(R)-1,2-Butanediol TCI B4118

Chemical Identity

CAS No.: 40348-66-1
PubChem: CID 641012·SID 253659633
Formula: C4H10O2
Molecular weight: 90.12 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-butane-1,2-diol
SMILES: CC[C@H](CO)O
InChIKey: BMRWNKZVCUKKSR-SCSAIBSYSA-N

Rp 848.400,00

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(R)-1,2-Butanediol is a chiral compound widely used in asymmetric synthesis to construct molecules with optical activity. This material plays a crucial role in laboratories where precise control over stereochemistry is required. Its application spans various fields, including pharmaceutical research, organic chemistry, and the development of bioactive compounds. As a chiral building block, it enables the synthesis of complex molecules with specific stereochemical configurations, which are essential in drug development and advanced chemical research.

The compound's stability and reactivity make it a preferred choice for researchers working on asymmetric reactions. Its R configuration distinguishes it from the S isomer, allowing for the selective formation of desired enantiomers. This property is vital in creating compounds with specific biological activities, such as pharmaceuticals and agrochemicals. The compound's ability to participate in a wide range of chemical transformations further enhances its utility in synthetic chemistry.

In Indonesian laboratories, (R)-1,2-Butanediol is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of pharmacologically active compounds. It is a key reagent in studies focused on the synthesis of new compounds with defined stereochemistry. Its application is also seen in academic and industrial research settings where chiral intermediates are needed for further chemical transformations.

TCI brochures (PDF)

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

Related TCI products

Asymmetric synthesis in pharmaceutical research due to its chiral configuration and ability to control stereochemistry
Organic chemistry experiments requiring precise stereochemical control for the synthesis of optically active compounds
Development of bioactive compounds in medicinal chemistry where enantiomeric purity is essential
Research into chiral intermediates for the production of pharmaceuticals and agrochemicals
Academic studies focused on the synthesis of complex molecules with defined stereochemical configurations

Brand	TCI
CAS number	40348-66-1
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from light

(R)-1,2-Butanediol should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent evaporation and contamination. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. Avoid contact with incompatible materials, and ensure that spill containment measures are in place. Regular monitoring of storage conditions is advised to maintain the compound's integrity and ensure safe laboratory practices.

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