99% up by HPLC GMP DMF DL-Cloprostenol Sodium 55028-72-3

Grade: Pharmaceutical Grade

Factory Location: Xiamen, Fujian

Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East

Sample Provided: yes

Payment Terms: L/L

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