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1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol is a complex terpene alcohol compound characterized by its strong, woody, and musky odor. It is commonly found in the essential oils of various plants and is known for its antimicrobial properties, making it a versatile compound with applications in multiple industries.

86747-08-2

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  • 1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol

    Cas No: 86747-08-2

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86747-08-2 Usage

Uses

Used in Perfume and Fragrance Industry:
1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol is used as a fragrance ingredient for its distinctive woody and musky scent, contributing to the creation of long-lasting and complex perfumes and fragrances.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol is utilized as an antimicrobial agent, leveraging its natural ability to combat microorganisms and potentially contributing to the development of new treatments and medications.
Used in Cosmetic Industry:
1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol is employed as a preservative and antimicrobial agent in cosmetics, ensuring the safety and longevity of cosmetic products while maintaining their quality.
Used as a Flavoring Agent in Food Industry:
1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol is used in the food industry as a flavoring agent, adding depth and complexity to various food products, enhancing their taste profiles.
Used in Insect Repellent Industry:
1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol is incorporated into insect repellents due to its natural properties that deter insects, providing an effective and eco-friendly alternative to synthetic repellents.
The diverse applications of 1,2,3,5,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2α-naphthalenemethanol highlight its importance and value across a range of consumer and industrial products, from enhancing sensory experiences to contributing to health and hygiene.

Check Digit Verification of cas no

The CAS Registry Mumber 86747-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,4 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86747-08:
(7*8)+(6*6)+(5*7)+(4*4)+(3*7)+(2*0)+(1*8)=172
172 % 10 = 2
So 86747-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-11-6-5-7-12-8-9-13(14(2,3)16)10-15(11,12)4/h8,11,13,16H,5-7,9-10H2,1-4H3/t11-,13-,15+/m1/s1

86747-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2R,8R,8aS)-8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl]propan-2-ol

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:86747-08-2 SDS

86747-08-2Upstream product

86747-08-2Relevant articles and documents

FRAGRANT SESQUITERPENES FROM AGARWOOD

Ishihara, Masakazu,Tsuneya, Tomoyuki,Uneyama, Kenji

, p. 1147 - 1156 (2007/10/02)

Two new sesquiterpene aldehydes, (-)-selina-3,11-dien-14-al and (+)-selina-4,11-dien-14-al, methyl ester derivatives of three new sesquiterpene carboxylic acids, (-)-methyl selina-3,11-dien-14-oate, (+)-methyl selina-4,11-dien-14-oate, and (+)-methyl 9-hydroxyselina-4,11-dien-14-oate, and a new nor-sesquiterpene ketone, (+)-1,5-epoxy-nor-ketoguaiene, have been isolated from Aquilaria agallocha (agarwood).Their structures have been established on the basis of detailed spectroscopic analyses and synthesis.The occurrences of dehydrojinkoh-eremol and neopetasane in agarwood were also confirmed by comparison of their mass spectral data and Rt on capillary GC with those of synthesized samples.The odoriferous properties of some natural and synthesized sesquiterpenes are also described. Key Word Index: Aquilaria agallocha; Thymelaeceae; agarwood; sesquiterpenes; (-)-selina-3,11-dien-14-al; (+)-selina-4,11-dien-14-al; selina-3,11-dien-14-oic acid; selina-4,11-dien-14-oic acid; 9-hydroxyselina-4,11-dien-14-oic acid; (+)-1,5-epoxy-nor-ketoguaiene; dehydrojinkoh-eremol; neopetasane.

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