Gabapentin Reference Standard (CAS 60142-96-3) and Impurity Standards: Key Factors in Pharmaceutical Testing

Gabapentin, a crucial active pharmaceutical ingredient (API) in the treatment of epilepsy, neuropathic pain, hot flashes, and other anxiety disorders, is increasingly asserting its indispensable role in the medical field. This API can inhibit the neurotransmitter γ-aminobutyric acid (GABA). To ensure the therapeutic efficacy and absolute safety of the drug, strict quality control through Gabapentin reference standards (CAS 60142-96-3) and Gabapentin impurity standards is extremely essential. This article will delve into the importance of Gabapentin and introduce reliable solutions for providing reference and impurity standards, meeting the most stringent requirements of the pharmaceutical industry.

Detailed information about Gabapentin Reference Standard:

• Chemical name: Gabapentin
• CAS number: 60142-96-3
• Molecular formula: C9H17NO2
• Molecular weight: 171.24
• Synonyms: 1-(Aminomethyl)cyclohexaneacetic Acid; Neurontin; GOE-3450; Cyclohexaneacetic acid, 1-(aminomethyl) (USP)
• Classification: Pharmaceutical standard, intermediate, pure chemical
• Appearance: White to off-white solid
• Storage conditions: 2-8°C (refrigerator)
• Shipping conditions: Ambient temperature
• Application: As an anticonvulsant and antiepileptic drug, Gabapentin is used to treat epilepsy, neuropathic pain, hot flashes, and other anxiety disorders. It can inhibit the neurotransmitter γ-aminobutyric acid (GABA).

Overriding Importance of Gabapentin Reference Standards and Impurity Standards

In the field of pharmaceutical manufacturing and testing, quality control is a crucial factor in ensuring the safety, efficacy, and regulatory compliance of products. For Gabapentin, the use of pharmaceutical reference standards and Gabapentin impurity standards plays an extremely important role in many aspects:

• Qualitative and Quantitative Analysis: Gabapentin reference standard (CAS 60142-96-3) helps accurately determine the Gabapentin content in the final product, ensuring correct dosage and therapeutic efficacy.
• Purity Control: Gabapentin impurity standards help evaluate the presence and content of impurities that may arise during synthesis or storage. Impurity control is mandatory to prevent unwanted substances from affecting drug quality and safety.
• Research and Development (R&D): Reference standards and impurity standards support the API synthesis process, formula optimization, and stability testing of Gabapentin under various conditions.
• Ensuring Compliance with International Pharmacopoeia: The use of pharmacopoeial reference standards and impurity standards (such as EP, BP) is a mandatory requirement for pharmaceutical manufacturers to comply with strict industry regulations, thereby ensuring products are allowed to circulate in the global market.

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Reliable Source for Gabapentin Reference Standards and Impurity Standards

We pride ourselves on being a reputable supplier of high-quality Gabapentin reference standards (CAS 60142-96-3) and Gabapentin impurity standards, fully meeting the stringent requirements of the pharmaceutical industry. Our product catalog includes:

• Gabapentin API (Active Pharmaceutical Ingredient) reference standard: The purest API raw material form for use as a primary reference standard.
• Pharmacopoeial impurities of Gabapentin: Including impurities listed and controlled according to international pharmacopoeias such as USP, EP, BP.
• Non-pharmacopoeial impurities of Gabapentin: Other impurities that may arise but are not yet officially listed in the pharmacopoeia, still needing to be controlled to ensure product safety.
• Stable isotopes of Gabapentin: Isotopic versions of Gabapentin used in in-depth research, mass spectrometry analysis, and bioavailability testing.

Benefits of choosing our products:

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