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Home > Active Pharmaceutical Ingredients > Other Chemical Drugs (Find 970 items)

Other Chemical Drugs

Tesofensine

(402856-42-2)

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Hexafluoroacetylacetone

(1522-22-1)
clear colorless to slightly yellow liquidHEXAFLUOROACETYLACETONE acts as a chelating ligand. For example, it can forms metal-chelate complexes with Ca(II), Zn (II), Cu(II), Ni(II), Co(II), Nd(III), Rh(III), Fe(III) and Cr(III), making it be useful in extracting related metal ions. It can also be used as liquid crystal intermediate.

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Ethyl 2-oxocyclopentanecarboxylate

(611-10-9)
Medicinal synthesis, organic synthesis intermediates, can be used to synthesize fragrances, or loxosol.

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Ethyl 3-ethoxypropionate

(763-69-9)
Used as solvent in preparing new polymers.1,2

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Aloe vera, ext.

(85507-69-3)
aloe vera is an emollient and film-forming gum resin with hydrating, softening, healing, anti-microbial, and anti-inflammatory proper ties. It is most widely recognized for its moisturizing capacity. Aloe vera supplies moisture directly to the skin tissue. other properties include moisture regulation and an apparent ability to absorb uV light. It has a slightly relaxing effect on the skin, making it valuable for sensitive, sunburned, and sun-exposed skins. Aloe vera was popular in traditional me

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Doxercalciferol

(54573-75-0)
Synthetic vitamin D prohormone. A new active Vitamin D analog which inhibits growth of human neuroblastoma.Antihyperparathyroid

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Chemical drugs are a general term for compounds that relieve, prevent, and diagnose diseases, as well as compounds that regulate body functions. The industry producing chemical drugs is the chemical and pharmaceutical industry, including the chemical raw material industry and the chemical preparation industry.

Frequently Asked Questions

What are Other Chemical Drugs and how do they differ from APIs?

Other Chemical Drugs refer to a broad category of non-active pharmaceutical substances used in drug development, formulation, or as excipients. Unlike Active Pharmaceutical Ingredients (APIs), which produce the intended therapeutic effect, Other Chemical Drugs may include intermediates, reagents, solvents, or inactive compounds that support manufacturing processes or enhance drug stability and delivery.

What are common applications of Other Chemical Drugs in the pharmaceutical industry?

Other Chemical Drugs are commonly used as synthesis intermediates, formulation additives, pH adjusters, preservatives, or solubilizing agents in drug manufacturing. They play essential roles in ensuring product consistency, shelf life, and bioavailability. These compounds are also critical in research and development for creating novel drug delivery systems and optimizing production efficiency.

How to ensure the quality and compliance of Other Chemical Drugs?

To ensure quality and regulatory compliance of Other Chemical Drugs, buyers should verify that suppliers adhere to international standards such as ISO, GMP, or ICH guidelines. Request Certificates of Analysis (CoA), Safety Data Sheets (SDS), and documentation of purity testing. Additionally, confirm that the chemical is manufactured in facilities with proper environmental, health, and safety controls to minimize contamination risks.

What factors should be considered when sourcing Other Chemical Drugs from suppliers?

When sourcing Other Chemical Drugs, consider the supplier’s reputation, regulatory certifications, batch-to-batch consistency, technical support capabilities, and logistics reliability. Evaluate their ability to provide scalable quantities without compromising purity or documentation. Transparent communication about raw material sourcing and synthesis methods is also crucial for risk mitigation in pharmaceutical supply chains.

Are Other Chemical Drugs subject to regulatory oversight?

Yes, while not all Other Chemical Drugs are classified as APIs, many are still regulated by agencies such as the FDA, EMA, or PMDA—especially if they impact drug safety, efficacy, or quality. Excipients and processing aids used in final dosage forms must meet pharmacopeial standards (e.g., USP, EP). Always confirm regulatory status based on intended use and regional requirements before procurement.

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