Trimethylacetic anhydride
Trimethylacetic anhydride ??
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193 °C(lit.)
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0.918 g/mL at 25 °C(lit.)
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62.1Pa at 25℃
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n 20/D 1.409(lit.)
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135 °F
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Inert atmosphere,Room Temperature
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Moisture Sensitive
BRN
386552
InChI
InChI=1S/C10H18O3/c1-9(2,3)7(11)13-8(12)10(4,5)6/h1-6H3
InChIKey
PGZVFRAEAAXREB-UHFFFAOYSA-N
SMILES
C(C)(C)(C)C(=O)OC(=O)C(C)(C)C
LogP
2.15
CAS ??????
1538-75-6(CAS DataBase Reference)
EPA
Propanoic acid, 2,2-dimethyl-, anhydride (1538-75-6)
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C
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34
?????
26-36/37/39-45
????(UN No.)
UN 2920 8/PG 2
WGK ??
3
F ??????
9-13-21
TSCA
Yes
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8
????
II
HS ??
29159000
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Danger
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P- ??
H226
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H314
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?? 1A, B, C
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P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
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P210
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P233
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P240
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P280
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P303+P361+P353
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P305+P351+P338
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NFPA 704
Trimethylacetic anhydride C??? ??, ??, ??
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Trimethylacetic anhydride is a pivalic acid derivative that is used in organic synthesis. The compound's reaction mechanism is believed to be the formation of an alkanoic acid, which reacts with a hydroxyl group to form an anhydride. Trimethyl acetic anhydride has been shown to have pharmacokinetic properties and can be used as a nonsteroidal anti-inflammatory drug. This compound has also been found to have a matrix effect on crystalline cellulose and is capable of forming nitrogen-containing carboxylic acids.
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clear colourless liquid
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Trimethylacetic anhydride was used:
in solid-phase oligonucleotide synthesis in kinetic resolution of racemic 2-hydroxy-γ-butyrolactones with diphenylacetic acid as acylation and esterification reagent for anilines as acylation and esterification reagent for phenols
Trimethylacetic anhydride ?? ?? ? ???
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Trimethylacetic anhydride ?? ??
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Americas 1
Belgium 1
Canada 1
China 198
Europe 1
France 1
Germany 4
India 8
Japan 3
Slovakia 1
South Korea 2
Switzerland 5
United Kingdom 5
United States 24
Global 255
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Trimethylacetic anhydride ?? ??: