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D-Cysteine API Manufacturers & Suppliers

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D-Cysteine | CAS No: 921-01-7 | GMP-certified suppliers

A medication that serves as an experimental amino acid derivative for research in redox biology and protein structure stabilization without established therapeutic uses.

Generic name
D-Cysteine
Molecule type
small molecule
CAS number
921-01-7
DrugBank ID
DB03201
Approval status
Experimental drug

Product Snapshot

  • D-Cysteine is an oral small molecule intermediate used in pharmaceutical formulations
  • Its primary applications include research and development in metabolic and enzymatic studies
  • It is currently classified as experimental with no established regulatory approvals

Clinical Overview

D-Cysteine (CAS Number 921-01-7) is a thiol-containing non-essential amino acid structurally related to the more commonly occurring L-cysteine. It is characterized by the presence of a sulfhydryl group, which contributes to its chemical reactivity, particularly its oxidation to form cystine via disulfide bond formation. This molecular transformation plays a role in redox biology and protein structure stabilization in broader biochemical contexts, although specific clinical indications or pharmacological uses of D-cysteine have not been established.

D-Cysteine belongs to the class of organic compounds known as cysteine and derivatives. These compounds include molecules derived through modification of the cysteine amino or carboxy groups or by substitution of hydrogen atoms within the glycine residue with heteroatoms. The stereochemical configuration of D-cysteine differentiates it from the L-enantiomer, with implications for its biological recognition and metabolism.

Currently, D-cysteine is categorized as experimental, with no approved therapeutic applications or formally recognized pharmacodynamics and mechanisms of action. As such, it is primarily utilized in research settings to explore biochemical pathways involving thiol chemistry, amino acid metabolism, and potential roles in enzyme function or redox balancing.

Key ADME parameters for D-cysteine are not well characterized in the literature. However, general metabolic understanding of amino acids suggests potential rapid absorption, distribution predominantly through systemic circulation, oxidation to cystine, and renal excretion of metabolites. Safety and toxicity data are limited; nevertheless, as with many amino acid derivatives, considerations include possible effects on sulfur metabolism and reactivity with cellular nucleophiles. No significant safety signals or toxicological profiles have been documented in clinical contexts due to its experimental status.

D-cysteine is not associated with any marketed pharmaceutical products or branded formulations. Its application remains within investigational and academic research domains rather than clinical or commercial pharmaceutical development.

From a sourcing perspective, quality considerations for D-cysteine as an active pharmaceutical ingredient (API) focus on stereochemical purity, control of residual impurities, and stability, given the susceptibility of thiol groups to oxidation. Reliable suppliers should provide documentation confirming enantiomeric excess and compliance with relevant pharmacopeial standards or established analytical methods. Appropriate storage and handling protocols must be maintained to preserve API integrity for research or formulation purposes.

Identification & chemistry

Generic name D-Cysteine
Molecule type Small molecule
CAS 921-01-7
UNII IU8WN3PPI2
DrugBank ID DB03201

Pharmacology

Targets
TargetOrganismActions
Carboxypeptidase A1Humans

Formulation & handling

  • D-Cysteine is a small molecule compound suitable for oral formulation due to its high water solubility.
  • Its low LogP value indicates high polarity, which may affect membrane permeability and absorption.
  • Handling should consider its sensitivity to oxidation, requiring protection from air and light during storage.

Regulatory status

D-Cysteine is a type of Other substances


The pharmaceutical industry encompasses a diverse range of active pharmaceutical ingredients (APIs) that are used in the production of various medications. One category of APIs is known as other substances. This category includes substances that do not fall under the conventional classifications such as antibiotics, analgesics, or antihypertensives.

Other substances in pharmaceutical APIs consist of a broad array of chemical compounds with unique properties and applications. These substances play a crucial role in the formulation and development of specialized medications, catering to specific therapeutic needs. The category encompasses various substances like excipients, solvents, stabilizers, and pH adjusters.

Excipients are inert substances that aid in the manufacturing process and enhance the stability, bioavailability, and patient acceptability of pharmaceutical formulations. Solvents are used to dissolve other ingredients and facilitate their incorporation into the final product. Stabilizers ensure the integrity and shelf life of medications by preventing degradation or chemical changes. pH adjusters help maintain the desired pH level of a formulation, which can influence the drug's efficacy and stability.

Pharmaceutical manufacturers carefully select and incorporate specific other substances into their formulations, adhering to regulatory guidelines and quality standards. These substances undergo rigorous testing and evaluation to ensure their safety, efficacy, and compatibility with the desired pharmaceutical product. By employing other substances in API formulations, pharmaceutical companies can optimize drug delivery, improve patient compliance, and enhance therapeutic outcomes.

In summary, the other substances category of pharmaceutical APIs comprises a diverse range of chemicals, including excipients, solvents, stabilizers, and pH adjusters. These substances contribute to the formulation, stability, and performance of medications, enabling pharmaceutical manufacturers to develop specialized products that meet specific therapeutic requirements.

D-Cysteine API manufacturers & distributors

Compare qualified D-Cysteine API suppliers worldwide. We currently have 1 companies offering D-Cysteine API, with manufacturing taking place in 1 different countries. Use the table below to review supplier type, countries of origin, certifications, product portfolio and GMP audit availability.

SupplierTypeCountryProduct originCertificationsPortfolio
Producer
China China CoA32 products

When sending a request, specify which D-Cysteine API quality you need: for example EP (Ph. Eur.), USP, JP, BP, or another pharmacopoeial standard, as well as the required grade (base, salt, micronised, specific purity, etc.).

Use the list above to find high-quality D-Cysteine API suppliers. For example, you can select GMP, FDA or ISO certified suppliers. Visit our help page to learn more about sourcing APIs via Pharmaoffer.