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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C9H9N3O2
Numer CAS:
Masa cząsteczkowa:
191.19
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
Pomoc techniczna
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Pozwól nam pomócgrade
pharmaceutical analytical impurity (PAI)
agency
USP
manufacturer/tradename
USP
application(s)
pharmaceutical small molecule
format
neat
storage temp.
2-8°C
SMILES string
[N+](=O)([O-])c1cc2[n](nc(c2cc1)C)C
InChI
1S/C9H9N3O2/c1-6-8-4-3-7(12(13)14)5-9(8)11(2)10-6/h3-5H,1-2H3
InChI key
RUTULKJFQZYUDG-UHFFFAOYSA-N
General description
Find answers to frequently asked questions on USP products in USP FAQs.
1,3-Dimethyl-6-nitroindazole is a USP Pharmaceutical Analytical Impurity (PAI).
USP PAI are a product line of impurities suitable for research and analytical purposes, which help to ensure the quality and safety of medicines.
Associated Drug Substance: Pazopanib
Therapeutic Area: Oncology
For more information about this PAI, visit here.
USP PAI are a product line of impurities suitable for research and analytical purposes, which help to ensure the quality and safety of medicines.
Associated Drug Substance: Pazopanib
Therapeutic Area: Oncology
For more information about this PAI, visit here.
Application
1,3-Dimethyl-6-nitroindazole is intended for use in analytical testing to detect, identify, and measure pharmaceutical impurities.
Features and Benefits
USP PAI advance your early analytical R&D and process development. PAI can be used in the following applications:
1. Conduct analytical tests during early formulation feasibility studies.
2. Determine degradation impurities produced during stress studies.
3. Develop, validate, and transfer analytical methods.
4. Perform spiking studies during process R&D to demonstrate depletion upon recrystallization.
5. Record retention times and/or spectra
6. Determine relative response factors.
7. Identify unknown impurities that formed during ICH stability conditions.
8. Identify impurities that are present in the Reference Listed Drug
9. Test for and profile impurities not listed in drug substance and drug product monographs.
1. Conduct analytical tests during early formulation feasibility studies.
2. Determine degradation impurities produced during stress studies.
3. Develop, validate, and transfer analytical methods.
4. Perform spiking studies during process R&D to demonstrate depletion upon recrystallization.
5. Record retention times and/or spectra
6. Determine relative response factors.
7. Identify unknown impurities that formed during ICH stability conditions.
8. Identify impurities that are present in the Reference Listed Drug
9. Test for and profile impurities not listed in drug substance and drug product monographs.
Analysis Note
Produkty te są przeznaczone wyłącznie do testów i oznaczeń. Nie są one przeznaczone do podawania ludziom lub zwierzętom i nie mogą być stosowane do diagnozowania, leczenia lub wyleczenia jakichkolwiek chorób.
Other Notes
Sales restrictions may apply.
Ta strona może zawierać tekst przetłumaczony maszynowo.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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