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I3500

Sigma-Aldrich

Indoxyl acetate

≥95% (GC)

Synonyme(s) :

3-Indolyl acetate, 3-Acetoxyindole

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About This Item

Formule empirique (notation de Hill):
C10H9NO2
Numéro CAS:
608-08-2
Poids moléculaire :
175.18
Numéro Beilstein :
143086
Numéro CE :
210-154-2
Numéro MDL:
MFCD00014561
Code UNSPSC :
41106305
ID de substance PubChem :
24896038
Nomenclature NACRES :
NA.51

Niveau de qualité

200

Pureté

≥95% (GC)

Forme

powder

Pf

128-130 °C (lit.)

Température de stockage

2-8°C

Chaîne 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

Clé InChI

JBOPQACSHPPKEP-UHFFFAOYSA-N

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Application

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

Actions biochimiques/physiologiques

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.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H315,H319,H335

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

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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
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
Simon J G Otto et al.
Foodborne pathogens and disease, 17(3), 178-186 (2019-10-30)
To describe a historical baseline of antimicrobial resistance (AMR) profiles for human clinical Campylobacter species isolates obtained by laboratory surveillance in the province of Saskatchewan from 1999 to 2006; to determine if there were differences in resistance between Campylobacter jejuni
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
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