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[1R-(1alpha,2beta,5alpha)]-2-isopropenyl-5-methylcyclohexyl isovalerate is a colorless liquid chemical compound with the molecular formula C15H26O2. It is an ester formed by the reaction of an alcohol with an organic acid, characterized by its pleasant, fruity odor. [1R-(1alpha,2beta,5alpha)]-2-isopropenyl-5-methylcyclohexyl isovalerate is categorized as a natural flavoring substance and is generally regarded as safe for use in various applications.

28221-20-7

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28221-20-7 Usage

Uses

Used in Perfume and Flavoring Production:
[1R-(1alpha,2beta,5alpha)]-2-isopropenyl-5-methylcyclohexyl isovalerate is used as a key ingredient in the production of perfumes and flavorings due to its distinctive, fruity scent. Its natural and pleasant aroma makes it a valuable addition to these products.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, [1R-(1alpha,2beta,5alpha)]-2-isopropenyl-5-methylcyclohexyl isovalerate is used as a fragrance component to impart a fresh and appealing scent to products such as lotions, creams, and shampoos. Its natural origin and safety profile contribute to the growing demand for natural ingredients in personal care products.
Used in Household Products:
[1R-(1alpha,2beta,5alpha)]-2-isopropenyl-5-methylcyclohexyl isovalerate is also used as a fragrance in household products like air fresheners and detergents. Its ability to provide a long-lasting and pleasant aroma makes it a popular choice for enhancing the scent of these everyday items.
Used in Food Products:
As a natural flavoring substance, [1R-(1alpha,2beta,5alpha)]-2-isopropenyl-5-methylcyclohexyl isovalerate is used in the food industry to add a fruity note to various food products. Its safety and versatility make it suitable for a wide range of applications, from beverages to confectionery items.

Check Digit Verification of cas no

The CAS Registry Mumber 28221-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,2 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28221-20:
(7*2)+(6*8)+(5*2)+(4*2)+(3*1)+(2*2)+(1*0)=87
87 % 10 = 7
So 28221-20-7 is a valid CAS Registry Number.

28221-20-7SDS

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 L-menthyl isopentanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid, 3-methyl-, 5-methyl-2-(1-methylethyl)cyclohexyl ester, [1R-(1α,2β,5α)]-

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:28221-20-7 SDS

28221-20-7Downstream Products

28221-20-7Relevant academic research and scientific papers

Hydromenthoxycarbonylation of isobutylene in the presence of tetrakis(triphenylphosphine)palladium-based catalyst systems

Suerbaev,Chepaikin,Zhaksylykova

, (2012)

The catalytic activity of the Pd(PPh3)4-TsOH and Pd(PPh3)4-PPh3-TsOH systems in the reaction of isobutylene hydromenthoxycarbonylation with carbon monoxide and l-menthol has been examined. It has been

Hydroxycarbonylation of isobutylene in the presence of the palladium acetylacetonate-triphenylphosphine-p-toluenesulfonic acid catalyst system

Suerbaev,Chepaikin,Zhaksylykova, G. Zh.,Kanybetov,Turkbenov,Abyzbekova

experimental part, p. 206 - 209 (2010/02/28)

The reaction of isobutylene hydroxycarbonylation with carbon monoxide and an alcohol (ethanol, 1-menthol) in the presence of the palladium acetylacetonate-triphenylphosphine-p-toluenesulfonic acid catalytic system was investigated. It was shown that the reaction proceeds regioselectively with the formation of linear products (ethyl isovalerate, 1-menthyl isovalerate). The optimum conditions for running the process were found, at which the yield of the main products is 67-79%.

Method of using a compound of menthol and L-arginine as a preparation for the topical delivery of alprostadil for the treatment of female sexual dysfunction

-

, (2008/06/13)

A manual application of a topical clitoral sensitizing compound combination consisting og L-arginine and a cooling agent comprised of Menthol and aplrostadil, wherein the combination is applicable manually to the clitoris

Topical menthol, or a related cooling compound, to induce lubrication

-

, (2008/06/13)

Vaginal Lubrication is an important component of a woman's sexual arousal. The other components are vaginal vasocongestion and the establishment of a clitoral erection. The use of menthol or any related cooling compound, topically applied to the clitoris, evokes a reflex vaginal lubrication, via the clitoral nociceptors, the spinal autonomic nerves, and inducing the reflex release of vasoactivepolypeptides adjacent to the vaginal arterioles. The vaginal lubrication can be an effective therapy for atrophic vaginitis, the most common cause of dyspareunia (pain with intercourse).

Methods to treat one or all of the defined etiologies of female sexual dysfunction

-

, (2008/06/13)

The U.S. Food and Drug Administration defines the four separate components of Female Sexual Dysfunction (FSD) to be decreased sexual desire, decreased sexual arousal, dyspareunia (pain with intercourse), and persistent difficulty in achieving or inability to achieve orgasm (anorgasmia). To establish a diagnosis of FSD, these components must be associated with personal distress, as determined by the affected woman. A topical combination of menthol/L-arginine and the specific 5-PDE inhibitor vardenafil can be used to treat any of the defined components, or a combination of two or more of the defined components of FSD, as a safe, first-line therapy for FSD.

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