Tadalafil

Tadalafil

パラメータ 仕様
製品名 Tadalafil
別名 IC351, GF196960
CAS番号 171596-29-5
分子式 C22H19N3O4
分子量 389.4 g/mol
外観 白色からオフホワイトの結晶性粉末
分析(HPLC) ≥99.0%
溶解度 Sparingly soluble in DMSO, practically insoluble in water
パッケージ 25 kg fiber drum, double polyethylene bags inside

Tadalafil Structure

同義語: Tadalafil, 171596-29-5, IC351, GF196960, (6R,12aR)-6-(1,3-Benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1′,2′:1,6]pyrido[3,4-b]indole-1,4-dione

Tadalafil is a synthetic phosphodiesterase type 5 (PDE5) inhibitor developed for the treatment of erectile dysfunction and pulmonary arterial hypertension. It is a chiral, white to off-white crystalline powder with a molecular formula of C22H19N3O4 and a molecular weight of 389.4 g/mol. Unlike other PDE5 inhibitors, tadalafil has a longer half-life and a broader tissue distribution, making it a preferred choice for both on-demand and chronic therapy.

Chemically, tadalafil belongs to the pyrazino[1′,2′:1,6]pyrido[3,4-b]indole class. Its structure features a methylenedioxyphenyl group and a piperazinedione core, which confer high selectivity for PDE5 over other phosphodiesterases. This selectivity underpins its efficacy and favorable side-effect profile. The compound is practically insoluble in water but soluble in organic solvents such as DMSO and dimethylformamide.

Manufactured under cGMP conditions, tadalafil is available at high purity (≥99.0% by HPLC). It is primarily supplied to pharmaceutical companies for the production of finished dosage forms, including tablets for erectile dysfunction and pulmonary arterial hypertension. Our material is routinely tested for identity, assay, and impurities to meet global pharmacopeial standards.

Function & Mechanism

  • PDE5 inhibition: Tadalafil selectively inhibits phosphodiesterase type 5, increasing cyclic guanosine monophosphate (cGMP) levels in smooth muscle cells.
  • Vasodilation: Elevated cGMP promotes relaxation of vascular smooth muscle, enhancing blood flow to the corpus cavernosum and pulmonary arteries.
  • Prolonged action: With a half-life of approximately 17.5 hours, tadalafil provides a longer duration of effect compared to other PDE5 inhibitors.
  • Selectivity: Minimal inhibition of PDE6 and PDE11 reduces the risk of visual disturbances and musculoskeletal side effects.

Source & Standardization

  • 出典: Chemically synthesized via a multi-step chiral process.
  • Standardization: ≥99.0% assay (HPLC), with strict control of chiral purity and related substances.
  • Forms: White to off-white crystalline powder.
  • 用途: Pharmaceutical manufacturing of tablets for erectile dysfunction and pulmonary arterial hypertension; research use.

Quality Specifications (QC Tests)

Test Item 仕様
識別 IR and HPLC retention time match reference standard
乾燥減量 ≤0.5%
焼失残渣 ≤0.11 TP3T
重金属 ≤20 ppm
Organic Impurities Any individual ≤0.1%, total ≤0.5%
残留溶剤 Meets ICH Q3C requirements
Microbial Limits Total aerobic count ≤1000 CFU/g, yeast and mold ≤100 CFU/g

Bulk Supply & Documentation

  • 月間処理能力: 500 kg
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA、MSDS、TDSはご要望に応じてご提供いたします。.
  • パッケージ: 25 kg fiber drum with double polyethylene bags inside.

よくある質問

What is the minimum order quantity (MOQ) for Tadalafil?

Our standard MOQ is 1 kg. For larger quantities, please contact our sales team for pricing and availability.

How long does delivery take?

For stock items, delivery is typically 3-5 business days after order confirmation. We ship globally via express or air freight.

Do you provide a Certificate of Analysis (COA) and samples?

Yes, a COA is available for each batch. Samples can be provided upon request for evaluation purposes.

Contact & Ordering Information

  • Company: LyvBio Co., Ltd.
  • Address: Room 5-0203, Courtyard 205, Lianhu District, Xi’an, Shaanxi, China
  • Email: info@lyvbio.com
  • Phone: +86-29-65816888

send us your specification for a quotation.

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