(S)-2-Aminobutane-1,4-dithiol hydrochloride

99%(titration)

Reagent Code: #237932
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CAS Number 1363376-98-0

science Other reagents with same CAS 1363376-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.73 g/mol
Formula C₄H₁₂NS₂Cl
badge Registry Numbers
MDL Number MFCD23704430
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds for drug manufacturing. Its thiol groups enable conjugation reactions, making it valuable in creating targeted therapeutics and prodrugs. Also employed in asymmetric synthesis due to its chiral amine functionality, supporting the production of enantiomerically pure substances. Additionally, serves as a building block in peptide mimetics and in the design of enzyme inhibitors where sulfur-containing groups are required for activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿35,580.00
(S)-2-Aminobutane-1,4-dithiol hydrochloride
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds for drug manufacturing. Its thiol groups enable conjugation reactions, making it valuable in creating targeted therapeutics and prodrugs. Also employed in asymmetric synthesis due to its chiral amine functionality, supporting the production of enantiomerically pure substances. Additionally, serves as a building block in peptide mimetics and in the design of enzyme inhibitors where sulfur-containing

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral compounds for drug manufacturing. Its thiol groups enable conjugation reactions, making it valuable in creating targeted therapeutics and prodrugs. Also employed in asymmetric synthesis due to its chiral amine functionality, supporting the production of enantiomerically pure substances. Additionally, serves as a building block in peptide mimetics and in the design of enzyme inhibitors where sulfur-containing groups are required for activity.

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