3572-06-3 Usage
Description
4-(4-Acetoxyphenyl)-2-butanone, also known as 4-(3-Oxobutyl)phenyl acetate, is a yellow liquid with a sweet, raspberry, and fruity odor. It is a standard melon fly attractant and is also used as a pheromone for sexual attraction in insects.
Uses
Used in Insect Detection and Control:
4-(4-Acetoxyphenyl)-2-butanone is used as an attractant for detection programs aimed at melon fly and other cuelure-responding Bactrocera fruit flies. It serves as a pheromone to lure these insects into traps, aiding in their detection and control.
Used in Melon Fly Traps:
In the agricultural industry, 4-(4-Acetoxyphenyl)-2-butanone is used as an attractant in melon fly traps. This helps in monitoring and managing the population of these pests, which can cause significant damage to crops.
Used in Flavor and Fragrance Industry:
4-(4-Acetoxyphenyl)-2-butanone is also used in the flavor and fragrance industry due to its sweet, raspberry, and fruity odor. It is added to various food products to enhance their flavor and aroma.
Used in the Food Industry:
In the food industry, 4-(4-Acetoxyphenyl)-2-butanone is used as an additive in various categories, including:
Chewing gum: Usual use level is 5 ppm, with a maximum of 10 ppm.
Confectionary, frosting: Usual use level is 0.5 ppm, with a maximum of 1 ppm.
Fruit ices: Usual use level is 0.5 ppm, with a maximum of 1 ppm.
Gelatins, puddings: Usual use level is 1 ppm, with a maximum of 2 ppm.
Hard candy: Usual use level is 1 ppm, with a maximum of 2 ppm.
Imitation dairy: Usual use level is 0.2 ppm, with a maximum of 1 ppm.
Jams, jellies: Usual use level is 0.2 ppm, with a maximum of 1 ppm.
Nonalcoholic beverages: Usual use level is 0.2 ppm, with a maximum of 0.5 ppm.
Soft candy: Usual use level is 0.5 ppm, with a maximum of 2 ppm.
These usage levels ensure that the additive enhances the flavor and aroma of the food products without causing any adverse effects.
Identification
▼▲
CAS.No.:?
3572-06-3
FL.No.:?
09.288
FEMA.No.:?
3652
NAS.No.:?
3652
CoE.No.:?
n/a?
EINECS.No.:?
222-682-0?
JECFA.No.:?
731
Regulatory Status
CoE: n/a
FDA: n/a
FDA (other): n/a
JECFA: ADI: Acceptable. No safety concern at current levels of intake when used as a flavoring agent (2000).
Natural occurrence
Not reported found in nature.
Safety Profile
Moderately toxic by ingestion.When heated to decomposition it emits acrid smoke andirritating fumes.
Check Digit Verification of cas no
The CAS Registry Mumber 3572-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3572-06:
(6*3)+(5*5)+(4*7)+(3*2)+(2*0)+(1*6)=83
83 % 10 = 3
So 3572-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O3/c1-9(13)3-4-11-5-7-12(8-6-11)15-10(2)14/h5-8H,3-4H2,1-2H3
3572-06-3Relevant articles and documents
Photocatalytic Reductive Radical-Polar Crossover for a Base-Free Corey–Seebach Reaction
Crespi, Stefano,Donabauer, Karsten,K?nig, Burkhard,Murugesan, Kathiravan,Rozman, Ur?a
supporting information, p. 12945 - 12950 (2020/09/23)
A metal-free generation of carbanion nucleophiles is of prime importance in organic synthesis. Herein we report a photocatalytic approach to the Corey–Seebach reaction. The presented method operates under mild redox-neutral and base-free conditions giving the desired product with high functional group tolerance. The reaction is enabled by the combination of photo- and hydrogen atom transfer (HAT) catalysis. This catalytic merger allows a C?H to carbanion activation by the abstraction of a hydrogen atom followed by radical reduction. The generated nucleophilic intermediate is then capable of adding to carbonyl electrophiles. The obtained dithiane can be easily converted to the valuable α-hydroxy carbonyl in a subsequent step. The proposed reaction mechanism is supported by emission quenching, radical–radical homocoupling and deuterium labeling studies as well as by calculated redox-potentials and bond strengths.
Rational design, synthesis and structure-activity relationships of 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues as novel tyrosinase inhibitors
You, Ao,Zhou, Jie,Song, Senchuan,Zhu, Guoxun,Song, Huacan,Yi, Wei
, p. 924 - 931 (2015/03/04)
In continuing our program aimed to search for potent compounds as highly efficient tyrosinase inhibitors, here a series of novel 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues were designed, synthesized and their biological activities on mushroom tyrosinase were evaluated. Notably, most of compounds displayed remarkable tyrosinase inhibitory activities with IC50 value of lower than 1.0 μM. Furthermore, the structure-activity relationships (SARs) were discussed and the inhibition mechanism and the inhibitory kinetics of selected compounds 7k and 8d were also investigated. Taken together, these results suggested that such compounds could serve as the promising candidates for the treatment of tyrosinase-related disorders and further development of such compounds might be of great interest.