T14001
3,4,5,6-Tetrahydrophthalic anhydride
95%
Sinônimo(s):
Cyclohexene-1,2-dicarboxylic anhydride
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10 G
R$ 1.883,00
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10 G
R$ 1.883,00
About This Item
Fórmula empírica (Notação de Hill):
C8H8O3
Número CAS:
Peso molecular:
152.15
Beilstein:
136335
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de substância PubChem:
NACRES:
NA.23
Produtos recomendados
Nível de qualidade
Ensaio
95%
pf
69-73 °C (lit.)
cadeia de caracteres SMILES
O=C1OC(=O)C2=C1CCCC2
InChI
1S/C8H8O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H2
chave InChI
HMMBJOWWRLZEMI-UHFFFAOYSA-N
Procurando produtos similares? Visita Guia de comparação de produtos
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Aquatic Chronic 3 - Eye Dam. 1 - Resp. Sens. 1 - Skin Sens. 1
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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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
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
[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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