Dobutamine HCL Cas No.49745-95-1
Product Source: Synthetic
Specification: ≥98.5%
CAS No.: 49745-95-1
Molecular Formula: C₁₈H₂₄ClNO₃
Molecular Weight: 337.85 g/mol
Testing Method: HPLC
Active Ingredient: Dobutamine Hydrochloride
Product Characteristics: White or off-white crystalline powder, odorless or with slight characteristic odor
Product Packaging: 1kg/bag; 25kg/drum
Storage Conditions: Store in a cool, dry place, protected from light and sealed
Shelf Life: 24 months
Declaration of Use: This product is intended for industrial use or scientific research only.
Dobutamine Hydrochloride API (Pharmaceutical Grade)
CAS No: 49745-95-1 | ≥98.0% Purity | USP/EP/ChP Compliant
1. Product Description
Dobutamine Hydrochloride is a synthetic catecholamine used as a selective β₁-adrenergic agonist. It is a critical active pharmaceutical ingredient (API) utilized in the formulation of sterile parenteral (injectable) products. Xi'an Tihealth manufactures this compound under strict GMP conditions to ensure high molecular integrity and low impurity profiles, suitable for the treatment of acute heart failure and cardiovascular resuscitation.
2. Technical Specifications (COA Data)
| Parameter | Specification |
|---|---|
| Assay (Dried Basis) | 98.0% - 102.0% |
| Identification (IR/HPLC) | Conforms to Standard |
| Loss on Drying | ≤ 1.0% |
| Heavy Metals (Pb/As/Cd/Hg) | ≤ 10 ppm total |
| Related Substances | Complies with USP/EP Monograph |
| Bacterial Endotoxins | Tested for Sterile Injectable Application |
3. Packaging & Storage
To ensure maximum stability and prevent oxidative degradation, we provide:
- Packaging: 25kg/fiber drum with double PE inner bags, or customized sterile-grade aluminum foil vacuum packaging.
- Storage: Store in a light-resistant, airtight container. Keep in a cool, dry place (25°C recommended).
- Shelf Life: 24 months from the date of manufacture under specified conditions.
4. Regulatory & Supply Chain Support
Xi'an Tihealth is committed to providing full regulatory support for pharmaceutical manufacturing:
- Documentation: Full COA, MSDS, TDS, and Method of Analysis (MOA) provided per batch.
- Quality System: Manufacturing under strict GMP quality management; audit support available for long-term partners.
- Technical Support: Our team assists with impurity profile documentation and regulatory DMF file alignment for finished drug registration.
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