1191-08-8 Usage
Description
1,4-Butanedithiol, an alkanedithiol, is a clear colorless to pale yellow liquid that serves as a food odorant. It is known for its distinct smell, which is similar to that of its homologs, such as propane-1,3-dithiol and pentane-1,5-dithiol.
Uses
Used in Food Industry:
1,4-Butanedithiol is used as a flavoring agent for its characteristic odor, which is similar to other alkanedithiols. It is employed to enhance the aroma and taste of various food products, providing a unique and pleasant scent.
Used in Chemical Industry:
1,4-Butanedithiol can be utilized as a building block or intermediate in the synthesis of various organic compounds, particularly those requiring dithiol functional groups. Its chemical properties make it a versatile component in the development of new molecules and materials.
Used in Research and Development:
Due to its unique chemical structure and properties, 1,4-Butanedithiol can be used in research and development for studying the effects of dithiol compounds on various chemical reactions and processes. This can lead to the discovery of new applications and uses for this compound in different industries.
Synthesis Reference(s)
The Journal of Organic Chemistry, 20, p. 50, 1955 DOI: 10.1021/jo01119a009
Check Digit Verification of cas no
The CAS Registry Mumber 1191-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1191-08:
(6*1)+(5*1)+(4*9)+(3*1)+(2*0)+(1*8)=58
58 % 10 = 8
So 1191-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H10S2/c5-3-1-2-4-6/h5-6H,1-4H2
1191-08-8Relevant articles and documents
Eliel et al.
, p. 524 (1975)
3-(2-aminophenyl)-4-methyl-1,3-thiazole-2(3H)-thione as an ecofriendly sulphur transfer agent to prepare alkanethiols in high yield and high purity
Mehdid, Mohammed Amine,Djafri, Ayada,Roussel, Christian,Andreoli, Federico
experimental part, p. 4634 - 4643 (2010/04/06)
A new process is described for preparing very pure linear alkanethiols and linear α,ω-alkanedithiols using a sequential alkylation of the title compound, followed by a ring closure to quantitatively give the corresponding 3-methyl[1,3]thiazolo[3,2-a]-[3,1
A general and mild synthesis of thioesters and thiols from halides
Zheng, Tu-Cai,Burkart, Maureen,Richardson, David E.
, p. 603 - 606 (2007/10/03)
The conversion of a wide variety of halides to thioesters by reaction with potassium thiocetate under mild conditions is described, and the generality of the method is demonstrated.