(-)-Borneol TCI B1012

Chemical Identity

CAS No.: 464-45-9
PubChem: CID 439568·SID 87563964
Formula: C10H18O
Molecular weight: 154.25 g/mol
Purity: >95.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
SMILES: CC1(C2CCC1([C@H](C2)O)C)C
InChIKey: DTGKSKDOIYIVQL-ZCUBBSJVSA-N

Rp 928.200,00

~~Rp 664.650,00~~ Rp 928.200,00

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Berat 25g 500g

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(-)-Borneol is an organic compound with a terpenoid structure and serves as one of the enantiomers of borneol. It plays a crucial role in chemical laboratories, particularly in asymmetric synthesis, where it is used as a chiral building block. This compound is essential for the creation of asymmetric molecules, which are vital in various scientific fields. Its chiral nature allows for precise control over stereochemistry in chemical reactions, making it indispensable in advanced synthetic processes.

The physical properties of (-)-Borneol, including its stability and solubility in organic solvents such as ethyl acetate and ethanol, make it a preferred choice for laboratory use. Its characteristic camphor-like aroma also adds to its utility in identifying and handling the compound. The high purity and chiral nature of (-)-Borneol ensure that it meets the stringent requirements of modern chemical synthesis. These attributes contribute to its widespread use in both academic and industrial settings.

In Indonesian laboratories, (-)-Borneol is commonly used in chemical research, especially in higher education institutions and research companies. It is a key component in asymmetric synthesis projects, supporting the development of new pharmaceuticals, organic chemicals, and specialty products. Its availability in crystalline or solid form simplifies handling and integration into laboratory workflows, making it a reliable and essential material for chemists and researchers.

TCI brochures (PDF)

Terpenes 2025-09-22 · p. 5
Chiral Building Blocks 2025-04-14 · p. 10

Related TCI products

Asymmetric synthesis projects benefit from (-)-Borneol's chiral properties, enabling precise control over stereochemical outcomes.
Pharmaceutical research utilizes this compound to develop new drugs with specific stereochemical configurations for enhanced efficacy.
Organic chemistry experiments rely on (-)-Borneol as a chiral building block for constructing complex molecules with defined stereochemistry.
Analytical chemistry applications use (-)-Borneol as a reference standard for chiral separation techniques such as HPLC and GC.
Educational institutions incorporate (-)-Borneol into teaching labs to demonstrate chiral synthesis and stereochemistry concepts.

Brand	TCI
CAS number	464-45-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	—
Physical form	Solid or crystalline
Storage	Store in a cool, dry place away from light

(-)-Borneol should be stored in a cool, dry environment, away from direct light to maintain its stability and purity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended stereochemical changes during synthesis. Proper labeling of containers is essential to ensure safe handling and prevent mix-ups in the laboratory. Always use appropriate personal protective equipment when working with this compound to ensure safety and compliance with laboratory protocols.

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