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3-Methyl-1-butanethiol is an organic compound with a distinct, strong, and pungent odor. It is a clear colorless to slightly yellow liquid at room temperature and is known for its low aroma threshold value, which makes it easily detectable even at very low concentrations.

541-31-1

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541-31-1 Usage

Uses

Used in Flavor Industry:
3-Methyl-1-butanethiol is used as a flavoring agent for its characteristic strong, pungent odor. It is commonly employed in the creation of artificial flavors, particularly those mimicking the aroma of cooked or roasted foods, due to its ability to replicate the smell of sulfur-containing compounds that are naturally present in these types of food.
Used in Beer Production:
In the beer industry, 3-Methyl-1-butanethiol is used to add a desirable complexity to the aroma profile of certain beer types. Its presence, even in trace amounts, can contribute to the overall flavor and character of the beer, making it an important component in the brewing process.
Used in Chemical Synthesis:
3-Methyl-1-butanethiol can also be used as a starting material or intermediate in the synthesis of various organic compounds, particularly those with sulfur-containing functional groups. Its unique chemical properties make it a valuable building block in the development of new chemicals and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 541-31-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 541-31:
(5*5)+(4*4)+(3*1)+(2*3)+(1*1)=51
51 % 10 = 1
So 541-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H12S/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H3

541-31-1 Well-known Company Product Price

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  • Alfa Aesar

  • (L09661)  Isopentyl mercaptan, 97%   

  • 541-31-1

  • 25ml

  • 925.0CNY

  • Detail
  • Alfa Aesar

  • (L09661)  Isopentyl mercaptan, 97%   

  • 541-31-1

  • 100ml

  • 2979.0CNY

  • Detail
  • Aldrich

  • (115924)  3-Methyl-1-butanethiol  97%

  • 541-31-1

  • 115924-5G

  • 379.08CNY

  • Detail

541-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-1-butanethiol

1.2 Other means of identification

Product number -
Other names Isopentanethiol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:541-31-1 SDS

541-31-1Relevant articles and documents

Two-step three-component process for one-pot synthesis of 8-alkylmercaptocaffeine derivatives

Rad, M. N. Soltani,Maghsoudi

, p. 70335 - 70342 (2016/08/06)

A highly efficient, odourless and two-step three-component process for one-pot synthesis of some 8-alkylmercaptocaffeine derivatives has been described. The catalyst-free three-component reaction of alkyl bromides, thiourea, and 8-bromocaffeine gave 8-alkylmercaptocaffeine products in excellent to quantitative yields. In addition, the impact of parameters on sample reaction is discussed.

METHOD FOR TREATING ANXIETY WITH MUSCARINIC CHOLINERGIC RECEPTOR AGONISTS

-

, (2008/06/13)

The present invention relates a method for treating anxiety using azacyclic and azabicyclic pyrazine compounds.

Use of azacyclic or azabicyclic pyrazine compounds for treating anxiety

-

, (2008/06/13)

The present invention relates a method for treating anxiety using azacyclic and azabicyclic pyrazine compounds.

Antimicrobial composition and method containing N-(3,5-dihalophenyl)-imide compounds

-

, (2008/06/13)

Novel N-(3,5-dihalophenyl)imide compounds, which exhibit a strong antimicrobial activity against microorganisms including phytopathogenic fungi, parasites of industrial products and pathogenic microorganisms, represented by the formula, STR1 wherein X and X' each represent halogens and A represents a substituted ethylene such as chloroethylene, C1 - C4 alkylthioethylene, C1 - C2 alkyl-ethylene or 1,2-di-C1 - C2 -alkyl-ethylene, a cyclopropylene such as 1,3-dimethylcyclopropylene, trimethylene, a cyclohexylene-1,2-, cyclohexenylene-1,2-, cyclohexadienylene-1,2- or o-phenylene. The N-(3,5-dihalophenyl)imide compounds can be obtained by any of methods which produce imide compounds or reaction of an N-(3,5-dihalophenyl)maleimide compound with a mercaptan, a hydrogen halide, phosphorus chloride or thionylchloride.

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