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Merck

I3500

Sigma-Aldrich

Indoxyl acetate

≥95% (GC)

Sinónimos:

3-Indolyl acetate, 3-Acetoxyindole

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About This Item

Fórmula empírica (notación de Hill):
C10H9NO2
Número de CAS:
Peso molecular:
175.18
Beilstein:
143086
Número CE:
Número MDL:
Código UNSPSC:
41106305
ID de la sustancia en PubChem:
NACRES:
NA.51

Análisis

≥95% (GC)

formulario

powder

mp

128-130 °C (lit.)

temp. de almacenamiento

2-8°C

cadena SMILES

CC(=O)Oc1c[nH]c2ccccc12

InChI

1S/C10H9NO2/c1-7(12)13-10-6-11-9-5-3-2-4-8(9)10/h2-6,11H,1H3

Clave InChI

JBOPQACSHPPKEP-UHFFFAOYSA-N

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Aplicación

Indoxyl acetate:
  • has been used to prepare free indoxyl for fermentor feeds and for in vitro 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) synthase inactivation assays
  • may be used as the potential substrate for the evaluation of carbonic anhydrases (CAs) esterase activity
  • may be used to prepare indoxyl acetate differential disk to evaluate the indoxyl acetate hydrolysis test for the differentiation of Campylobacter species

Acciones bioquímicas o fisiológicas

Indoxyl acetate (IA) can be used as a substrate to detect acetylcholinesterase (AChE) activity. It may also have the potential to be used as a suitable substrate for fast and easy detection of lipase activity.

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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J G Fox et al.
Journal of clinical microbiology, 38(7), 2546-2549 (2000-07-06)
We recently analyzed 11 helicobacter isolates cultured from diarrhea patients in Canada. These isolates had been characterized biochemically by restriction fragment length polymorphism (RFLP; AluI, HhaI) analysis and by fatty-acid analysis as Helicobacter pullorum. However, four of the isolates differed
Mantas Baliukynas et al.
Enzyme and microbial technology, 139, 109584-109584 (2020-08-01)
The interest in CO2 capture and conversion by biological methodologies into various beneficial products is increased. In nature, there are enzymes, with hydration activity, which catalyze the reversible hydration of the CO2 molecule and, thus, are of high interest for
J C Reitmeyer et al.
Journal of medical microbiology, 35(3), 148-151 (1991-09-01)
The biochemical characteristics of group G streptococci isolated from cats were markedly similar to the characteristics of group G streptococci from man. Both cat and human isolates of group G streptococci were also very similar in biochemical characteristics to group
Tomas Valek et al.
International journal of analytical chemistry, 2019, 8538340-8538340 (2019-12-31)
Lipases play a crucial role in metabolism of microbes, fungi, plants, and animals, and in analytical chemistry, they are often used in detection of fats and triglycerides. Determination of lipase activity is also important in toxicology, when lipase activity can
D S Hodge et al.
Journal of clinical microbiology, 28(6), 1482-1483 (1990-06-01)
Indoxyl acetate hydrolysis is a rapid, inexpensive differential test which can be performed easily to help identify campylobacter. A total of 571 Campylobacter cultures, including atypical variants, representing 10 species was tested.

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