4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol
[CAS# 131538-00-6]

Identification

• Classification: Chemical reagent >> Organic reagent >> Thiol/thiophenol
• Name: 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol
• Synonyms: 1,2-Bis[(2-mercaptoethyl)thio]-3-mercaptopropane; 2,3-Bis[(2-mercaptoethyl)thio]-1-propanethiol; 4-(Mercaptomethyl)-1,8-dimercapto-3,6-dithiaoctane
• Molecular Formula: C₇H₁₆S₅
• Molecular Weight: 260.53
• CAS Registry Number: 131538-00-6
• EC Number: 411-290-7
• SMILES: C(CSCC(CS)SCCS)S

Properties

• Density: 1.2±0.1 g/cm³, Calc.^*
• Index of Refraction: 1.607, Calc.^*
• Boiling Point: 395.6±42.0 ºC (760 mmHg), Calc.^*
• Flash Point: 193.0±27.9 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS08;GHS07;GHS09 Warning
• Hazard Statements: H302-H373-H400-H410
• Precautionary Statements: P203-P260-P261-P264-P270-P272-P273-P280-P301+P317-P302+P352-P308+P316-P318-P319-P321-P330-P333+P317-P362+P364-P391-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Chronic hazardous to the aquatic environment	Aquatic Chronic	1	H410
Acute hazardous to the aquatic environment	Aquatic Acute	1	H400
Specific target organ toxicity - repeated exposure	STOT RE	2	H373
Acute toxicity	Acute Tox.	4	H302
Reproductive toxicity	Repr.	2	H361
Skin sensitization	Skin Sens.	1	H317
Specific target organ toxicity - single exposure	STOT SE	2	H371

• Transport Information: UN 3335

Discovory and Applicatios

4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol, commonly known as a specialized dithiol compound, is an organosulfur chemical with notable applications in various industrial and chemical processes. This compound features a unique structure with multiple thiol (sulfhydryl) groups, which impart it with significant reactivity and functionality.

The discovery of 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol arose from the study of organosulfur compounds and their potential applications in materials science and catalysis. The compound's synthesis typically involves the reaction of appropriate thiol and disulfide precursors under controlled conditions to form the dithiol structure. The presence of multiple thiol groups enhances its ability to interact with other chemical species, making it a valuable component in several specialized applications.

One of the primary applications of 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol is in the field of polymer chemistry. The compound is used as a crosslinking agent in the synthesis of polymers and elastomers. Its multiple thiol groups facilitate the formation of strong crosslinks between polymer chains, which improves the mechanical properties and stability of the resulting materials. This property is particularly useful in the production of high-performance rubber and elastomeric compounds used in various industrial applications.

In addition to its role in polymer chemistry, 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol is utilized as a stabilizer in the formulation of certain metal and semiconductor materials. The compound’s thiol groups can form strong bonds with metal surfaces, providing protective layers that prevent oxidation and degradation. This application is crucial in maintaining the performance and longevity of electronic components and metal-based products.

The compound also finds use in the field of catalysis, where it serves as a ligand in metal-catalyzed reactions. The thiol groups in 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol can coordinate with metal centers, influencing the reactivity and selectivity of catalytic processes. This makes it a valuable tool in the development of novel catalytic systems for various chemical transformations.

Despite its advantageous properties, the handling of 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol requires careful attention to safety due to the reactivity of its thiol groups. Proper safety protocols must be followed during its synthesis and application to mitigate any potential risks associated with its use.

Overall, 4-(Mercaptomethyl)-3,6-dithia-1,8-octanedithiol is a versatile compound with significant applications in polymer chemistry, material stabilization, and catalysis. Its unique chemical structure and reactivity make it an important component in various industrial and research settings.