Trimethylacetic anhydride

98%

Reagent Code: #240326
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Alias Trimethylacetic anhydride; 2,2-dimethylpropionic anhydride
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CAS Number 1538-75-6

science Other reagents with same CAS 1538-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.25 g/mol
Formula C₁₀H₁₈O₃
badge Registry Numbers
MDL Number MFCD00008842
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as a reagent in organic synthesis, this compound is effective for introducing the trimethylacetyl (pivaloyl) group into molecules. It is commonly employed in the preparation of pivaloyl-protected alcohols and amines, which serve as intermediates in pharmaceutical and agrochemical manufacturing. Its steric bulk helps reduce unwanted side reactions, making it valuable in selective acylations. It also finds use in the production of dyes, perfumes, and specialty esters due to its ability to form stable derivatives. In research laboratories, it acts as a dehydrating agent and derivatizing agent for analytical techniques.

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Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿290.00
inventory 25ml
10-20 days ฿460.00
inventory 500ml
10-20 days ฿3,350.00
inventory 2.5L
10-20 days ฿12,880.00
inventory 10L
10-20 days ฿51,200.00
inventory 100ml
10-20 days ฿1,320.00

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Trimethylacetic anhydride
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Used primarily as a reagent in organic synthesis, this compound is effective for introducing the trimethylacetyl (pivaloyl) group into molecules. It is commonly employed in the preparation of pivaloyl-protected alcohols and amines, which serve as intermediates in pharmaceutical and agrochemical manufacturing. Its steric bulk helps reduce unwanted side reactions, making it valuable in selective acylations. It also finds use in the production of dyes, perfumes, and specialty esters due to its ability to fo

Used primarily as a reagent in organic synthesis, this compound is effective for introducing the trimethylacetyl (pivaloyl) group into molecules. It is commonly employed in the preparation of pivaloyl-protected alcohols and amines, which serve as intermediates in pharmaceutical and agrochemical manufacturing. Its steric bulk helps reduce unwanted side reactions, making it valuable in selective acylations. It also finds use in the production of dyes, perfumes, and specialty esters due to its ability to form stable derivatives. In research laboratories, it acts as a dehydrating agent and derivatizing agent for analytical techniques.

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