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Ethinyl Estradio API

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MOQ : 25 Kilograms

Ethinyl Estradio API Specification

Loss on Drying
0.5%

HS Code
29372300

Solubility
Slightly soluble in water; soluble in alcohol, chloroform, and acetone

Molecular Formula
C20H24O2

Structural Formula
C20H24O2

Color
White to off-white

Storage
Store in a cool, dry place. Protect from light and moisture.

EINECS No
200-342-2

Molecular Weight
296.40 g/mol

Particle Size
Micronized, 90% < 20 microns

Melting Point
182-185 C

Heavy Metal (%)
0.001%

Shelf Life
36 months

Poisonous
No (when used as directed)

Boiling point
Not Applicable (decomposes)

Smell
Odorless

Medicine Name
Ethinyl Estradiol API

Chemical Name
Ethinyl estradiol

CAS No
57-63-6

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Used in hormonal contraceptives and hormone replacement therapy

Purity(%)
>99%

Appearance
White to off-white crystalline powder

Physical Form
Solid

Related Substances
Each impurity 0.5%, total impurities 1.0%

Residue on Ignition
0.1%

Assay (HPLC)
>99.0%

Microbial Limits
Total aerobic microbial count < 1000 CFU/g, total yeast & mould < 100 CFU/g

Specific Optical Rotation
+75 to +80 (in ethanol)

Packaging
Bottle or drum, according to customer requirements

Identification
Complies with standard by IR and UV tests

Ethinyl Estradio API Trade Information

Minimum Order Quantity
25 Kilograms

Payment Terms
Cash on Delivery (COD), Cash in Advance (CID), Cash Against Delivery (CAD)

Supply Ability
500 Kilograms Per Month

Delivery Time
5-7 Days

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India

About Ethinyl Estradio API

Ethinyl Estradiol API is an acclaimed, select Active Pharmaceutical Ingredient (API) renowned for its formidable purity, boasting an assay of >99.0% and reduced levels of residual impurities. Presented as a white to off-white crystalline powder, this pharmaceutical-grade compound is optimized for use in hormonal contraceptives and hormone replacement therapies. Manufactured to comply with towering global standards by rigorous IR and UV identification, its optimum particle size ensures efficacy in formulation. Ethinyl Estradiol is supplied in customized packaging-bottles or drums-matching diverse client needs, while its stability and safety are maintained through reduced heavy metal content and stringent microbial limits.

Key Features & Application Method of Ethinyl Estradiol API

Ethinyl Estradiol API is applied as a foundational component in the formulation of hormonal contraceptives and hormone replacement therapies. Its optimum micronized particle size-90% under 20 microns-ensures rapid and uniform blending, enabling superior bioavailability. The crystalline powder is suitable for oral solid dosage forms and must be integrated by pharmaceutical professionals in controlled environments. The surface of application is primarily within tablet and capsule matrices, guaranteeing optimum absorption and efficacy.

Global Markets, Certifications, and Swift Delivery for Ethinyl Estradiol API

Ethinyl Estradiol API is supplied to formidable main export markets across Europe, Asia, and the Americas, supported by rigorous certifications and compliance protocols. Shipments are meticulously packaged according to proposal amounts and customer specifications in either bottles or drums. Delivery times are optimized for prompt international distribution, ensuring the product arrives with uncompromised quality. The API holds recognized certifications that reinforce its reliability in global pharmaceutical supply chains.

FAQ's of Ethinyl Estradio API:

Q: How is Ethinyl Estradiol API typically used in pharmaceutical formulations?

A: Ethinyl Estradiol API is primarily used as a critical hormonal agent in the development of oral contraceptives and hormone replacement therapy preparations, ensuring desired therapeutic effects.

Q: What testing protocols are followed for the identification and purity of Ethinyl Estradiol API?

A: The API is assessed using IR and UV tests for identification, while its purity is confirmed by HPLC assay (>99.0%) and strict monitoring of related substances and heavy metal content.

Q: Where is the surface of application for Ethinyl Estradiol API?

A: The surface of application is within pharmaceutical dosage forms such as tablets and capsules, where the API is uniformly blended to ensure optimum bioavailability.

Q: When can I expect delivery after placing a shipment order for Ethinyl Estradiol API?

A: Delivery times depend on the destination and shipment size but are generally optimized for rapid fulfillment. Most orders are dispatched within the proposed timeframe agreed during order confirmation.

Q: What benefits does the reduced impurity profile of Ethinyl Estradiol API offer?

A: The lowered impurity content enhances product safety, stability, and compliance with global regulatory standards, ultimately improving patient confidence and therapeutic outcomes.

Q: How should Ethinyl Estradiol API be stored to maintain its optimum quality?

A: The API should be stored in a cool, dry place, protected from light and moisture, in tightly sealed original packaging to ensure a maximum shelf life of 36 months.

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