High Quality Dinoprost Powder CAS 551-11-1

Product Details
Customization: Available
Powder: Yes
Customized: Customized
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10000000 RMB
Plant Area
101~500 square meters
  • High Quality Dinoprost Powder CAS 551-11-1
  • High Quality Dinoprost Powder CAS 551-11-1
  • High Quality Dinoprost Powder CAS 551-11-1
  • High Quality Dinoprost Powder CAS 551-11-1
  • High Quality Dinoprost Powder CAS 551-11-1
  • High Quality Dinoprost Powder CAS 551-11-1
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Basic Info.

Model NO.
Dinoprost
Certification
GMP, ISO 9001, USP, BP
State
White to off-White Crystalline
Purity
>99%
CAS
551-11-1
Mf
C20h34o5
MW
354.48
Shelf Life
24 Months
Storage
Cool Dry Place
Transport Package
1kg/Bag, 25kg/Drum
Specification
Dinoprost
Trademark
HNB
Origin
China
Production Capacity
2000kg/Month

Product Description

High Quality Dinoprost Powder CAS 551-11-1
Product name Dinoprost
Cas number 551-11-1
Molecular formula C20H34O5
Molecular weight  354.48
Appearance White to off-white crystalline solid
Melting point 25-35ºC
Boiling point 531ºC at 760 mmHg
Relative density 1.153 g/cm3


Indications

Induced abortion in the second trimester of pregnancy (16 weeks to 20 weeks) and expired abortion, fetal death or congenital malformation of the fetus can also be used for induction of labor during term pregnancy and for angiography.

Pharmacokinetics

Absorption after amniocentesis, slowly entering the systemic circulation, the average abortion takes 20h ~ 24h, T1/2 in amniotic fluid is 3h ~ 6h, T1/2 is shorter than 1min in intravenous injection. Degraded in the lungs and liver, metabolites are mainly excreted from the kidneys.
 

High Quality Dinoprost Powder CAS 551-11-1

High Quality Dinoprost Powder CAS 551-11-1

Item

Standard

Structural data confirmation

1. H-NMR: The data of structure are identical with reference standard

2. HPLC-MS: Ensure the molecular weight of main peak and fragment peak are identical with reference standard

3. IR:The data of IR are identical with that of reference standard

Purity(HPLC)

≥99.0%

Related impurities

Specific single impurity

Meets EP/USP/BP standards

Non-specific single impurity

≤0.10%

Total Impurities

≤0.50%

Crystal form

Meets EP/USP/BP standards

Loss on drying

1.0%

Water

≤1.0%

Inorganic salt

≤0.1%

Heavy metals

≤10 ppm

Assay

99.0%~101.0%(According to EP/USP/BP standards)

Microbiological Analysis

Total plate count

≤1000cfu/g

Yeast and Moulds

≤100cfu/g

E. Coli.

Absent

Salmonella

Absent

S.aureus

Absent


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