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61248-45-1

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61248-45-1 Usage

Description

(S)-2-Decen-5-olide, a chemical compound belonging to the class of lactones, is widely recognized for its distinctive fruity, sweet, and creamy odor. This cyclic ester is reminiscent of the delightful scents of coconut, caramel, and peach, making it a popular choice in the fragrance and flavor industry.

Uses

Used in Fragrance Industry:
(S)-2-Decen-5-olide is used as a fragrance ingredient for its ability to impart a fruity, sweet, and creamy aroma to various products. Its pleasant and long-lasting scent enhances the sensory experience, making it a favored choice in perfumes and other fragranced products.
Used in Flavor Industry:
In the flavor industry, (S)-2-Decen-5-olide is used as an additive to provide a natural, fruity, and sweet taste to food products. Its unique flavor profile complements a wide range of culinary applications, contributing to the overall taste and enjoyment of various dishes and beverages.
Used in Cosmetics:
(S)-2-Decen-5-olide is used as a scent enhancer in the cosmetics industry, adding a delightful and long-lasting aroma to products such as body washes and detergents. Its safe and approved status for use in cosmetics ensures that it can be incorporated into a variety of personal care products without causing harm to consumers.
Used in Food Additives:
In the food additives industry, (S)-2-Decen-5-olide is utilized as a flavoring agent to impart a natural, fruity, and sweet taste to a wide range of food products. Its regulatory approval for use in the food industry ensures that it can be safely added to enhance the taste and aroma of various consumables.

Check Digit Verification of cas no

The CAS Registry Mumber 61248-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61248-45:
(7*6)+(6*1)+(5*2)+(4*4)+(3*8)+(2*4)+(1*5)=111
111 % 10 = 1
So 61248-45-1 is a valid CAS Registry Number.

61248-45-1SDS

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 Massoia lactone

1.2 Other means of identification

Product number -
Other names (S)-6-pentyl-5,6-dihydro-2H-pyran-2-one

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:61248-45-1 SDS

61248-45-1Downstream Products

61248-45-1Relevant articles and documents

Preparation method of (R)-(-)-massoialactone

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Paragraph 0055-0058; 0073-0075, (2019/12/25)

The invention discloses a preparation method of (R)-(-)-massoialactone. The preparation method includes the following steps: in a solvent, under the action of a copper salt, an alkali and a ligand, beta,gamma-unsaturated ester and n-hexanal are subjected to a reaction shown in the specification to obtain (R)-(-)-massoalactrone; the copper salt is Cu(CH3CN)4PF6 or the alkali is Barton's Base, alkali metal tert-butanol salt or the ligand is (R,R)-Ph-BPE or (S)-DTBM-SEGPHOS. (R)-(-)-massoialactone can be obtained by one-step reaction with high yield and ee value; compared with other methods in the prior art, the method has many advantages, such as simple route, easy access to raw materials, mild conditions and the like, and has obvious advantages.

Trimethylphosphine-Promoted Alcoholysis of α,β-Unsaturated Imides and α,β-Unsaturated Esters

Sato, Haruka,Hosokawa, Seijiro

, p. 1343 - 1349 (2018/01/27)

α,β-Unsaturated imides and α,β-unsaturated esters were found to undergo alcoholysis in the presence of trimethylphosphine. The reaction is initiated by nucleophilic addition of trimethylphosphine to the double bond of the α,β-unsaturated carbonyl compound. Saturated imides also undergo the alcoholysis in the presence of the corresponding α,β-unsaturated imide.

PPARS AGONIST ACTIVITY ENHANCING DRUG

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Paragraph 0042-0043, (2015/03/03)

According to the present invention, PPARs agonist activity is enhanced in order to improve metabolic syndrome, hyperlipidemia, and diabetes. Provided is a compound having a lactone structure comprising formula (9).

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