7774-65-4 Usage
Description
Terpinyl isobutyrate is an organic compound with a fruity, floral, and herbaceous odor, along with a heavy, fruity-type flavor. It is commonly used as a flavoring agent and fragrance component in various industries.
Uses
Used in Flavor and Fragrance Industry:
Terpinyl isobutyrate is used as a flavoring agent for its fruity and floral taste, adding a pleasant aroma to food products and beverages.
Terpinyl isobutyrate is also used as a fragrance component in perfumes, soaps, and other personal care products, providing a refreshing and natural scent.
Used in Aromatherapy:
Due to its pleasant and soothing scent, Terpinyl isobutyrate is used in aromatherapy to promote relaxation and stress relief.
Used in Cosmetics:
Terpinyl isobutyrate is used in cosmetics as a fragrance ingredient, enhancing the sensory experience of skincare and beauty products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Terpinyl isobutyrate is used as a flavoring agent in medications to improve their taste and make them more palatable for patients.
Preparation
By esterification of terpineol with isobutyric acid
Check Digit Verification of cas no
The CAS Registry Mumber 7774-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7774-65:
(6*7)+(5*7)+(4*7)+(3*4)+(2*6)+(1*5)=134
134 % 10 = 4
So 7774-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H24O2/c1-10(2)13(15)16-14(4,5)12-8-6-11(3)7-9-12/h6,10,12H,7-9H2,1-5H3
7774-65-4Relevant articles and documents
Discovery of a novel series of α-terpineol derivatives as promising anti-asthmatic agents: Their design, synthesis, and biological evaluation
Zhu, Wanping,Liu, Xia,Wang, Yuji,Tong, Yeling,Hu, Yongzhou
, p. 419 - 425 (2017/12/07)
A series of novel α-terpineol derivatives were designed and synthesized through structural derivatization of the tertiary hydroxyl moiety or reduction of the double bond. Of the resulting compounds, eight compounds enhanced relaxation of airway smooth muscle (ASM) compared to the α-terpineol precursor, and four compounds (4a, 4d, 4e, and 4i)were superior or comparable to aminophylline at a concentration of 0.75 mmol/L. Assays for 3′-5′-Cyclic adenosine monophpsphate (cAMP) activation revealed that some representative α-terpineol derivatives in this series were capable of upregulating the level of cAMP in ASM cells. Further in vivo investigation using the asthmatic rat model, illustrated that treatment with the compounds 4a and 4e resulted in significantly lowered lung resistance (RL) and enhanced dynamic lung compliance (Cldyn), two important parameters for lung fuction. Moreover, treatment with 4e downregulated the levels of both IL-4 and IL-17. Due to its several favorable physiological functions, including ASM relaxation activity, cAMP activation capability, and in vivo anti-asthmatic efficacy, 4e is a promising remedy for bronchial asthma, meriting extensive development.