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Documentos Principais

186341

Sigma-Aldrich

1-Naphthalenesulfonic acid

>50%

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About This Item

Fórmula linear:
C10H7SO3H
Número CAS:
Peso molecular:
208.23
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Formulário

solid

Nível de qualidade

concentração

>50%

pf

77-79 °C (lit.)

solubilidade

alcohol: freely soluble
diethyl ether: slightly soluble
water: freely soluble

cadeia de caracteres SMILES

OS(=O)(=O)c1cccc2ccccc12

InChI

1S/C10H8O3S/c11-14(12,13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H,11,12,13)

chave InChI

PSZYNBSKGUBXEH-UHFFFAOYSA-N

Informações sobre genes

Descrição geral

Mechanism of metabolism of 1-naphthalenesulfonic acid by green algae Scenedesmus obliquus has been investigated.

Aplicação

1-Naphthalenesulfonic acid was used as template molecule to prepare new non-covalent molecularly imprinted polymer for solid-phase extraction of naphthalene sulfonates.

Outras notas

remainder naphthalenesulfonic acid, sulfuric acid and water

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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International journal of biological macromolecules, 101, 32-39 (2017-03-23)
The α-glucosidase inhibitor is of interest to researchers due to its association with type-2 diabetes treatment. Hesperetin is a flavonoid with natural antioxidant properties. This paper presents an evaluation on the effects of hesperetin on α-glucosidase via inhibitory kinetics using
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We have systemically investigated unusual elution behaviors of an IgG4 (mAb A) in cation exchange chromatography (CEX). This mAb A exhibited two elution peaks under certain conditions when being purified by several strong CEX columns. When either of the two
Ester Caro et al.
Journal of chromatography. A, 1047(2), 175-180 (2004-10-06)
A new polymeric sorbent synthesised by exploiting molecular imprinting technology has been used to selectively extract naphthalene sulfonates (NSs) directly from aqueous samples. In the non-covalent molecular imprinting approach used to prepare this polymer, 1-naphthalene sulfonic acid (1-NS) and 4-vinylpyridine

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