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I3500

Indoxyl-Acetat

≥95% (GC)

Synonym(e):

3-Acetoxy-indol

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PackungsgrößeSKUVerfügbarkeitPreis
250 mg
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€ 60,90
1 g
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5 g
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Über diesen Artikel

Empirische Formel (Hill-System):
C10H9NO2
CAS-Nummer:
Molekulargewicht:
175.18
UNSPSC Code:
41106305
NACRES:
NA.51
PubChem Substance ID:
EC Number:
210-154-2
Beilstein/REAXYS Number:
143086
MDL number:

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Unterstützung erhalten

Quality Level

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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Dieser Artikel
259047H339863797
assay

≥95% (GC)

assay

99%

assay

≥99% (GC)

assay

≥80% (GC)

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

form

powder

form

solid

form

solid

form

-

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

storage temp.

2-8°C

mp

128-130 °C (lit.)

mp

100-102 °C (lit.)

mp

-

mp

-

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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Lagerklasse

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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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.
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.
G Douglas Inglis et al.
Applied and environmental microbiology, 72(6), 4464-4471 (2006-06-06)
Forty-two Helicobacter isolates were isolated from swine feces in The Netherlands and Denmark. All 12 isolates sequenced (16S rRNA gene) formed a robust clade with Helicobacter canadensis ( approximately 99% similarity). Species-specific PCR indicated that all of the isolates were
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
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

Global Trade Item Number

SKUGTIN
I3500-1G04061833856147
I3500-250MG04061833856154
I3500-5G04061833856161

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