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[1S-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl acetate, commonly known as bornyl acetate, is a bicyclic terpene derivative that is naturally found in essential oils such as pine, fir, and cypress. It is characterized by its pleasant, fresh, and woody aroma, making it a popular choice for various applications.

39776-80-2

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39776-80-2 Usage

Uses

Used in Fragrance and Flavor Industry:
Bornyl acetate is used as a key ingredient in the fragrance and flavor industry due to its fresh, woody, and pleasant aroma. It is commonly found in perfumes, air fresheners, and household cleaning products, adding a distinct and appealing scent to these products.
Used in Aromatherapy:
In aromatherapy, bornyl acetate is utilized for its calming and relaxing effects. Its soothing properties make it a popular choice for creating a tranquil and peaceful atmosphere, which can help reduce stress and anxiety.
Used in Antimicrobial Applications:
Bornyl acetate is being studied for its potential antimicrobial properties, which could make it useful in the development of new treatments for various infections and diseases.
Used in Anti-inflammatory Applications:
[1S-(1alpha,2beta,3alpha,5alpha)]-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl acetate is also being investigated for its anti-inflammatory effects, which could lead to its use in the development of medications for conditions characterized by inflammation.
Used in Antioxidant Applications:
Additionally, bornyl acetate is being researched for its antioxidant properties, which may contribute to its potential use in the development of products that promote overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 39776-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,7 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39776-80:
(7*3)+(6*9)+(5*7)+(4*7)+(3*6)+(2*8)+(1*0)=172
172 % 10 = 2
So 39776-80-2 is a valid CAS Registry Number.

39776-80-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6,6-Trimethylbicyclo[3.1.1]hept-3-yl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:39776-80-2 SDS

39776-80-2Downstream Products

39776-80-2Relevant academic research and scientific papers

Chemically synthesized and cross-linked PDMS as versatile alignment medium for organic compounds

Moskalenko, Yulia E.,Bagutski, Viktor,Thiele, Christina M.

supporting information, p. 95 - 98 (2016/12/27)

A useful procedure for the preparation of chemically synthesized and cross-linked polydimethylsiloxane (PDMS) gels is presented, which does not require β-irradiation for cross-linking. NMR spectra of high quality are obtained, such that even mixtures of compounds exhibiting similar NMR spectra like interconverting stereoisomers can be investigated in the residual dipolar coupling (RDC) approach of organic structure determination.

ENANTIOSELECTIVITY IN THE HYDROLYSIS OF BICYCLIC MONOTERPENE ACETATES WITH THE CULTURED CELLS OF NICOTIANA TABACUM

Suga, Takayuki,Hirata, Toshifumi,Izumi, Shunsuke

, p. 2791 - 2792 (2007/10/02)

Key Word Index - Nicotiana tabacum; Solanaceae; tissue culture; biotransformation; hydrolysis; enantioselectivity; bicyclic monoterpene acetates.The enantioselectivity in the hydrolysis of bornyl acetate; isobornyl acetate and isopinocampheyl acetate with the cultured cells of Nicotiana tabacum was investigated.The cultured cells were found to have the ability to hydrolyse enantioselectively the acetates, of which the configuration at the carbon atom bearing the acetoxyl group is R.

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