About This Item
Fórmula empírica (Notação de Hill):
C12H10OS
Número CAS:
Peso molecular:
202.27
Número MDL:
Código UNSPSC:
12352204
ID de substância PubChem:
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
CC(=O)Sc1ccc2ccccc2c1
InChI
1S/C12H10OS/c1-9(13)14-12-7-6-10-4-2-3-5-11(10)8-12/h2-8H,1H3
chave InChI
NMFMUXYHGNUOAI-UHFFFAOYSA-N
Código de classe de armazenamento
13 - Non 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
Eyeshields, Gloves, type N95 (US)
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Iu G Zhukovskiĭ et al.
Ukrains'kyi biokhimichnyi zhurnal (1999 ), 75(3), 67-70 (2003-10-28)
1- and 2-thionaphthylacetates were tested as cholinesterase substrates. It was shown that the butyrilcholinesterase from horse serum can hydrolize these compounds. The hydrolysis velocity of 1-thionaphthylacetate was comparable with hydrolysis velocity of acetylthiocholine (the well known cholinesterase substrate), but 2-thionaphthylacetate
B C Payne et al.
The Histochemical journal, 12(1), 71-86 (1980-01-01)
Using the substrate 2-naphthylthiol acetate (NTA), we developed a reproducible method of demonstrating a non-specific esterase while retaining nuclear and cytoplasmic details at the ultrastructural level. The NTA esterase had a distribution and pattern of staining similar to those of
H L Li et al.
Experimental and molecular pathology, 46(3), 321-330 (1987-06-01)
Nonspecific esterase activity was localized ultrastructurally within normal and leukemic hematopoietic cells by the use of 2-naphthylthiol acetate (NTA) as a substrate. NTA esterase activity was identified in all cell lines, although mononuclear phagocytes contained the most abundant activity. Monocytes
P L Sannes et al.
The Histochemical journal, 17(1), 43-56 (1985-01-01)
A 2-thionaphthyl acetate substrate was utilized to assess the subcellular distribution of nonspecific esterases in rat pulmonary alveolar and peritoneal macrophages. The enzymatically liberated 2-thionaphthol was visualized at pH 7.1 by utilizing gold as a capture agent. Glutaraldehyde-fixed macrophages derived
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