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Acrylic acid isoamyl ester is a chemical compound characterized by its fruity, apple-like odor. It is a clear, colorless liquid with a high boiling point and low volatility, produced through the esterification of acrylic acid with isoamyl alcohol. This ester is primarily used as a flavoring agent and fragrance ingredient in various applications due to its pleasant scent.

4245-35-6

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4245-35-6 Usage

Uses

Used in Perfumery and Personal Care Products:
Acrylic acid isoamyl ester is used as a fragrance ingredient for its fruity, apple-like odor, adding a pleasant scent to perfumes and personal care products.
Used in Food and Beverage Flavorings:
This ester is used as a flavoring agent in the food and beverage industry to impart a fruity taste, enhancing the overall flavor profile of various products.
Used in Industrial Applications:
Acrylic acid isoamyl ester is used as a solvent in various industrial applications, such as inks, adhesives, and coatings, due to its solvent properties and compatibility with different materials.
Used in the Production Process:
Acrylic acid isoamyl ester is produced through the esterification of acrylic acid with isoamyl alcohol, resulting in a compound with a high boiling point and low volatility, suitable for various applications.
It is important to handle acrylic acid isoamyl ester with care due to its potential irritant and flammable properties, ensuring safety in its use across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 4245-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4245-35:
(6*4)+(5*2)+(4*4)+(3*5)+(2*3)+(1*5)=76
76 % 10 = 6
So 4245-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-4-8(9)10-6-5-7(2)3/h4,7H,1,5-6H2,2-3H3

4245-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbutyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names Acrylic Acid Isopentyl Ester

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:4245-35-6 SDS

4245-35-6Relevant academic research and scientific papers

Rational Design of Single-Chain Polymeric Nanoparticles That Kill Planktonic and Biofilm Bacteria

Nguyen, Thuy-Khanh,Lam, Shu Jie,Ho, Kitty K. K.,Kumar, Naresh,Qiao, Greg G.,Egan, Suhelen,Boyer, Cyrille,Wong, Edgar H. H.

, p. 237 - 248 (2017/04/21)

Infections caused by multidrug-resistant bacteria are on the rise and, therefore, new antimicrobial agents are required to prevent the onset of a postantibiotic era. In this study, we develop new antimicrobial compounds in the form of single-chain polymeric nanoparticles (SCPNs) that exhibit excellent antimicrobial activity against Gram-negative bacteria (e.g., Pseudomonas aeruginosa) at micromolar concentrations (e.g., 1.4 μM) and remarkably kill ≥99.99% of both planktonic cells and biofilm within an hour. Linear random copolymers, which comprise oligoethylene glycol (OEG), hydrophobic, and amine groups, undergo self-folding in aqueous systems due to intramolecular hydrophobic interactions to yield these SCPNs. By systematically varying the hydrophobicity of the polymer, we can tune the extent of cell membrane wall disruption, which in turn governs the antimicrobial activity and rate of resistance acquisition in bacteria. We also show that the incorporation of OEG groups into the polymer design is essential in preventing complexation with proteins in biological medium, thereby maintaining the antimicrobial efficacy of the compound even in in vivo mimicking conditions. In comparison to the last-resort antibiotic colistin, our lead agents have a higher therapeutic index (by ca. 2-3 times) and hence better biocompatibility. We believe that the SCPNs developed here have potential for clinical applications and the information pertaining to their structure-activity relationship will be valuable toward the general design of synthetic antimicrobial (macro)molecules.

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