I3500
Indoxyl acetate
≥95% (GC)
Synonym(s):
3-Indolyl acetate, 3-Acetoxyindole
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About This Item
Empirical Formula (Hill Notation):
C10H9NO2
CAS Number:
Molecular Weight:
175.18
UNSPSC Code:
41106305
NACRES:
NA.51
PubChem Substance ID:
EC Number:
210-154-2
Beilstein/REAXYS Number:
143086
MDL number:
Product Name
Indoxyl acetate, ≥95% (GC)
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
SMILES string
CC(=O)Oc1c[nH]c2ccccc12
assay
≥95% (GC)
form
powder
mp
128-130 °C (lit.)
storage temp.
2-8°C
Quality Level
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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
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.
signalword
Warning
hcodes
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Quoc Trung Hua et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 35(4), 393-399 (2018-12-12)
Flow control-based paper devices have recently shown great potential for point-of-need analysis, since they allow for the easy operation of multi-step assays by minimizing user operation. In this work, a wax printing method was evaluated as a means to control
Soo-Kyoung Lee et al.
Foodborne pathogens and disease, 14(3), 141-147 (2017-02-06)
The present study analyzed the prevalence and molecular characterization of Campylobacter at different processing steps in poultry slaughterhouses to determine where contamination mainly occurs. A total of 1,040 samples were collected at four different stages (preprocessing cloacal swabs, postevisceration, postwashing
A Berry et al.
Journal of industrial microbiology & biotechnology, 28(3), 127-133 (2002-06-21)
A fermentation process was developed for production of indigo from glucose using recombinant Escherichia coli. This was achieved by modifying the tryptophan pathway to cause high-level indole production and adding the Pseudomonas putida genes encoding naphthalene dioxygenase (NDO). In comparison
Luis Collado et al.
International journal of systematic and evolutionary microbiology, 59(Pt 6), 1391-1396 (2009-06-09)
Three Arcobacter isolates, recovered from mussels (genus Mytilus), and one isolate from brackish water in Catalonia (north-east Spain) showed a novel pattern using a recently described identification method for members of the genus Arcobacter, 16S rRNA gene RFLP. Enterobacterial repetitive
C K Mills et al.
Journal of clinical microbiology, 25(8), 1560-1561 (1987-08-01)
One hundred and twelve Campylobacter strains comprising 15 species and subspecies were examined for their ability to hydrolyze indoxyl acetate. All strains of C. coli, C. cryaerophila, C. fennelliae, and C. jejuni hydrolyzed the compound, whereas three strains of C.
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