1516-17-2 Usage
Description
TRANS,TRANS-2,4-HEXADIENYL ACETATE is a colorless liquid with a powerful, sweet, pineapple aroma. It has a taste threshold value of 25 ppm in water, which gives it a fresh green, herbal, soapy, and metallic taste. The aroma threshold value of this compound is considered to be of medium strength and falls under the green type category.
Uses
Used in Flavor Industry:
TRANS,TRANS-2,4-HEXADIENYL ACETATE is used as a flavoring agent for its distinctive sweet, pineapple aroma. It is particularly suitable for enhancing the flavor of various food and beverage products, making them more appealing to consumers.
Used in Fragrance Industry:
TRANS,TRANS-2,4-HEXADIENYL ACETATE is used as a fragrance ingredient for its fresh green, herbal, and soapy scent. It can be incorporated into a wide range of personal care and household products, such as perfumes, soaps, and air fresheners, to provide a pleasant and long-lasting aroma.
Used in Aromatherapy:
Due to its medium strength odor and green type aroma, TRANS,TRANS-2,4-HEXADIENYL ACETATE can be used in aromatherapy applications. It may help promote relaxation, stress relief, and a sense of well-being when inhaled or used in massage oils.
Used in Cosmetics Industry:
TRANS,TRANS-2,4-HEXADIENYL ACETATE can be used as a key ingredient in the formulation of cosmetics, such as lotions, creams, and shampoos, for its pleasant aroma and potential benefits to the overall sensory experience of the product.
Safety Profile
Moderately toxic by ingestion andskin contact. A skin and severe eye irritant.
Check Digit Verification of cas no
The CAS Registry Mumber 1516-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1516-17:
(6*1)+(5*5)+(4*1)+(3*6)+(2*1)+(1*7)=62
62 % 10 = 2
So 1516-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-3-4-5-6-7-10-8(2)9/h3-6H,7H2,1-2H3/b4-3+,6-5+
1516-17-2Relevant articles and documents
Highly selective oxidation of allylic alcohols catalysed by monodispersed 8-shell Pd nanoclusters in the presence of molecular oxygen
Choi, Kwang-Min,Akita, Tomoki,Mizugaki, Tomoo,Ebitani, Kohki,Kaneda, Kiyotomi
, p. 324 - 328 (2007/10/03)
Treatment of Pd4phen2(CO)2(OAc)4 with metal nitrates such as Cu(NO3)2 produced monodispersed Pd nanoclusters with a mean diameter and standard deviation (d±σ) of 38±2.1 A (σ/d = 6%). The Pd nanoclusters act as heterogeneous catalysts for the selective oxidation of primary aromatic allylic alcohols using molecular oxygen as an oxidant. This unique catalysis can be ascribed to multiple interactions between the alcohol and specific ensemble sites consisting of Pd0, Pd+, and Pd2+ on the cluster surface.
Stereoselective Synthesis of (2E,4E)- and (2Z,4E)-2,4-Alkadienoates by the Ester Enolate Claisen Rearrangement of (E)-1-Alkyl-3-trimethylsilyl-2-propenyl Glycolates Followed by the Peterson Reaction
Sato, Toshio,Tsunekawa, Hiroshi,Kohama, Hiromasa,Fujisawa, Tamotsu
, p. 1553 - 1556 (2007/10/02)
The ester enolate Claisen rearrangement of (E)-1-alkyl-3-trimethylsilyl-2-propenyl glycolates gave (E)-erythro-2-hydroxy-3-trimethylsilyl-4-alkenoates with high diastereoselectivity, which were stereoselectively converted into (2E,4E)- and (2Z,4E)-2,4-alkadienoates by the Peterson reaction.
