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Hexyl 3-bromopropanoate is a chemical compound with the molecular formula C9H17BrO2, classified as an alkyl bromo ester. It contains a bromine atom and an ester functional group, and is known for its sweet and fruity odor, reminiscent of pineapple.

6282-50-4

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6282-50-4 Usage

Uses

Used in Flavoring and Fragrance Industry:
Hexyl 3-bromopropanoate is used as a flavoring agent and fragrance ingredient for its sweet and fruity odor, resembling that of pineapple.
Used in Perfume Production:
Hexyl 3-bromopropanoate is used as a component in the production of perfumes, contributing to their sweet and fruity scent.
Used in Cosmetic Products:
Hexyl 3-bromopropanoate is used in the formulation of soaps and other cosmetic products, enhancing their fragrance and sensory appeal.
Used in Pharmaceutical Industry:
Hexyl 3-bromopropanoate has potential applications in the pharmaceutical industry, although specific uses are not detailed in the provided materials.
Used in Agricultural Industry:
Hexyl 3-bromopropanoate also has potential applications in the agricultural industry, but the specific uses are not specified in the provided materials.
Safety Precautions:
It is important to handle hexyl 3-bromopropanoate with caution, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 6282-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6282-50:
(6*6)+(5*2)+(4*8)+(3*2)+(2*5)+(1*0)=94
94 % 10 = 4
So 6282-50-4 is a valid CAS Registry Number.

6282-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name hexyl 3-bromopropanoate

1.2 Other means of identification

Product number -
Other names Hexyl 3-bromopropionate

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:6282-50-4 SDS

6282-50-4Downstream Products

6282-50-4Relevant academic research and scientific papers

Antimicrobial poly(2-methyloxazoline)s with bioswitchable activity through satellite group modification

Krumm, Christian,Harmuth, Simon,Hijazi, Montasser,Neugebauer, Britta,Kampmann, Anne-Larissa,Geltenpoth, Helma,Sickmann, Albert,Tiller, Joerg C.

, p. 3830 - 3834 (2014)

Biocides are widely used for preventing the spread of microbial infections and fouling of materials. Since their use can build up microbial resistance and cause unpredictable long-term environmental problems, new biocidal agents are required. In this study, we demonstrate a concept in which an antimicrobial polymer is deactivated by the cleavage of a single group. Following the satellite group approach, a biocidal quaternary ammonium group was linked through a poly(2-methyloxazoline) to an ester satellite group. The polymer with an octyl-3-propionoate satellite group shows very good antimicrobial activity against Gram-positive bacterial strains. The biocidal polymer was also found to have low hemotoxicity, resulting in a high HC50/MIC value of 120 for S. aureus. Cleaving the ester satellite group resulted in a 30-fold decrease in antimicrobial activity, proving the concept valid. The satellite group could also be cleaved by lipase showing that the antimicrobial activity of the new biocidal polymers is indeed bioswitchable. Biocides are widely used for preventing the spread of microbial infections and the fouling of materials. Since their application can build up microbial resistance and cause unpredictable long-term environmental problems, new biocidal agents are required. In a novel approach an antimicrobial polymer is deactivated by hydrolysis of an ester group through the action of a lipase. The crucial feature is the mutual interaction of the two endgroups of the polymer.

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