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 |
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
