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Merck
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文件

8.22278

Sigma-Aldrich

Acetic anhydride

for synthesis

别名:

Acetic anhydride, Acetyl acetate, Acetyl oxide

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About This Item

线性分子式:
(CH3CO)2O
CAS号:
分子量:
102.09
MDL號碼:
分類程式碼代碼:
12352106
酶委員會索引編號:
203-564-8
NACRES:
NA.22

蒸汽壓力

4 hPa ( 20 °C)

品質等級

化驗

≥98.0% (GC)

形狀

liquid

自燃溫度

330 °C

效力

630 mg/kg LD50, oral (Rat)
4320 mg/kg LD50, skin (Rabbit)

expl. lim.

2.0-10.2 % (v/v)

pH值

3 (20 °C, 10 g/L in H2O)

mp

-73 °C

轉變溫度

flash point 49 °C

密度

1.08 g/cm3 at 20 °C

儲存溫度

2-30°C

InChI

1S/C4H6O3/c1-3(5)7-4(2)6/h1-2H3

InChI 密鑰

WFDIJRYMOXRFFG-UHFFFAOYSA-N

一般說明

Acetic anhydride is a widely used reagent in organic synthesis. The reagent is effective for acetylating alcohols, amines, and thiols. Additionally, it is used in various named reactions such as the Pummerer reaction, the Perkin reaction, the Polonovski reaction, the N-oxide reaction, and the Thiele reaction. Acetic anhydride is an effective reagent during oxidation of alcohols, dehydration, ether cleavage, enol acetate formation, and gem-diacetate formation.

應用

Acetic anhydride is used:
  • In the solvent free acylation of 2-methylfuran to 2-acetyl-5-methylfuran in presence of hydroxide fluorides catalyst.
  • As a catalyst in the synthesis of 3-arylideneisobenzofuran-1(3H)-one derivatives from phthalic anhydride and quinoline derivatives.
  • In the preparation of hyperbranched poly ethoxy siloxanes by condensation reaction with tetra ethoxy silane in presence of an organotitanium catalyst.

分析報告

Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.080 - 1.082
Identity (IR): passes test

訊號詞

Danger

危險分類

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

120.2 °F - closed cup

閃點(°C)

49 °C - closed cup


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访问文档库

Inorganic hydroxide fluorides as solid catalysts for acylation of 2-methylfuran by acetic anhydride
Frouri F, et al.
Applied Catalysis. B, Environmental, 168, 515-523 (2015)
Acetic Anhydride
Regina Zibuck
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
One-pot synthesis of hyperbranched polyethoxysiloxanes
Zhu X, et al.
Macromolecules, 39(5), 1701-1708 (2016)

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