1115-11-3 Usage
Description
Tiglic aldehyde, also known as 2-Methyl-2-butenal, is a volatile organic compound characterized by its colorless to light yellow clear liquid appearance and a strong, pleasant, fruity odor. It is synthesized from perillaldehyde and is recognized for its sharp, citrusy scent, making it a popular choice in the cosmetic, food, and perfume industries as a fragrance and flavoring agent. However, it is important to note that it can be a skin, eye, and respiratory tract irritant, with potential for causing allergic skin reactions upon prolonged exposure. Its chemical formula is C5H8O.
Uses
Used in the Cosmetic Industry:
Tiglic aldehyde is used as a fragrance ingredient in the cosmetic industry for its ability to impart a sharp, citrusy scent to various products, enhancing their appeal to consumers.
Used in the Food Industry:
In the food industry, Tiglic aldehyde serves as a flavoring agent, adding a distinctive citrus flavor to food products, thereby improving their taste and consumer experience.
Used in the Perfume Industry:
Tiglic aldehyde is utilized as a key component in perfumery, where its strong, pleasant, fruity odor contributes to the creation of various fragrances, providing a unique and attractive scent profile.
It is crucial to handle Tiglic aldehyde with care due to its potential irritant properties, ensuring that it is used in appropriate concentrations and within safe exposure limits to minimize the risk of adverse effects on skin, eyes, and the respiratory tract.
Check Digit Verification of cas no
The CAS Registry Mumber 1115-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1115-11:
(6*1)+(5*1)+(4*1)+(3*5)+(2*1)+(1*1)=33
33 % 10 = 3
So 1115-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O/c1-3-5(2)4-6/h3-4H,1-2H3/b5-3+
1115-11-3Relevant articles and documents
Doebner,Luecker
, p. 590 (1896)
The bioinspired design of a reagent allows the functionalization of Cα-H of α,β-unsaturated carbonyl compounds via the Baylis-Hillman chemistry under ambient conditions
Singh, Palwinder,Kumar, Arun,Kaur, Sukhmeet,Kaur, Jagroop,Singh, Harpreet
supporting information, p. 2936 - 2939 (2016/02/20)
A rationally designed reagent capable of affecting alkylation at Cα of α,β-unsaturated carbonyl compounds is reported. The reaction proceeded at room temperature without any additives. The pH and H-bond formation during the reaction play a key role in the working of the reagent.
BIOMIMETIC SYNTHESIS OF BACTERIAL C50 CAROTENOIDS DECAPRENOXANTHIN AND C.p. 450
Ferezou, Jean-Pierre,Julia, Marc
, p. 1277 - 1288 (2007/10/02)
Alkylation of the distal double bond of pseudoionone 4 has been carried out with isoprene epoxide (ZnCl2/MeNO2) leading directly to α-cis 10a, α-trans 10b and γ 10c hydroxyprenylionones.The α-cis and γ-isomers have been converted in few steps into the C50 carotenoids decaprenoxanthin 1 and C.p. 450 3 respectively.
