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2,2-Dimethyl-6-oxoheptanoic acid methyl ester, also known as ethyl 2,2-dimethyl-6-oxoheptanoate, is a colorless liquid chemical compound with the molecular formula C10H18O3. It is characterized by a fruity odor and is commonly utilized as a flavoring agent in the food and beverage industry. Additionally, it finds applications in the production of fragrances and serves as a solvent in various industrial processes. Due to its potential harmful effects when ingested, inhaled, or causing skin and eye irritation, careful handling and proper disposal are essential to mitigate environmental and health risks.

926-27-2

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926-27-2 Usage

Uses

Used in Food and Beverage Industry:
2,2-Dimethyl-6-oxoheptanoic acid methyl ester is used as a flavoring agent for imparting a fruity aroma and taste to various food and beverage products, enhancing their sensory appeal and consumer experience.
Used in Fragrance Production:
In the fragrance industry, 2,2-Dimethyl-6-oxoheptanoic acid methyl ester is employed as a key ingredient in creating a wide range of scent profiles, from fresh and fruity to more complex and nuanced aromas, contributing to the development of perfumes, colognes, and other scented products.
Used as an Industrial Solvent:
2,2-Dimethyl-6-oxoheptanoic acid methyl ester is utilized as a solvent in various industrial applications, including the manufacturing of coatings, adhesives, and cleaning agents, due to its ability to dissolve a wide range of substances and facilitate chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 926-27-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 926-27:
(5*9)+(4*2)+(3*6)+(2*2)+(1*7)=82
82 % 10 = 2
So 926-27-2 is a valid CAS Registry Number.

926-27-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,2-dimethyl-6-oxoheptanoate

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-heptan-6-on-1-carbonsaeure-methylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:926-27-2 SDS

926-27-2Downstream Products

926-27-2Relevant academic research and scientific papers

β-Carotene autoxidation: Oxygen copolymerization, non-vitamin A products, and immunological activity

Burton, Graham W.,Daroszewski, Janusz,Nickerson, James G.,Johnston, James B.,Mogg, Trevor J.,Nikiforov, Grigory B.

, p. 305 - 316 (2014/05/06)

Carotenoids are reported to have immunological effects independent of vitamin A activity. Although antioxidant activity has been suggested as a basis of action, the ability of carotenoids to autoxidize to numerous non-vitamin A products with immunological activity is an alternative yet to be fully explored. We have undertaken a systematic study of β-carotene autoxidation and tested the product mixture for immunological activity. Autoxidation proceeds predominantly by oxygen copolymerization, leading to a defined, reproducible product corresponding to net uptake of almost 8 molar equivalents of oxygen. The product, termed OxC-beta, empirical formula C40H60O 15 versus C40H56 for β-carotene, contains more than 30% oxygen (w/w) and 85% β-carotene oxygen copolymers (w/w) as well as minor amounts of many C8-C18 norisoprenoid compounds. No vitamin A or higher molecular weight norisoprenoids are present. The predominance of polymeric products has not been reported previously. The polymer appears to be a less polymerized form of sporopollenin, a biopolymer found in exines of spores and pollen. Autoxidations of lycopene and canthaxanthin show a similar predominance of polymeric products. OxC-beta exhibits immunological activity in a PCR gene expression array, indicating that carotenoid oxidation produces non-vitamin A products with immunomodulatory potential.

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