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473-67-6

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473-67-6 Usage

Description

CIS-VERBENOL, also known as verbenol, is a naturally occurring organic compound found in various plant sources such as spearmint oil, Scotch spearmint oil, juniper berry, myrtle berry, mango, angelica root oil, mastic gum fruit, and leaf oil. It is characterized by its fresh pine and ozone-like odor. CIS-VERBENOL possesses unique chemical properties that make it a versatile compound with a wide range of applications across different industries.

Uses

Used in Fragrance Industry:
CIS-VERBENOL is used as a fragrance ingredient for its fresh pine and ozone-like scent. It is commonly employed in the formulation of perfumes, colognes, and other scented products to provide a refreshing and invigorating aroma.
Used in Flavor Industry:
CIS-VERBENOL is used as a flavoring agent in the food and beverage industry. Its unique scent profile makes it suitable for enhancing the taste of various products, particularly those with a minty or herbal flavor profile.
Used in Aromatherapy:
CIS-VERBENOL is used in aromatherapy for its potential therapeutic benefits. Its refreshing and uplifting scent is believed to help reduce stress, anxiety, and promote relaxation.
Used in Insect Repellent Industry:
CIS-VERBENOL is used as an insect repellent due to its ability to deter certain insects. Its strong odor can help keep insects away, making it a useful component in natural insect repellent products.
Used in Cosmetics Industry:
CIS-VERBENOL is used in the cosmetics industry for its scent and potential skin benefits. It can be found in various cosmetic products such as creams, lotions, and soaps, where it provides a pleasant aroma and may contribute to skin health.
Used in Pharmaceutical Industry:
CIS-VERBENOL has potential applications in the pharmaceutical industry due to its unique chemical properties. It may be used in the development of new drugs or as an active ingredient in various medicinal formulations.

Preparation

Prepared from levo-α-pinene (also written (l)- or (–)-α-pinene). The corresponding dextro-isomer ((d)- or (+)-α-pinene) is not suitable.

Check Digit Verification of cas no

The CAS Registry Mumber 473-67-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 473-67:
(5*4)+(4*7)+(3*3)+(2*6)+(1*7)=76
76 % 10 = 6
So 473-67-6 is a valid CAS Registry Number.
InChI:InChI=1S/C10H16O/c1-6-4-9(11)8-5-7(6)10(8,2)3/h4,7-9,11H,5H2,1-3H3/t7-,8+,9-/m0/s1

473-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name CIS-VERBENOL

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. Food additives -> Flavoring Agents
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:473-67-6 SDS

473-67-6Relevant articles and documents

Individual stereoisomers of verbenol and verbenone express bioactive features

Ivanov, Marija,Kovalenko, Vitaly,Svirid, Anastasia,Kosti?, Marina,Petrovi?, Jovana,Stojkovi?, Dejan

, (2021/12/13)

Naturally occurring terpene core compounds have been used extensively in both pharmaceutical and cosmetic industry. However, since chirality of these compounds has profound influence on the level of their bioactivity, the aim of the present study was to a

Stereospecific synthesis of S-(?)-trans-verbenol and its antipode by inversion of sterically hindered alcohols

Fang, Jia-Xing,Kong, Xiang-Bo,Liu, Fu,Zhang, Su-Fang,Zhang, Zhen

, (2020/12/15)

S-(?)-trans-Verbenol (1) and its antipode, R-(+)-trans-verbenol (1′) have been confirmed as the critical pheromone components of bark beetles. Synthesis of these two active secondary alcohols (1 and 1′) from commercially available starting materials S-α-pinene and R-α-pinene was reported. The key steps were mainly depended on the effective SN2 stereo-inversion of the hydroxy group of sterically hindered alcohols (3 and 3′), using Mitsunobu reaction or hydrolysis of mesylate ester, alternatively. Our results provide a new and stereo-selectivity way to obtain optically active insect pheromones.

Oxy-functionalization of olefins with neat and heterogenized binuclear V(IV)O and Fe(II)complexes: Effect of steric hindrance on product selectivity and output in homogeneous and heterogeneous phase

Parmar, Digvijaysinh K.,Butani, Pinal M.,Thumar, Niraj J.,Jasani, Pinal M.,Padaliya, Ravi V.,Sandhiya, Paba R.,Nakum, Haresh D.,Khan, Md. Nasim,Makwana, Dipak

, (2019/06/05)

Neat {[VO(sal2bz)]2; [Fe(sal2bz)(H2O)2]2·2H2O} and zeolite-Y immobilized {[VO(sal2bz)]2-Y; [Fe(sal2bz)(H2O)2]2-Y} binuclear complexes have been prepared and characterized by spectroscopic techniques (IR, UV–vis), elemental analyses (CHN, ICP-OES), thermal study (TGA), scanning electron micrograph (SEM), adsorption study (BET)and X-ray diffraction (XRD)patterns. Neat (homogeneous)and immobilized (heterogeneous)complexes were employed as catalysts in the oxidation of olefins, namely, cyclohexene, limonene and α-pinene in the presence of 30% hydrogen peroxide. 100% conversion of cyclohexene and α-pinene was obtained while limonene was oxidized up to 90%. Homogeneous catalysts showed highly selective result as neat [VO(sal2bz)]2 complex has provided 87% cyclohexane-1,2-diol and neat [Fe(sal2bz)(H2O)2]2·2H2O complex has provided 79% verbenone in oxidation of cyclohexene and α-pinene, respectively. We have observed that due to steric hindrance, formation of olefinic oxidation products increases on moving from α-pinene to limonene and limonene to cyclohexene. Additionally. recovered heterogeneous catalysts showed intact results up to two consecutive runs. Probable catalytic mechanism has been proposed for oxidation of cyclohexene.

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