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Home > Products >  Lower price Travoprost

Lower price Travoprost CAS NO.157283-68-6

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  • FOB Price: USD: 220.00-230.00 /Gram Get Latest Price
  • Min.Order: 0 Metric Ton
  • Payment Terms: L/C,T/T
  • Available Specifications:

    99%+(1-10)Gram99%+(10-100)Gram

  • Product Details

Keywords

  • Travoprost
  • Manufacture
  • Prostaglandins

Quick Details

  • ProName: Lower price Travoprost
  • CasNo: 157283-68-6
  • Molecular Formula: C26H35F3O6
  • Appearance: pale yellow Oil
  • Application: eye drops, anti-glaucoma
  • DeliveryTime: within 2 days
  • PackAge: 1g/package, 5g/package, 10g/package, 1...
  • Port: Pudong,Shanghai, China
  • ProductionCapacity: 200 Gram/Month
  • Purity: 98.5%
  • Storage: Store in dry, dark and ventilated plac...
  • Transportation: room temperature
  • LimitNum: 0 Metric Ton
  • Related Substances: ≤ 0.50%
  • Residue on Ignition: ≤ 0.50%
  • Heavy Metal: ≤ 10ppm
  • Valid Period: 2years store a temperature below -15℃

Superiority

Tests

Specifications

Results

Appearance

Colorless to yellowish viscous oily liquid

Yellowish viscous oily liquid

Identification

 

By TLC

The Travoprost should be appear as Black Spots.

Conforms

By HPLC

The Retention time of the maior peak in the chromatogram of the test preparation corresponding to that in the chromatogram of the standard preparation, as per Assay test.

Conforms

Specific Rotation

[α]20D: +52.0° ~ +58.0°at 365nm

55.3°

Water

N.M.T.1.0 %

0.2%

Limit of ethyl acetate

N.M.T. 5000ppm

1400ppm

Travoprost Related compound A

N.M.T. 0.2%

N.D.

15-epi Diasteromer

N.M.T. 0.5%

0.18%

5,6-trans Isomer

N.M.T. 3.5%

0.80%

15-Keto derivative

N.M.T. 0.3%

N.D.

Any other impurity

N.M.T. 0.1%

0.09%

Total impurities

N.M.T. 4.0%

1.2%

Assay: Travoprost

96.0% ~ 102%(C26H35F3O6)

98.4%

Conclusion

Conform to USP37

 

 

Details

our quality system

we has a sound quality management system and documents, equipped with shimadzu hplc, gc chromatography and other series of testing equipment, in order to meet the quality priority principle. quality management department is independent of the production system, and execute with quality inspection and quality supervision, quality management functions.

the qa department is responsible for establishing and perfecting the quality supervision system, and set up the qa personnel from supplier evaluation of material, raw material procurement, warehousing acceptance, production, release, sales, customer feedback to monitor the whole process, further standardize and improve the quality management system; at the same time, we do on-site inspection and regular quality report and other means to manage the quality system, and regularly organize gmp training to update employee’s knowledge and improve the quality concept. we are strictly implementing gmp management, and are open to accept external customer audit and official inspections.

our r & d

we use the advantage of combination of chemical synthesis and purification technology platform, to carry out research and development of various apis and intermediates with high degree of difficulty, especially chiral drugs.

our r & d team has more than 5 year-experience in r & d and scale production of prostaglandins, anti-cancer drugs and hypoglycemic drugs. all of these products have achieved commercial production, and occupied a leading position in the market competition. 

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