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Postion:Product Catalog >API>Hormones and the Endocrine System>Prostaglandin drugs>DL-Cloprostenol Sodium
DL-Cloprostenol Sodium
  • DL-Cloprostenol Sodium
  • DL-Cloprostenol Sodium
  • DL-Cloprostenol Sodium
  • DL-Cloprostenol Sodium
  • DL-Cloprostenol Sodium

DL-Cloprostenol Sodium

Price Get Latest Price
Package 25KG
Min. Order: 2KG
Supply Ability: 20 tons
Update Time: 2024-04-22

Product Details

Product Name: DL-Cloprostenol Sodium CAS No.: 55028-72-3
Min. Order: 2KG Purity: 98% up, GMP, DMF
Supply Ability: 20 tons Release date: 2024/04/22

Product Information

Product name

DL-Cloprostenol Sodium

CAS No.

55028-72-3

Molecular Formula

C22H28Cl NaO6

Molecular Weight

446.9

Quality Standard

98% up, Medicine Grade

Appearance

White amorphous powder

COA of DL-Cloprostenol Sodium

TEST

SPECIFICATION

RESULTS

Appearance

White or almost white amorphous powder

Almost white amorphous powder

Identification

 A. IR



 B. Reaction of sodium salts


The infrared absorption spectrum of the sample is concordant with the reference spectrum of cloprostenol sodium

Yields reaction A characteristic of sodium salts


Conform


Conform

Related substances

  Any unspecified impurity

  Total impurities


≤ 1.0%

≤ 2.5%


0.18%

0.57%

Residual Solvents

  Acetone


≤ 0.5%


0.01%

Water

≤ 3.0%

0.94%

Assay

97.5%-102.5% (on the anhydrous basis)

98.2%

Conclusion

Complies with the BP and in-house standards

Usage

Function of DL-Cloprostenol Sodium

DL-Cloprostenol Sodium is a synthetic prostaglandin F2a homologue. It has strong the function of dissolving luteal; It also can quickly cause corpus luteum regression, and suppress the secretion. It has direct excitation effect on uterine smooth muscle, and cause uterine smooth muscle contraction, cervical relaxation. For sexual cycle normal animals, usually Estrus in 2-5 days after heat treatment.
In pregnancy 10 ~ 150 days pregnant cows, usually during the injection using 2 ~ 3 days after abortion.

Our Advantage of DL-Cloprostenol Sodium

1. Excellent quality: conform to BP standard, with high purity: Any impurity: NMT1.0%, Total impurity: NMT 2.5%; assay 98% up,

2. GMP, DMF available

3. Large capacity & stock : 10 kg/month with 1-2kg in stock for prompt shipment


Article illustration





Company Profile Introduction

Sinoway Industrial co., ltd. was established in 1987 in Xiamen, China, and now has been a leading group specialized in research, development, custom manufacturing and trading of pharmaceutical intermediates, APIs, health and food supplements, cosmetic raw materials, herbal extracts, polypeptides and prostaglandin derivatives, etc.. We have passed ISO9001:2015. With qualified products, competitive price and excellent service, we have received great reputation of our customers from all over the world, including Southeast Asia, Europe, North America, South America, Middle East and other countries. We have over 20 years good partners in Japan、Korea and Switzerland. Sinoway has a professional R&D team. We have built close cooperative relationships with many research institutes and universities in China. Moreover, Sinoway combines market analysis with technology, providing new business trends to our clients. In addition, we have very close cooperation relationships with many Chinese pharmaceutical factories. These pharmaceutical manufacturers have GMP regulated workshops, advanced production and testing equipments, first-class QC labs and a production team with rich experience. We can supply various Active Pharmaceutical Ingredients and finished products which meet EP/USP/BP standards. Chinese GMP, EU-GMP, COS/CEP certificates with DMF documents are available, and many products have been approved by FDA. We believe that quality and innovation are vital for an enterprise. Adhering to the business philosophy of integrity and win-win cooperation, Sinoway is looking forward to have a bright future with you together.

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