CAS 76-49-3

(±)-Acetato di bornile

Descrizione:

(±)-Acetato di bornile è un composto organico classificato come un estere, specificamente derivato dall'alcol bornilico e dall'acido acetico. È un liquido incolore o giallo pallido con un aroma caratteristico piacevole, simile al pino, che lo rende popolare nelle industrie delle fragranze e dei sapori. Il composto ha un punto di ebollizione relativamente basso ed è solubile in solventi organici, ma solo leggermente solubile in acqua. La sua formula molecolare è C12H20O2 e presenta una struttura biciclica tipica dei terpeni, che contribuisce al suo profumo distintivo. (±)-Acetato di bornile è spesso utilizzato in profumi, cosmetici e aromatizzanti alimentari grazie alle sue proprietà aromatiche. Inoltre, mostra alcune attività antimicrobiche e repellenti per insetti, rendendolo interessante in varie applicazioni oltre alla fragranza. Come composto chirale, esiste in due forme enantiomeriche, ma la miscela racemica è comunemente chiamata (±)-Acetato di bornile. I dati di sicurezza indicano che deve essere maneggiato con cura, poiché può causare irritazione al contatto con la pelle o gli occhi.

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]

Sinonimi:

• 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

Purezza: 97%

Peso molecolare: 196.2860

Ref: IN-DA0038GL

Bornyl acetate

CAS: 76-49-3

Bornyl acetate

Purezza: ≥98%

Peso molecolare: 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

Purezza: 99.19%

Colore e forma: Liquid

Peso molecolare: 196.29

Ref: TM-T1246

Bornyl Acetate

CAS: 76-49-3

Bornyl Acetate

Purezza: 97%,mixtures

Peso molecolare: 196.29g/mol

Ref: 54-OR1030105

Bornyl Acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Colore e forma: Colorless Liquid

Peso molecolare: 196.29

Ref: 4Z-B-145001

Bornyl acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Purezza: 95%~99%

Peso molecolare: 196.29

Ref: BP-BP0280

Bornyl acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Purezza: ≥ 90.0%

Colore e forma: Clear, colourless to pale yellow liquid

Peso molecolare: 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

Colore e forma: Neat

Peso molecolare: 196.29

Ref: TR-B675555

Bornyl Acetate

CAS: 76-49-3

Formula: C₁₂H₂₀O₂

Peso molecolare: 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

Purezza: Min. 95%

Colore e forma: Clear Liquid

Peso molecolare: 196.29 g/mol

Ref: 3D-FB74112