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Buformin Hydrochloride CAS NO 1190-53-0
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CAS No.:1190-53-0
Grade:Pharmacy Grade
Content:99.0%
Brand:Customizable
Packaging:Customizable
Description
Buformin Hydrochloride is a high-purity pharmaceutical active ingredient belonging to the biguanide class of compounds. It is a critical intermediate and reference standard for research and development in metabolic and endocrine disorders. This compound is essential for pharmaceutical manufacturers, research institutions, and analytical laboratories focused on diabetes research and drug development. Our supply ensures consistent quality and reliable availability for global B2B partners.
Application
- Pharmaceutical Active Ingredient (API): Primary use as the active pharmaceutical substance in the formulation of antidiabetic medications.
- Reference Standard: Serves as a certified reference material (CRM) for quality control and analytical method validation in pharmaceutical testing laboratories.
- Biochemical Research: Used in metabolic studies to investigate mechanisms of action related to glucose metabolism and insulin sensitivity.
- Preclinical & Clinical Research: Employed as a key material in the development and testing of new therapeutic agents for type 2 diabetes.
- Chemical Synthesis Intermediate: Acts as a crucial building block for the synthesis of novel biguanide derivatives and related compounds.
Basic Information
| Product Name | Buformin Hydrochloride |
| CAS No. | 1190-53-0 |
| Molecular Formula | C6H15N5•HCl |
| Molecular Weight | 209.68 g/mol |
| Synonyms | Buformin HCl; 1-Butylbiguanide Hydrochloride; N-Butylbiguanide Hydrochloride; Silubin; Glybigidum; DB 1; DB-1; Buformini Hydrochloridum |
| EINECS | 214-730-6 |
Quality Control
Our Buformin Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and impurity profiles. We support compliance with cGMP and ICH guidelines for API manufacturing.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and prevent degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






