Description

Fursultimine Hydrochloride is a high-purity organic compound of significant interest in advanced pharmaceutical research and development. Its primary value lies in its role as a key intermediate or active pharmaceutical ingredient (API) in the synthesis of specialized therapeutic agents. This product is essential for R&D laboratories, pharmaceutical manufacturers, and fine chemical suppliers targeting the global market for novel drug candidates and high-value chemical synthesis.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel drug candidates, particularly in therapeutic areas requiring complex organic molecules.
• Active Pharmaceutical Ingredient (API) Research: Used in the development and formulation studies for new pharmaceutical products.
• Biochemical Research: Serves as a reagent or standard in biochemical assays and pharmacological studies to investigate biological pathways.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for creating complex, high-value specialty chemicals.
• Reference Standard: Utilized as a certified reference material (CRM) in analytical laboratories for quality control and method validation.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	Fursultimine Hydrochloride
CAS No.	2105-43-3
Molecular Formula	C8H12N2O3S • HCl
Molecular Weight	252.72 g/mol
Synonyms	Fursultiamine Hydrochloride; Thiamine Tetrahydrofurfuryl Disulfide Hydrochloride; TTFD Hydrochloride; Alinamin F; Thiamine 8-(Methyl 6-Acetyldihydrothiocotate) Disulfide Hydrochloride; Vitamin B1 Derivative Hydrochloride; 3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-5-(2-hydroxyethyl)-4-methylthiazolium Chloride Tetrahydrofurfuryl Disulfide
EINECS	Contact for details

Quality Control

Our Fursultimine Hydrochloride is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We adhere to relevant industry standards for pharmaceutical intermediates. Comprehensive testing, including identification, assay, and impurity profiling, is performed using validated analytical methods such as HPLC and IR spectroscopy. A Certificate of Analysis (COA) detailing all test results is provided with each shipment to guarantee compliance with your specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.