Methyl trimethylacetate

99%

Reagent Code: #205862
label
Alias Methyl trimethyl acetate; methyl 2,2-dimethylpropionate; methyl tert-valerate
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CAS Number 598-98-1

science Other reagents with same CAS 598-98-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 116.16 g/mol
Formula C₆H₁₂O₂
badge Registry Numbers
MDL Number MFCD00008843
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as a solvent and intermediate in organic synthesis, this compound is valued for its stability and reactivity in esterification processes. It serves in the production of pharmaceuticals, agrochemicals, and specialty esters due to its ability to participate in condensation reactions. Its steric hindrance from the bulky tert-butyl-like group makes it useful in controlled reactions where selective reactivity is required. Additionally, it finds use in fragrance formulations for its mild ester odor and solvency properties.

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Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿300.00
inventory 25ml
10-20 days ฿430.00
inventory 500ml
10-20 days ฿3,550.00
inventory 2.5L
10-20 days ฿15,350.00
inventory 100ml
10-20 days ฿1,000.00

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Methyl trimethylacetate
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Used primarily as a solvent and intermediate in organic synthesis, this compound is valued for its stability and reactivity in esterification processes. It serves in the production of pharmaceuticals, agrochemicals, and specialty esters due to its ability to participate in condensation reactions. Its steric hindrance from the bulky tert-butyl-like group makes it useful in controlled reactions where selective reactivity is required. Additionally, it finds use in fragrance formulations for its mild ester o

Used primarily as a solvent and intermediate in organic synthesis, this compound is valued for its stability and reactivity in esterification processes. It serves in the production of pharmaceuticals, agrochemicals, and specialty esters due to its ability to participate in condensation reactions. Its steric hindrance from the bulky tert-butyl-like group makes it useful in controlled reactions where selective reactivity is required. Additionally, it finds use in fragrance formulations for its mild ester odor and solvency properties.

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