Lamotrigine
| 제품명 | Lamotrigine |
|---|---|
| CAS 번호 | 84057-84-1 |
| 분자식 | C9H7Cl2N5 |
| 분자량 | 256.09 g/mol |
| 외관 | 흰색에서 미백색의 결정성 분말 |
| 분석법 (HPLC) | 98.0% – 102.0% |
| 융점 | 216–218 °C |
| 용해도 | Sparingly soluble in water; soluble in dimethyl sulfoxide, dimethylformamide |
| 패키지 | 25 kg fiber drum with double polyethylene liner |
도움이 필요하신가요? 저희 팀에 문의해 주세요

동의어: 3,5-Diamino-6-(2,3-dichlorophenyl)-1,2,4-triazine, Lamictal, LTG, BW-430C, 6-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5-diamine
Lamotrigine is a phenyltriazine derivative that has carved out a distinct place in the anticonvulsant and mood-stabilizer markets since its approval in the 1990s. Unlike older antiepileptics that emerged from serendipitous screening, lamotrigine was designed to inhibit glutamate release—a mechanism that translates into broad-spectrum efficacy across partial and generalized seizures. For procurement teams, it represents a reliable, well-characterized API with steady demand from both generic and branded formulators.
From a chemical standpoint, lamotrigine is a small molecule (C9H7Cl2N5) with a dichlorophenyl ring attached to a diaminotriazine core. This structure gives it moderate lipophilicity and a low aqueous solubility, which formulators often address through salt formation or particle-size engineering. The compound is chemically stable under normal storage conditions, though it is light-sensitive and should be protected from prolonged exposure to strong UV light.
Manufacturing lamotrigine at commercial scale typically involves a multi-step synthesis starting from 2,3-dichlorobenzoyl chloride or related precursors. The critical quality attributes—assay, related substances, and residual solvents—are tightly controlled to meet pharmacopeial monographs (USP, EP, BP). Our material is produced under cGMP conditions and is available with full regulatory support, including DMF and CEP where applicable.
While lamotrigine is best known for epilepsy, its use in bipolar disorder—particularly for delaying depressive episodes—has expanded its clinical footprint. This dual indication keeps demand stable across multiple therapeutic categories, making it a strategic API for companies serving both neurology and psychiatry markets.
| 매개변수 | 사양 |
|---|---|
| Assay (HPLC, dried basis) | 98.0% – 102.0% |
| 식별 | IR, UV conforms to reference standard |
| 건조 손실 | ≤ 0.5% |
| 소각 잔류물 | ≤ 0.1% |
| 중금속 | ≤ 20 ppm |
| 관련 물질 | Total impurities ≤ 0.5%; each unspecified ≤ 0.1% |
| 잔류 용매 | Meets USP / EP 5.4 requirements |