2721-22-4 Usage
Uses
Used in Flavor and Fragrance Industry:
delta-Tetradecalactone is used as a flavoring agent for its distinct buttery, fatty, and creamy taste. It is particularly suitable for enhancing the flavor profiles of dairy products, baked goods, and confectioneries.
Used in the Food Industry:
delta-Tetradecalactone is used as an additive in the food industry to impart a rich, creamy, and buttery flavor to various products. Its natural occurrence in several food items makes it a preferred choice for achieving authentic taste characteristics.
Used in the Cosmetic Industry:
Due to its creamy and buttery aroma, delta-Tetradecalactone can be used as a fragrance component in the cosmetic industry, particularly in products that aim to evoke a luxurious and indulgent sensory experience.
Used in the Perfumery:
The unique aroma of delta-Tetradecalactone makes it a valuable ingredient in the creation of perfumes, where it can contribute to a rich, creamy, and comforting scent profile.
Used in the Aromatherapy Industry:
The buttery and creamy characteristics of delta-Tetradecalactone can be utilized in aromatherapy for creating soothing and comforting blends that promote relaxation and a sense of well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 2721-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2721-22:
(6*2)+(5*7)+(4*2)+(3*1)+(2*2)+(1*2)=64
64 % 10 = 4
So 2721-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O2/c1-2-3-4-5-6-7-8-10-13-11-9-12-14(15)16-13/h13H,2-12H2,1H3
2721-22-4Relevant academic research and scientific papers
Synthesis, antibacterial activities, and sustained perfume release properties of optically active5-hydroxy- And 5-acetoxyalkanethioamide analogues
Shimotori, Yasutaka,Hoshi, Masayuki,Ogawa, Narihito,Miyakoshi, Tetsuo,Kanamoto, Taisei
, p. 84 - 98 (2020/07/03)
5-Acetoxy- and 5-hydroxyalkanethioamide analogues showed high antibacterial activity against Staphylococcus aureus. Antibacterial thioamides were prepared from 5-alkyl-δ-lactones by amidation, thionation, and subsequent deacetylation. Optically active thioamides with 99% diastereomeric excesses were prepared by diastereomeric resolution using Cbz-L-proline as the resolving agent. Antibacterial thioamides were slowly lactonized by a lipase catalyst. Therefore, these thioamides are potential sustained-release perfume compounds having antibacterial properties.
Catalytic oxidation of alkyl- and cycloalkylcyclanones into lactones
Abbasov,Alimardanov,Suleimanova
, p. 621 - 626 (2007/10/03)
Pilot-plant syntheses of alkyl and cycloalkylcyclanones and their subsequent liquid-phase oxidation into lactones are described. Characteristics of resulting intermediates and target products are reported.
