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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
Twenty years of qualification
Audited Supplier
Pharma Sources Insight June 2024: Globalization on the Go
