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Informazioni su questo articolo
Formula empirica (notazione di Hill):
C8H19N
Numero CAS:
Peso molecolare:
129.24
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
Prezzi e disponibilità al momento non sono disponibili
Servizio Tecnico
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Permettici di aiutartigrade
pharmaceutical analytical impurity (PAI)
agency
USP
API family
octylamine
manufacturer/tradename
USP
application(s)
pharmaceutical small molecule
format
neat
storage temp.
-10 to -25°C
SMILES string
NC(CC(C)(C)C)(C)C
InChI
1S/C8H19N/c1-7(2,3)6-8(4,5)9/h6,9H2,1-5H3
InChI key
QIJIUJYANDSEKG-UHFFFAOYSA-N
General description
tert-Octylamine 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: Clavulanate Potassium
Therapeutic Area: Antibiotics
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: Clavulanate Potassium
Therapeutic Area: Antibiotics
Application
tert-Octylamine (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.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1C
Classe di stoccaggio
3 - Flammable liquids
flash_point_f
91.4 °F - closed cup
flash_point_c
33 °C - closed cup
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Numero articolo commerciale globale
| SKU | GTIN |
|---|---|
| 1A01310-25MG | 04065270921345 |



