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D-(+)-Camphor

Category:,
CAS No.:464-49-3
Product Grade: Industrial Grade
Purity / Assay: ≥98.0%
Molecular Formula:C₁₀H₁₆O
Molecular Weight:152.23 g/mol
EINECS No.:207-355-2
Synonym(s):D-CAMPHOR; (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one; (R)-(+)-Camphor; (R)-Camphor
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D-(+)-Camphor, identified by CAS 464-49-3, is a naturally occurring bicyclic monoterpene ketone characterized by its distinct, penetrating aroma and waxy, crystalline appearance. As a dextrorotatory isomer, it is primarily derived from the wood of the camphor laurel tree or synthesized from pinene. It possesses unique physical properties, including the ability to sublime at room temperature and high solubility in organic solvents, making it a versatile component in various chemical formulations.

In industrial and research settings, this compound is valued for its specific chirality and chemical reactivity. It serves as a foundational building block in organic synthesis and as a chiral auxiliary in asymmetric reactions. Due to its volatility and characteristic scent, it requires careful handling and storage in tightly sealed containers away from heat sources. Its multifaceted nature ensures its continued relevance across the fragrance, polymer, and specialty chemical sectors.

• In the field of organic synthesis, D-(+)-Camphor is utilized as a vital chiral starting material and auxiliary. Researchers leverage its rigid bicyclic structure to induce stereoselectivity in complex chemical reactions, facilitating the production of enantiopure intermediates for specialty chemicals and advanced materials.

• Within the polymer and coatings industry, this compound functions as an effective plasticizer, particularly for nitrocellulose and other cellulose esters. It helps improve the flexibility and durability of films and lacquers, while also acting as a stabilizer to prevent the degradation of certain resinous formulations over time.

• The fragrance and cosmetic industries employ D-(+)-Camphor for its cooling sensation and aromatic profile. It is frequently incorporated into topical formulations, liniments, and personal care products where its volatile nature provides a refreshing effect, and it also serves as a traditional preservative or moth repellent in domestic and industrial storage applications.

25kg/drum, 180kg/drum, IBC Drum
CAS No.: 464-49-3

Product Name: D-(+)-Camphor

Purity / Assay:≥98.0%
Molecular Formula:C₁₀H₁₆O
Molecular Weight:152.23 g/mol
EINECS No.:207-355-2
Synonym(s):D-CAMPHOR; (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one; (R)-(+)-Camphor; (R)-Camphor

D-(+)-Camphor, identified by CAS 464-49-3, is a naturally occurring bicyclic monoterpene ketone characterized by its distinct, penetrating aroma and waxy, crystalline appearance. As a dextrorotatory isomer, it is primarily derived from the wood of the camphor laurel tree or synthesized from pinene. It possesses unique physical properties, including the ability to sublime at room temperature and high solubility in organic solvents, making it a versatile component in various chemical formulations.

In industrial and research settings, this compound is valued for its specific chirality and chemical reactivity. It serves as a foundational building block in organic synthesis and as a chiral auxiliary in asymmetric reactions. Due to its volatility and characteristic scent, it requires careful handling and storage in tightly sealed containers away from heat sources. Its multifaceted nature ensures its continued relevance across the fragrance, polymer, and specialty chemical sectors.

For global customers, we provide complete technical documentation to support product evaluation, regulatory compliance and safe handling during transportation and application.

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