Description

Salbupart CAS NO 114101-13-2 is a specialized pharmaceutical intermediate and fine chemical compound. It is a critical building block in the synthesis of advanced active pharmaceutical ingredients (APIs), valued for its specific molecular structure that enables targeted therapeutic effects. This compound is essential for research institutions and manufacturers in the pharmaceutical and life sciences sectors developing next-generation treatments.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel active pharmaceutical ingredients (APIs).
• Biochemical Research: Used as a reference standard or reagent in pharmacological and metabolic studies.
• Contract Manufacturing: Sourced by CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic Research: Employed in university and institutional labs for medicinal chemistry and drug discovery programs.
• Process Development: Utilized in the scaling and optimization of synthetic routes for pharmaceutical production.

Basic Information

Product Name	Salbupart
CAS No.	114101-13-2
Molecular Formula	C17H18F3NO3
Molecular Weight	341.33 g/mol
Synonyms	Salbupart; 2-Hydroxy-5-[1-hydroxy-2-[[2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]benzamide Trifluoroacetate; (RS)-5-[1-Hydroxy-2-({2-[4-(trifluoromethyl)phenyl]propan-2-yl}amino)ethyl]benzene-1,3-diol; Salbupart Trifluoroacetate; Salbupart TFA Salt
EINECS	Contact for details

Quality Control

Our Salbupart is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR, to ensure it meets the high standards required for pharmaceutical R&D and manufacturing. Certificates of Analysis (COA) with detailed specifications are provided for every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled accordingly to maintain stability.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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