), propene (1.5%), 1-butene (25%), cis-2-butene (3.4%), and 1-hexene (5.5%). Previous studies involving the production of alkyl nitrates from alkanes show a similar trend, but the yields reported here are a factor of 2-3 lower than for the corresponding simple alkylperoxy radical. The impact of a β-hydroxy group on the nitrate yield is examined using an ab initio molecular orbital study. It indicates that a hydrogen-bonded peroxy nitrite intermediate is formed, which results in a decrease in D0(O-O) for the peroxy linkage of about 8 kJ/mol. This would be expected to effectively decrease the organic nitrate yield. The implications of these findings for the organic nitrate path as an atmospheric NOx removal mechanism are discussed.

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