4-(sec-Butoxy)-4-oxobutanoic acid

95%

Reagent Code: #46476
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CAS Number 100405-37-6

science Other reagents with same CAS 100405-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.1944 g/mol
Formula C₈H₁₄O₄
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MDL Number MFCD20648788
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in the synthesis of specialty chemicals and intermediates in organic chemistry. It serves as a building block in the production of polymers, coatings, and adhesives, where its ester functionality enhances flexibility and adhesion properties. Additionally, it finds application in the pharmaceutical industry for the development of drug delivery systems, leveraging its ability to modify solubility and bioavailability of active ingredients. In research, it is employed as a reagent for studying esterification and hydrolysis reactions.

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Test Parameter Specification
Appearance Light Yellow Liquid
Purity (%) 94.5-100
LC-MS Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,844.00

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4-(sec-Butoxy)-4-oxobutanoic acid
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Used primarily in the synthesis of specialty chemicals and intermediates in organic chemistry. It serves as a building block in the production of polymers, coatings, and adhesives, where its ester functionality enhances flexibility and adhesion properties. Additionally, it finds application in the pharmaceutical industry for the development of drug delivery systems, leveraging its ability to modify solubility and bioavailability of active ingredients. In research, it is employed as a reagent for studying

Used primarily in the synthesis of specialty chemicals and intermediates in organic chemistry. It serves as a building block in the production of polymers, coatings, and adhesives, where its ester functionality enhances flexibility and adhesion properties. Additionally, it finds application in the pharmaceutical industry for the development of drug delivery systems, leveraging its ability to modify solubility and bioavailability of active ingredients. In research, it is employed as a reagent for studying esterification and hydrolysis reactions.

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