Naproxen
| 매개변수 | 사양 |
|---|---|
| 제품명 | Naproxen |
| CAS 번호 | 22204-53-1 |
| 분자식 | C14H14O3 |
| 분자량 | 230.26 g/mol |
| 외관 | 흰색에서 미백색의 결정성 분말 |
| 분석법 (HPLC) | 99.0% – 101.0% (on dried basis) |
| 용해도 | Practically insoluble in water; soluble in ethanol, methanol, acetone |
| 패키지 | 25 kg fiber drum with double polyethylene liner |
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동의어: (+)-2-(6-Methoxy-2-naphthyl)propionic acid, (S)-Naproxen, Naprosyn, Aleve, Anaprox, Naprelan, (S)-6-Methoxy-α-methyl-2-naphthaleneacetic acid
Naproxen is a widely prescribed nonsteroidal anti-inflammatory drug (NSAID) of the propionic acid class, valued by formulators for its potent analgesic, antipyretic, and anti-inflammatory effects. In the B2B pharmaceutical market, demand for high-purity naproxen remains strong across generic solid dosage, topical gels, and veterinary preparations, driven by its established efficacy and favorable safety profile compared to other NSAIDs.
Chemically, naproxen is the (S)-enantiomer of 2-(6-methoxy-2-naphthyl)propionic acid, with a molecular formula of C14H14O3 and a molecular weight of 230.26 g/mol. It is practically insoluble in water but freely soluble in common organic solvents such as ethanol and acetone, making it suitable for a range of formulation processes. The compound is typically produced via synthetic routes that ensure high enantiomeric purity, which is critical for its pharmacological activity.
LyvBio supplies naproxen with an assay of 99.0%–101.0% (HPLC, on dried basis), meeting pharmacopeial standards including USP and EP. Each batch is tested for identity, impurities, residual solvents, and heavy metals to ensure compliance with regulatory requirements. Our material is manufactured under cGMP conditions, with full documentation support for ANDA, NDA, and other regulatory submissions.
Naproxen is a single active pharmaceutical ingredient (API) supplied as a white to off-white crystalline powder. It contains no excipients or carriers, ensuring consistent potency and purity for downstream processing. The product is available in various particle sizes to accommodate different formulation needs, from direct compression to wet granulation.
| Test Item | 사양 |
|---|---|
| 식별 | IR and HPLC retention time match reference standard |
| 건조 손실 | ≤ 0.5% |
| 중금속 | ≤ 20 ppm |
| Organic Impurities | Meets USP/EP limits |
| 잔류 용매 | Meets ICH Q3C guidelines |
| Microbial Limits | Total aerobic count ≤ 1000 CFU/g; absence of specified pathogens |
Our standard MOQ is 5 kg. For smaller quantities, please contact our sales team to discuss your specific needs.
For stock items, the lead time is 3-5 business days from order confirmation. We maintain sufficient inventory to ensure prompt shipment.
Yes, a COA is available for each batch. We can also provide samples for evaluation purposes; please specify your requirements when contacting us.
send us your specification for a quotation.