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Butylsec-butylsulfide, with the molecular formula C8H18S, is an organic sulfide known for its colorless to pale yellow liquid form and a strong garlic-like odor. It is recognized for its use as a flavor and fragrance additive, as well as a precursor in the synthesis of pharmaceutical and agrochemical products. Despite its low toxicity, it can cause irritation to the skin, eyes, and respiratory system upon exposure.

10359-61-2

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10359-61-2 Usage

Uses

Used in Flavor and Fragrance Industry:
Butylsec-butylsulfide is used as a flavoring and fragrance agent for its strong garlic-like odor, adding distinctive scents to various products in the food and cosmetic industries.
Used in Pharmaceutical Industry:
Butylsec-butylsulfide is used as a precursor in the synthesis of pharmaceutical products, contributing to the development of new medications and compounds.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, Butylsec-butylsulfide serves as a precursor in the synthesis of agrochemical products, aiding in the creation of substances for agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10359-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10359-61:
(7*1)+(6*0)+(5*3)+(4*5)+(3*9)+(2*6)+(1*1)=82
82 % 10 = 2
So 10359-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H18S/c1-4-6-7-9-8(3)5-2/h8H,4-7H2,1-3H3

10359-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butan-2-ylsulfanylbutane

1.2 Other means of identification

Product number -
Other names 3-methyl-4-thiaoctane

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:10359-61-2 SDS

10359-61-2Downstream Products

10359-61-2Relevant academic research and scientific papers

The kinetics of thiyl radical-induced reactions of monounsaturated fatty acid esters

Chatgilialoglu, Chryssostomos,Altieri, Alessio,Fischer, Hanns

, p. 12816 - 12823 (2002)

The time-dependent isomerizations and thiol additions of several Z- and E-monounsaturated fatty acid methyl esters catalyzed by alkanethiyl radicals during γ-radiolysis of tert-butyl alcohol solutions are analyzed on the basis of the radiation chemical yield of radicals and established rate data. This provides room-temperature rate constants for the reversible thiyl addition. Within experimental errors, they do not depend on the double bond position in the alkyl chains. Particularly noteworthy is the very fast β-elimination of thiyl radicals from alkyl radicals which carry a second β-substituent. It is supported by additional evidence obtained with a radical clock methodology, and the large preference of fragmentation to the E-isomers is attributed to different barriers for the formation of the E- and Z-transition states from the equilibrium radical structure.

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