Anthralin USP

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Anthralin USP Specification

Moisture (%)
0.20%

Smell
Characteristic

Assay
99.0% - 101.0%

HS Code
29209090

EINECS No
214-626-7

Heavy Metal (%)
0.002%

Loss on Drying
0.5%

Structural Formula
C14H10O3

Taste
Bitter

Water Solubility
Practically insoluble

Molecular Weight
226.23 g/mol

Grade
USP Grade

Ph Level
Neutral

Shelf Life
5 years

Molecular Formula
C14H10O3

Storage
Keep tightly closed in a cool, dry place

Chemical Name
Anthralin USP

CAS No
1143-38-0

Usage
Pharmaceutical raw material, used in treatment of psoriasis

Purity(%)
99.0% minimum

Appearance
Yellow-brown crystalline powder

Application
Used for external application for skin disorders

About Anthralin USP

Anthralin USP

CAS No.: 1143-38-0

Molecular Formula : C14H10O3

Molecular Weight : 226.23

Appearance : Lemon yellow leaflets or plates

Melting Point : 17°C

Water Solubility : <0.1 g/100 mL at20

Assay : 98.5%-101%

Specs : As per BP 2005/EP 2004

Uses : Antipsoriatic

Pharmaceutical-Grade Quality

Anthralin USP meets stringent United States Pharmacopeia (USP) criteria, ensuring high purity (99.0101.0%) and minimal impurities (0.10%). Each batch is meticulously identified using IR, HPLC, and TLC, guaranteeing conformity to international standards for pharmaceutical applications.

Optimized Stability and Shelf Life

This product remains stable for up to five years if correctly stored in a tightly closed container, away from excessive moisture and heat. Its physical characteristicssuch as a neutral pH and low moisture contentfurther optimize preservation over time, making it highly reliable in pharmaceutical environments.

Safe and Practical Packaging

Anthralin USP is offered in HDPE or glass bottles and drums, available in various sizes to accommodate different operational needs. The product is non-hazardous and unregulated for transport, ensuring safety and compliance for distributors and manufacturers globally.

FAQs of Anthralin USP:

Q: How is Anthralin USP typically used in pharmaceutical applications?

A: Anthralin USP is widely used as a raw material in the external treatment of skin disorders, especially psoriasis. It is formulated into creams or ointments for topical application by healthcare professionals or pharmaceutical manufacturers.

Q: What are the recommended storage and handling practices for Anthralin USP?

A: Store Anthralin USP tightly closed in a cool, dry place to maintain stability and avoid moisture contamination. It is stable under these recommended conditions and has a shelf life of up to five years.

Q: When should Anthralin USP be used in the formulation process?

A: Anthralin USP should be incorporated during the preparation of topical formulations for treating specific skin conditions like psoriasis, as directed by formulators and according to standard pharmaceutical guidelines.

Q: Where can distributors or manufacturers source Anthralin USP?

A: Anthralin USP can be sourced from recognized pharmaceutical distributors, exporters, importers, manufacturers, suppliers, traders, and wholesalers, especially within India and global markets that require USP-grade excipients.

Q: What is the benefit of using micronized Anthralin USP?

A: Micronized grades of Anthralin USP offer enhanced dispersion and absorption in topical formulations, improving therapeutic efficacy and uniform application on the skin.

Q: How is Anthralin USP identified according to quality standards?

A: Identification is performed through advanced analytical techniques such as Infrared Spectroscopy (IR), High-Performance Liquid Chromatography (HPLC), and Thin Layer Chromatography (TLC) following USP protocols.

Q: What safety and transport considerations apply to Anthralin USP?

A: Classified as non-hazardous and not regulated for transport, Anthralin USP can be shipped safely in HDPE or glass containers without requiring special handling or regulatory documentation.

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