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Octyl-2-hydroxyethylsulfoxide, also known as 2-(octylsulfinyl)ethanol, is an organic compound with the chemical formula C10H22O2S. It is a colorless liquid with a molecular weight of 206.35 g/mol. octyl-2-hydroxyethylsulfoxide is characterized by the presence of an octyl group (an eight-carbon alkyl chain) attached to a sulfoxide functional group, which consists of a sulfur atom bonded to an oxygen atom and an alkyl group. Octyl-2-hydroxyethylsulfoxide is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a surfactant and a stabilizer in various industrial applications. Due to its unique chemical structure, it exhibits properties such as solubility in organic solvents and reactivity with nucleophiles, making it a valuable building block in organic synthesis.

7305-30-8

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7305-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7305-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7305-30:
(6*7)+(5*3)+(4*0)+(3*5)+(2*3)+(1*0)=78
78 % 10 = 8
So 7305-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O2S/c1-2-3-4-5-6-7-9-13(12)10-8-11/h11H,2-10H2,1H3

7305-30-8SDS

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-(Octylsulfinyl)ethanol (OSE)

1.2 Other means of identification

Product number -
Other names 2-HYDROXYETHYLOCTYLSULFOXIDE

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:7305-30-8 SDS

7305-30-8Relevant academic research and scientific papers

REACTIONS OF OXIRANES WITH ALKYLTHIOLS

Chlebicki, Jan,Cichacz, Zbigniew

, p. 485 - 494 (2007/10/02)

Alkyl-2-hydroxyalkyl sulfides and their oxyalkylenated adducts were obtained in the reaction of oxirane or methyloxirane with C4-C12 alkylthiols in presence of basic or acidic catalysts.The sulfides were further oxidized to sulfoxides and sulfones.

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