Tadalafil

Tadalafil

매개변수 사양
제품명 Tadalafil
다른 이름 IC351, GF196960
CAS 번호 171596-29-5
분자식 C22H19N3O4
분자량 389.4 g/mol
외관 흰색에서 미백색의 결정성 분말
분석법 (HPLC) ≥99.0%
용해도 Sparingly soluble in DMSO, practically insoluble in water
패키지 25 kg fiber drum, double polyethylene bags inside

도움이 필요하신가요? 저희 팀에 문의해 주세요

Tadalafil Structure

동의어: 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

  • Source: 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.
  • 응용 분야: Pharmaceutical manufacturing of tablets for erectile dysfunction and pulmonary arterial hypertension; research use.

Quality Specifications (QC Tests)

Test Item 사양
식별 IR and HPLC retention time match reference standard
건조 손실 ≤0.5%
소각 잔류물 ≤0.1%
중금속 ≤20 ppm
Organic Impurities Any individual ≤0.1%, total ≤0.5%
잔류 용매 Meets ICH Q3C requirements
Microbial Limits Total aerobic count ≤1000 CFU/g, yeast and mold ≤100 CFU/g

Bulk Supply & Documentation

  • Monthly capacity: 500 kg
  • 리드 타임: 3-5 business days (stock items)
  • 문서: COA, MSDS, TDS available upon request.
  • 포장: 25 kg fiber drum with double polyethylene bags inside.

자주 묻는 질문

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.

연락 유지

견적 요청

주소

Room,5-0203, Unit 5, Beiyuanmen Street,Xi'an,Shaanxi,China

✅ ×