Trimethyl orthoacetate

98%

Reagent Code: #239763
label
Alias Trimethyl orthoacetate; 1,1,1-trimethoxyethane, trimethyl acetate
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CAS Number 1445-45-0

science Other reagents with same CAS 1445-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 120.15 g/mol
Formula C₅H₁₂O₃
badge Registry Numbers
EC Number 215-892-9
MDL Number MFCD00008477
thermostat Physical Properties
Boiling Point 107-109 °C(lit.)
inventory_2 Storage & Handling
Density 0.944 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used as a water scavenger in esterification and acetalization reactions, helping to drive equilibrium toward product formation by removing water. Commonly employed in the synthesis of fragrances, flavors, and pharmaceuticals where moisture-sensitive intermediates are involved. Acts as a methylating agent in organic synthesis, particularly for introducing methoxy groups. Also utilized in the preparation of enol ethers and acetals, which serve as protecting groups or reactive intermediates in multi-step syntheses. Its ability to generate acetic acid upon hydrolysis makes it useful in controlled acid-release systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25ml
10-20 days ฿320.00
inventory 100ml
10-20 days ฿600.00
inventory 500ml
10-20 days ฿1,880.00
inventory 2.5L
10-20 days ฿7,320.00
inventory 25L
10-20 days ฿55,660.00
inventory 12X500ml
10-20 days ฿22,330.00
inventory 10L
10-20 days ฿25,600.00

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Trimethyl orthoacetate
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Used as a water scavenger in esterification and acetalization reactions, helping to drive equilibrium toward product formation by removing water. Commonly employed in the synthesis of fragrances, flavors, and pharmaceuticals where moisture-sensitive intermediates are involved. Acts as a methylating agent in organic synthesis, particularly for introducing methoxy groups. Also utilized in the preparation of enol ethers and acetals, which serve as protecting groups or reactive intermediates in multi-step sy

Used as a water scavenger in esterification and acetalization reactions, helping to drive equilibrium toward product formation by removing water. Commonly employed in the synthesis of fragrances, flavors, and pharmaceuticals where moisture-sensitive intermediates are involved. Acts as a methylating agent in organic synthesis, particularly for introducing methoxy groups. Also utilized in the preparation of enol ethers and acetals, which serve as protecting groups or reactive intermediates in multi-step syntheses. Its ability to generate acetic acid upon hydrolysis makes it useful in controlled acid-release systems.

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