Merck
CN

T14001

Sigma-Aldrich

3,4,5,6-四氢邻苯二甲酸酐

95%

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别名:
1,2-环己烯二羧酸酐
Empirical Formula (Hill Notation):
C8H8O3
CAS号:
分子量:
152.15
Beilstein:
136335
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.23

质量水平

检测方案

95%

mp

69-73 °C (lit.)

SMILES string

O=C1OC(=O)C2=C1CCCC2

InChI

1S/C8H8O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H2

InChI key

HMMBJOWWRLZEMI-UHFFFAOYSA-N

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此商品
217808797995136891
cis-Aconitic anhydride 95%

Sigma-Aldrich

217808

顺式乌头酸酐

Phthalic anhydride anhydrous, free-flowing, Redi-Dri™, ACS reagent, ≥99%

Sigma-Aldrich

797995

邻苯二甲酸酐

mp

69-73 °C (lit.)

mp

75-78 °C (lit.)

mp

131-134 °C (lit.)

mp

97-103 °C (lit.)

象形图

CorrosionHealth hazard

警示用语:

Danger

危险分类

Aquatic Chronic 3 - Eye Dam. 1 - Resp. Sens. 1 - Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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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A Ikai et al.
The Journal of biological chemistry, 265(14), 8280-8284 (1990-05-15)
As a model for the molecular structure of proteins belonging to the alpha 2-macroglobulin family, ovomacroglobulin of reptilian origin was studied by electron microscopy in the original tetrameric form as well as in the dissociated forms into half- and quarter
L I O'Connell et al.
Archives of biochemistry and biophysics, 263(2), 315-322 (1988-06-01)
Modification of glutamate dehydrogenase with 3,4,5,6-tetrahydrophthalic anhydride at pH 8.0 results in the progressive loss of enzymatic activity and a concomitant increase in the negative charge of the protein. Although the rate of inactivation at room temperature is too rapid
J B Swaney
Journal of lipid research, 24(3), 245-252 (1983-03-01)
Trypsin digestion of human high density lipoprotein (d 1.125-1.21 g/ml) on which the lysine residues have been masked with the reversible blocking group, 2,3,4,5-tetrahydrophthallic anhydride (THPA), was found to result in the fragmentation of the apoA-I component, but not the
Subat Turdi et al.
Toxicology letters, 178(3), 197-201 (2008-05-10)
Doxorubicin is an effective anthracycline used for cancer therapy. However, the clinical application of doxorubicin has been largely limited by its irreversible cardiotoxicity, which is mainly induced by the primary amine group. In this study, we structurally modified doxorubicin by
[Data providing a basis for the MPEL of tetrahydrophthalic anhydride, tetrahydrophthalamide and hydroxymethyltetrahydrophthalimide in the air of the work environment].
A I Gurova et al.
Gigiena truda i professional'nye zabolevaniia, (12)(12), 37-38 (1985-12-01)

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