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I3500

Sigma-Aldrich

Indoxyl acetate

≥95% (GC)

Synonym(s):

3-Indolyl acetate, 3-Acetoxyindole

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250 MG
$60.60
1 G
$78.62
5 G
$273.70

About This Item

Empirical Formula (Hill Notation):
C10H9NO2
CAS Number:
608-08-2
Molecular Weight:
175.18
Beilstein/REAXYS Number:
143086
EC Number:
210-154-2
MDL number:
MFCD00014561
UNSPSC Code:
41106305
PubChem Substance ID:
24896038
NACRES:
NA.51

$60.60

List price$71.30Save 15%
Web-Only Promotion

Available to ship onApril 08, 2025Details

assay

≥95% (GC)

form

powder

mp

128-130 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI key

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[1]
  • may be used as the potential substrate for the evaluation of carbonic anhydrases (CAs) esterase activity[2]
  • may be used to prepare indoxyl acetate differential disk to evaluate the indoxyl acetate hydrolysis test for the differentiation of Campylobacter species[3]

Biochem/physiol Actions

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.[4]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN0782
BCCL4919
BCCM3849
BCCK2376
BCCK5609

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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
F Villatte et al.
BioTechniques, 30(1), 81-84 (2001-02-24)
The synaptic enzyme acetylcholinesterase (AChE), which is the target of many insecticides and potential warfare agents, is implied in Alzheimer's disease and is a good potential candidate to be used in biosensors. This promotes a strong demand for production of
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