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4-(butylsulfanyl)butan-1-ol is an organic compound with the molecular formula C8H18OS. It is a colorless liquid with a distinct odor and is soluble in water. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known as 4-(n-butylthio)butanol or 4-butylsulfanylbutan-1-ol. The compound is characterized by its butylsulfanyl group attached to a butan-1-ol backbone, which contributes to its unique chemical properties and reactivity. It is important to handle 4-(butylsulfanyl)butan-1-ol with care due to its potential irritant and toxic nature, and it should be stored away from heat and open flames.

5331-34-0

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5331-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5331-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5331-34:
(6*5)+(5*3)+(4*3)+(3*1)+(2*3)+(1*4)=70
70 % 10 = 0
So 5331-34-0 is a valid CAS Registry Number.

5331-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-butylsulfanylbutan-1-ol

1.2 Other means of identification

Product number -
Other names n-butyl 4-hydroxybutyl sulfide

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:5331-34-0 SDS

5331-34-0Downstream Products

5331-34-0Relevant academic research and scientific papers

Formation of cyclic sulfonium salts by Me3SiI-promoted intramolecular displacement of hydroxide or methoxide by sulfide. Ring contraction thiepane → thiolane

Cere, Vanda,Pollicino, Salvatore,Fava, Antonino

, p. 5989 - 5998 (2007/10/03)

A suitably positioned (1,2-, 1,4-, and 1,5-) intramolecular sulfide interferes with the iodotrimethylsilane-promoted iodine for hydroxyl substitution, as well as the related alcohol deprotection procedure (regioselective cleavage of methyl ethers). The ou

Et3B Induced Radical Addition of Thiols to Acetylenes

Ichinose, Yoshifumi,Wakamatsu, Kuni,Nozaki, Kyoko,Birbaum, Jean-Luc,Oshima,Koichiro,Utimoto, Kiitiro

, p. 1647 - 1650 (2007/10/02)

Thiols added easily to acetylenic compounds in the presence of Et3B to give alkenyl sulfides in good yields.The reaction of acetylenes with 3-methyl-2-buten-1-thiol gave dihydrothiophene derivatives in one pot.

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