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Documenti fondamentali

PHR1049

Supelco

Gabapentin

Pharmaceutical Secondary Standard; Certified Reference Material

Sinonimo/i:

1-(Aminomethyl)-cyclohexaneacetic acid, Neurontin

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About This Item

Formula empirica (notazione di Hill):
C9H17NO2
Numero CAS:
Peso molecolare:
171.24
Beilstein:
2359739
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

certified reference material
pharmaceutical secondary standard

Livello qualitativo

agenzia

traceable to USP 1287303

Famiglia di API

gabapentin

CdA

current certificate can be downloaded

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

NCC1(CC(O)=O)CCCCC1

InChI

1S/C9H17NO2/c10-7-9(6-8(11)12)4-2-1-3-5-9/h1-7,10H2,(H,11,12)
UGJMXCAKCUNAIE-UHFFFAOYSA-N

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Descrizione generale

Gabapentin is an antiepileptic drug, which is a structural analog of γ-aminobu-tyric acid (GABA). It is used in the treatment of partial seizures in adults and children.
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Gabapentin is an anti-convulsant drug, which leads to the irreversible inhibition of the enzyme GABA-transaminase, thereby also prevents the physiological degradation of GABA in the brain.

Applicazioni

Gabapentin may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by chromatography, colorimetry and spectrophotometry.
Gabapentin may be used as a reference standard to validate the amount gabapentin present in the following:
  • In human plasma samples using high performance liquid chromatography (HPLC).
  • In pharmaceutical formulations using isocratic reversed-phase high performance liquid chromatography (RP-HPLC).
Gabapentin may be used pharmaceutical reference standard for the quantification of the analyte in pharmaceutical formulations using spectrophotometric technique.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Risultati analitici

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Altre note

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Nota a piè di pagina

To see an example of a Certificate of Analysis for this material enter LRAb7794 in the slot below. This is an example certificate only and may not be the lot that you receive.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

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Colorimetric determination of gabapentin in pharmaceutical formulation
Abdellatef HE and Khalil HM
Journal of Pharmaceutical and Biomedical Analysis, 31(1), 209-214 (2003)
Comparison of two aerosol-based detectors for the analysis of gabapentin in pharmaceutical formulations by hydrophilic interaction chromatography
Jia S, et al.
Talanta, 85(5), 2301-2306 (2011)
Veterinary Pharmacology and Therapeutics (2009)
Development and application of a validated HPLC method for the analysis of dissolution samples of gabapentin drug products
Gupta A, et al.
Journal of Pharmaceutical and Biomedical Analysis, 46, 181-186 (2008)
Spectrophotometric determination of gabapentin in pharmaceutical formulations using ninhydrin and p-acceptors
Siddiqui AF, et al.
European Journal of Medicinal Chemistry, 45(7), 2761-2767 (2010)

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