CAS 76-49-3

(±)-Bornyl acetate

Description:

(±)-Bornyl acetate is an organic compound classified as an ester, specifically derived from bornyl alcohol and acetic acid. It is a colorless to pale yellow liquid with a characteristic pleasant, pine-like aroma, making it popular in the fragrance and flavor industries. The compound has a relatively low boiling point and is soluble in organic solvents, but only slightly soluble in water. Its molecular formula is C12H20O2, and it features a bicyclic structure typical of terpenes, which contributes to its distinctive scent. (±)-Bornyl acetate is often used in perfumes, cosmetics, and food flavorings due to its aromatic properties. Additionally, it exhibits some antimicrobial and insect-repellent activities, making it of interest in various applications beyond fragrance. As a chiral compound, it exists in two enantiomeric forms, but the racemic mixture is commonly referred to as (±)-Bornyl acetate. Safety data indicates that it should be handled with care, as it can cause irritation upon contact with skin or eyes.

Formula: C₁₂H₂₀O₂

InChI: InChI=1/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10+,12+/s2

InChI key: InChIKey=KGEKLUUHTZCSIP-QJUVKGSQNA-N

SMILES: C[C@@]12[C@H](OC(C)=O)C[C@@](C1(C)C)(CC2)[H]

Synonyms:

• 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-ol acetate
• 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-yl acetate, endo-
• 2-Camphanol acetate
• 2-Camphanyl acetate
• Acetate de endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yle
• Acetate, 1,7,7-Trimethyl-Bicyclo(2.2.1)Hept-2-Yl, Endo-
• Acetato De Endo-1,7,7-Trimetilbiciclo[2.2.1]Hept-2-Ilo
• Ai3-00665
• Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, 2-acetate, (1R,2S,4R)-rel-
• Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, acetate, (1R,2S,4R)-rel-
• Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, acetate, endo-
• Borneol, acetate
• Borneol, acetate (8CI)
• Borneyl acetate
• Bornyl acetic ester
• Bornyl acetic ether
• Bornyl ethanoate
• Endo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl aceatate
• FEMA No. 2159
• Nsc 407158
• dl-Bornyl acetate
• endo-1,7,7-Trimethylbicyclo(2.2.1)hept-2-yl acetate
• endo-1,7,7-Trimethylbicyclo[2.2.1]hept-2-ylacetat
• endo-2-Camphanyl ethanoate
• endo-Bornyl acetate

Bicyclo[2.2.1]heptan-2-ol,1,7,7-trimethyl-, 2-acetate, (1R,2S,4R)-rel-

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Purity: 97%

Molecular weight: 196.2860

Ref: IN-DA0038GL

Bornyl acetate

CAS: 76-49-3

Bornyl acetate

Purity: ≥98%

Molecular weight: 196.29g/mol

Ref: 54-BUP14902

Bornyl acetate

CAS: 76-49-3

Bornyl acetate (Isobornyl acetate) has an anti-inflammatory effect. It is the volatile ingredient in some Chinese traditional herbs and numerous conifer oils.

Formula: C₁₂H₂₀O₂

Purity: 99.19%

Color and Shape: Liquid

Molecular weight: 196.29

Ref: TM-T1246

Bornyl Acetate

CAS: 76-49-3

Bornyl Acetate

Purity: 97%,mixtures

Molecular weight: 196.29g/mol

Ref: 54-OR1030105

Bornyl Acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Color and Shape: Colorless Liquid

Molecular weight: 196.29

Ref: 4Z-B-145001

Bornyl acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Purity: 95%~99%

Molecular weight: 196.29

Ref: BP-BP0280

Bornyl acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Purity: ≥ 90.0%

Color and Shape: Clear, colourless to pale yellow liquid

Molecular weight: 196.29

Ref: 7W-GY0324

Bornyl Acetate (Mixture of Diastereomers)

CAS: 76-49-3

Applications Bornyl Acetate (Mixture of Diastereomers) is a monoterpene ester, and also the main, natural constituent of valerian root oil. Bornyl acetate also has analgesic and anti-inflammatory properties.
References Buchbauer, G., et al.: Die Pharm., 47, 620 (1992); Oh, H., et al.: Appl. Micro., 15, 777 (1967); Wu, X., et al.: J. Chinese Med. Mat., 27, 438 (2004)

Formula: C₁₂H₂₀O₂

Color and Shape: Neat

Molecular weight: 196.29

Ref: TR-B675555

Bornyl Acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Molecular weight: 196.29

Ref: ST-EA-CP-B454000

(+/-)-Bornyl acetate

CAS: 76-49-3

(-)Bornyl acetate is a natural product that has been shown to have antimicrobial properties. It is extracted from plants such as the Boronia and has been shown to inhibit the growth of bacteria. (-)Bornyl acetate interacts with hydroxyl groups on proteins, inhibiting their function. This interaction leads to the production of reactive oxygen species, which causes cellular damage and death. Bornyl acetate also can interact with other sites on proteins, including the nitro group, which may lead to reduced nitric oxide production and decreased inflammatory response. The compound class of (-)bornyl acetate includes alkanoic acids and fatty acids. Molecular docking analysis has identified a number of possible binding sites for this molecule in protein structures. -Bornyl acetate is not active against viruses or fungi.br>br> Bornyl acetate has been shown to be an anti-inflammatory agent that inhibits prostaglandin synthesis and exhibits anti-infective properties.br>br

Formula: C₁₂H₂₀O₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 196.29 g/mol

Ref: 3D-FB74112