(S)-(+)-1,3-Butanediol TCI B1160

Chemical Identity

CAS No.: 24621-61-2
PubChem: CID 446973·SID 87564100
Formula: C4H10O2
Molecular weight: 90.12 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3S)-butane-1,3-diol
SMILES: C[C@@H](CCO)O
InChIKey: PUPZLCDOIYMWBV-BYPYZUCNSA-N

Rp 848.400,00

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(S)-(+)-1,3-Butanediol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific optical configurations. As a key component in chiral building blocks, it plays a vital role in organic chemistry and pharmaceutical research. This compound is essential for creating complex molecules with defined stereochemistry, which is critical in drug development and advanced chemical synthesis. Its unique optical activity makes it a preferred choice for laboratories aiming to achieve precise molecular structures.

The compound’s stable chemical properties and predictable behavior in various reaction conditions make it highly reliable for synthetic processes. Its ability to act as a precursor for molecules with specific configurations enhances its utility in asymmetric catalysis and stereoselective reactions. The clear optical activity of (S)-(+)-1,3-Butanediol ensures that it can be used effectively in controlled synthesis environments, contributing to the accuracy and reproducibility of laboratory results.

In Indonesian laboratories, (S)-(+)-1,3-Butanediol is commonly used in both academic and industrial research settings. It supports the development of new compounds with potential applications in medicine, materials science, and chemical engineering. Researchers in pharmaceutical and chemical industries rely on this compound for its role in creating chiral molecules with specific biological activities. Its availability and performance make it a standard reagent in many laboratory workflows.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 16

Related TCI products

Asymmetric synthesis for the production of chiral compounds with specific optical activity.
Pharmaceutical research to develop drugs with enhanced stereochemical specificity and efficacy.
Organic chemistry experiments requiring precise stereochemical control in reaction pathways.
Material science applications for the synthesis of chiral polymers and advanced functional materials.
Academic research in chemical education and training for students studying stereochemistry and synthesis techniques.

Brand	TCI
CAS number	24621-61-2
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per standard chemical supply practices
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

(S)-(+)-1,3-Butanediol should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a tightly sealed container to avoid exposure to moisture and air. Due to its chemical nature, it should be stored away from incompatible substances such as strong oxidizers or acids. Proper ventilation is essential when handling the compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when working with this material. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in research and synthesis applications.

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