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Merck
CN

125733

Sigma-Aldrich

邻苯二甲酸酐

99%, flakes, ReagentPlus®

别名:

1,2-Benzenedicarboxylic anhydride, 1,3-Isobenzofurandione, Phthalic acid anhydride

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关于此项目

经验公式(希尔记法):
C8H4O3
化学文摘社编号:
分子量:
148.12
Beilstein:
118515
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.21
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产品名称

邻苯二甲酸酐, ReagentPlus®, 99%

蒸汽密度

5.1 (vs air)

质量水平

蒸汽压

<0.01 mmHg ( 20 °C)

产品线

ReagentPlus®

方案

99%

表单

flakes

自燃温度

1058 °F

expl. lim.

10.4 %

沸点

284 °C (lit.)

mp

131-134 °C (lit.)

官能团

anhydride
ester

SMILES字符串

O=C1OC(=O)c2ccccc12

InChI

1S/C8H4O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H

InChI key

LGRFSURHDFAFJT-UHFFFAOYSA-N

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一般描述

Phthalic anhydride is an industrially important chemical. It can be prepared from o-xylene or naphthalene. It is widely used for the industrial preparation of plasticizers for PVC (polyvinyl chloride).
Phthalic anhydride can be synthesized via oxidation of o-xylene, in the presence of V2O5/TiO2 monolithic catalyst supported by aluminium honeycomb.

应用

Phthalic anhydride may be used in the synthesis of the following compounds:
  • pthalimide
  • phenolphthalein
  • anthracene

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

305.6 °F - DIN 51758

闪点(°C)

152 °C - DIN 51758

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

"Conductive monolithic catalysts: development and industrial pilot tests for the oxidation of o-xylene to phthalic anhydride"
Groppi G, et al.
Industrial & Engineering Chemistry Research, 51(22), 7590-7596 (2011)
Phthalic anhydride from o-xylene catalysis: science and engineering.
Nikolov V, et al.
Catalysis Reviews: Science and Engineering, 33(3-4), 319-374 (1991)
Eagleson M.
Concise Encyclopedia Chemistry, 77-77 (1994)
Catalysts, kinetics and reactor design in phthalic anhydride synthesis.
Wainwright MS and Foster NR.
Catalysis Reviews: Science and Engineering, 19(2), 211-292 (1979)
Chuan-Fu Liu et al.
Journal of agricultural and food chemistry, 55(6), 2399-2406 (2007-02-27)
Homogeneous modification of cellulose, isolated with 10% KOH from delignified sugarcane bagasse, was performed in room-temperature ionic liquid 1-allyl-3-methylinidazolium chloride with phthalic anhydride in the absence of catalyst. The results showed the degree of substitution of phthalated cellulosic derivatives, ranging

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