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250 MG
292,00 zł
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C10H9NO2
Numer CAS:
Masa cząsteczkowa:
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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Pomoc techniczna
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Pozwól nam pomócassay
≥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
1 of 4
Ta pozycja | |||
|---|---|---|---|
| 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]
Ta strona może zawierać tekst przetłumaczony maszynowo.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Klasa składowania
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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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
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
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
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
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| I3500-1G | 04061833856147 |
| I3500-250MG | 04061833856154 |
| I3500-5G | 04061833856161 |
Active Filters
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