85354-07-0 Usage
Description
Beta-apo-13-carotenone is an apo carotenoid compound that arises from the oxidative degradation of the beta,beta-carotene skeleton at the 13-position. It is a product of the breakdown of carotenoids, which are naturally occurring pigments found in plants, algae, and some bacteria. The oxidative degradation of the beta,beta-carotene skeleton leads to the formation of various apo carotenoid compounds, including beta-apo-13-carotenone.
Uses
Used in Antioxidant Applications:
Beta-apo-13-carotenone is used as an antioxidant in various industries, including food, cosmetics, and pharmaceuticals. Its antioxidant properties help protect cells from damage caused by reactive oxygen species (ROS) and free radicals, which can lead to various diseases and aging. By neutralizing these harmful molecules, beta-apo-13-carotenone can help maintain cellular health and prevent oxidative stress.
Used in Food Industry:
In the food industry, beta-apo-13-carotenone is used as a natural colorant and flavor enhancer. Its vibrant color can be used to add visual appeal to various food products, while its unique flavor profile can enhance the taste of different dishes. Additionally, its antioxidant properties can help extend the shelf life of food products by preventing oxidation and spoilage.
Used in Cosmetics Industry:
In the cosmetics industry, beta-apo-13-carotenone is used as an ingredient in various skincare and beauty products. Its antioxidant properties can help protect the skin from environmental damage, such as UV radiation and pollution, while also promoting skin health and reducing the signs of aging. Furthermore, its natural color can be used to add a subtle tint to cosmetics, providing a healthy glow to the skin.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, beta-apo-13-carotenone is used as a potential therapeutic agent for various health conditions. Its antioxidant properties can help treat or prevent diseases associated with oxidative stress, such as cardiovascular diseases, neurodegenerative disorders, and certain types of cancer. Additionally, its potential anti-inflammatory and immunomodulatory effects may also contribute to its therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 85354-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85354-07:
(7*8)+(6*5)+(5*3)+(4*5)+(3*4)+(2*0)+(1*7)=140
140 % 10 = 0
So 85354-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O/c1-14(8-6-10-16(3)19)11-12-17-15(2)9-7-13-18(17,4)5/h6,8,10-12H,7,9,13H2,1-5H3/b10-6-,12-11-,14-8-
85354-07-0Relevant articles and documents
Efficient generation of a trisporoid library by combination of synthesis and biotransformation
Schachtschabel, Doreen,Boland, Wilhelm
, p. 1366 - 1372 (2007/10/03)
(Chemical Equation Presented) Trisporic acids and their biosynthetic precursors represent a family of powerful fungal pheromones and morphogenetic factors. A highly flexible synthetic protocol is described that (i) provides rapid access to nonfunctionaliz
Polyvinylogation Reagents: 1-Lithio-4-trimethylsiloxy-penta-1,3-diene and 1-Lithio-4-ethoxy-2-methyl-buta-1,3-diene
Duhamel, Lucette,Ancel, Jean-Erick
, p. 9237 - 9250 (2007/10/02)
Title products, lithiodienol ethers 6a and 7a, synthetic equivalents of 4-lithio pent-3-ene-2-one and 4-lithio-senecialdehyde were obtained by bromine-lithium exchange.They are choice reagents for the transformations 1 -> 2 and 1 -> 3, respectively.
A CONVENIENT ROUTE TO α,β-UNSATURATED METHYL KETONES APPLICATION TO RETINAL ANALOGUE SYNTHESIS
Croteau, Allan A.,Termini, John
, p. 2481 - 2484 (2007/10/02)
Deprotonated ketimines 1a,b add to aldehydes and ketones to provide tri- and tetra-substituted α,β-unsaturated methyl ketones 2a,b with substantial percentage of Z-geometry which are not readily accessible by other methods.
