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8-[3-(8-hydroxyoctyl)oxiran-2-yl]octanoic acid is a complex organic compound with the molecular formula C16H30O5. It is characterized by a long hydrocarbon chain with an oxirane (epoxide) group and a hydroxyl group, which are key functional groups in chemical reactions. 8-[3-(8-hydroxyoctyl)oxiran-2-yl]octanoic acid is known for its potential applications in the synthesis of various pharmaceuticals and industrial chemicals due to its unique structure. The presence of the epoxide ring makes it a valuable intermediate in the preparation of compounds with specific reactivity and selectivity. The hydroxyl group further enhances its versatility, allowing for the formation of esters, ethers, and other derivatives. Its structure also suggests potential use in the development of surfactants or as a building block for more complex molecules.

3233-92-9

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3233-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3233-92-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3233-92:
(6*3)+(5*2)+(4*3)+(3*3)+(2*9)+(1*2)=69
69 % 10 = 9
So 3233-92-9 is a valid CAS Registry Number.

3233-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-[3-(8-hydroxyoctyl)oxiran-2-yl]octanoic acid

1.2 Other means of identification

Product number -
Other names 18-hydroxy-9,10-epoxyoctadecanoic acid

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:3233-92-9 SDS

3233-92-9Upstream product

3233-92-9Downstream Products

3233-92-9Relevant academic research and scientific papers

Unveiling the dual role of the cholinium hexanoate ionic liquid as solvent and catalyst in suberin depolymerisation

Ferreira, Rui,Garcia, Helga,Sousa, Andreia F.,Guerreiro, Marina,Duarte, Filipe J. S.,Freire, Carmen S. R.,Calhorda, Maria Jose,Silvestre, Armando J. D.,Kunz, Werner,Rebelo, Luis Paulo N.,Silva Pereira, Cristina

, p. 2993 - 3002 (2014/01/06)

Disruption of the three-dimensional network of suberin in cork by cholinium hexanoate leads to its efficient and selective isolation. The reaction mechanism, which likely involves selective cleavage of some inter-monomeric bonds in suberin, was still unanswered. To address this question, the role of the ionic liquid during suberin depolymerisation and during cleavage of standard compounds carrying key chemical functionalities was herein investigated. A clear demonstration that the ionic liquid catalyses the hydrolysis of acylglycerol ester bonds was attained herein, both experimentally and computationally (DFT calculations). This behaviour is related to cholinium hexanoate capacity to activate the nucleophilic attack of water. The data showed also that the most favourable reaction is the hydrolysis of acylglycerol ester bonds, with the C2 position reporting the faster kinetics, whilst most of the linear aliphatic esters remained intact. The study emphasises that the ionic liquid plays the dual role of solvent and catalyst and leads to suberin efficient extraction through a mild depolymerisation. It is also one of the few reports of ionic liquids as efficient catalysts in the hydrolysis of esters.

DEPOLYMERIZATION EXTRACTION OF COMPOUNDS FROM BIRCH BARK

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Page/Page column 37; 44, (2008/06/13)

The invention provides improved processes for the extraction of betulin, lupeol, betulinic acid, suberinic acids, and/or other organic compounds and compositions from birch bark.

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