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Über diesen Artikel
Empirische Formel (Hill-System):
C6H10O6
CAS-Nummer:
Molekulargewicht:
178.14
MDL number:
NACRES:
NA.24
Preise und Verfügbarkeit sind derzeit nicht verfügbar.
Technischer Dienst
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Unterstützung erhaltengrade
pharmaceutical analytical impurity (PAI)
agency
USP
API family
canagliflozin
manufacturer/tradename
USP
mp
142-144 °C (lit.)
application(s)
pharmaceutical small molecule
format
neat
storage temp.
-10 to -25°C
SMILES string
OC[C@@H]1OC(=O)[C@@H](O)[C@H](O)[C@H]1O
InChI key
PHOQVHQSTUBQQK-KLVWXMOXSA-N
General description
L-Glucono-δ-lactone 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: Canagliflozin
Therapeutic Area: Endocrine
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: Canagliflozin
Therapeutic Area: Endocrine
Application
L-Glucono-δ-lactone (USP PAI) 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
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| 1A04500-25MG | 04065270913647 |