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Shandong Jiulong Hisince Pharmaceutical Co.,Ltd.

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Shandong Jiulong Hisince Pharmaceutical Co.,Ltd.

Country: China (Mainland)

Business Type:Manufacturers

Mr.Richard Bai

Tel: +86-15853188990

Ms.Betty Xue

Tel: +86-13255689879

Ms.Sindy Zhang

Tel: +86-13706449112

Mr.Richard

Tel: 0531-69953158

Ms.Essence Sun

Tel: +86-16653124667

Mobile: 008615853188990

Tel: +86-15853188990

Fax:

Province/state: Shandong

City: Jinan

Street: Huadian Pioneer Park, Huadian Township, Qihe County, Dezhou City, Shandong, P.R.China

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Tadalafil CAD No.:171596-29-5

CAS NO.171596-29-5

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T
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Product Details

Keywords

  • Tadalafil CAD No.:171596-29-5
  • 171596-29-5
  • Tadalafil CAD No.:171596-29-5

Quick Details

  • ProName: Tadalafil CAD No.:171596-29-5
  • CasNo: 171596-29-5
  • Appearance: white
  • Application: API
  • DeliveryTime: prompt
  • PackAge: durm
  • Port: shanghai
  • ProductionCapacity: 1000 Kilogram/Month
  • Purity: 99.5%
  • Storage: cool and dryer
  • Transportation: by sea ar by air
  • LimitNum: 1 Kilogram
  • Valid Period: 2 years

Superiority

Tadalafil Citrate

Alias: Tadalafei;Cialis

CAS No: 171596-29-5

MF: C22H19N3O4

MW: 389.41

Purity: 99.5%

Appearance: white powder, odorless, tasteless, insoluble in water and alcohol.

Details

Tadalafil Citrate

Alias: Tadalafei;Cialis

CAS No: 171596-29-5

MF: C22H19N3O4

MW: 389.41

Purity: 99.5%

Appearance: white powder, odorless, tasteless, insoluble in water and alcohol.

 

 

Applications:

 

Although sildenafil (Viagra), vardenafil (Levitra), and tadalafil (Cialis) all work by inhibiting PDE5, tadalafil's pharmacologic distinction is its longer half-life (17.50 hours) – compared to sildenafil (4.0–5.0 hours) and vardenafil (4.0–5.0 hours) – resulting in longer duration of action, and so partly responsible for "The Weekend Pill" sobriquet. Furthermore, the longer half-life is the basis for current investigation of tadalafil's daily therapeutic use in relieving pulmonary arterial hypertension. Sildenafil is approved in several world regions as a thrice-daily therapy for pulmonary arterial hypertension.

 

 

Specifications:

 

 

 

Test Items

Specification

Test Results

Appearance

White powder

Conforms

Test method

High pressure liquid chromatography(HPLC)

Conforms

Melting Point

300℃~303℃

301.5℃-302.6℃

Loss on drying

≤0.5%

0.24%

Heavy metals(Pb)

≤20ppm

7.5ppm

Residue on ignition

≤0.1%

0.08%

Relative substance

≤1.0%

0.145%

Assay (on dried basis)

≥98.5%

99.33%

Conclusion

The product conform to USP 32.

 

 

ATT:

and for transport, we have professional transport team to operate,so for delivery, high customs passing rate.

 

3. Safe and fast delivery

 

4. good after-sales service