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R(+)-Uh-301 Hcl CAS NO 127126-18-5


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CAS No.:127126-18-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

R(+)-Uh-301 Hcl is a high-purity chiral compound identified by CAS NO 127126-18-5, serving as a critical intermediate in advanced pharmaceutical synthesis and research. This enantiomerically pure substance is essential for developing and scaling up active pharmaceutical ingredients (APIs) with specific stereochemical requirements. It is primarily utilized by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic research institutions focused on medicinal chemistry and process development.

Application

  • Pharmaceutical Intermediate: Key building block in the synthesis of novel therapeutic agents, particularly where the R(+) enantiomer is pharmacologically active.
  • Chiral Catalyst Research: Used in the development and study of asymmetric synthesis methodologies and chiral resolution processes.
  • Reference Standard: Serves as a high-purity analytical standard for method development and quality control in regulatory submissions.
  • Medicinal Chemistry: Employed in structure-activity relationship (SAR) studies and lead optimization for new drug candidates.
  • Process Chemistry: Integral to pilot-scale and commercial-scale manufacturing processes for enantiomerically pure drugs.
  • Academic & Institutional Research: Used in university and institutional labs for advanced organic synthesis and pharmacological research projects.

Basic Information

Product Name R(+)-Uh-301 Hcl
CAS No. 127126-18-5
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms (R)-UH-301 hydrochloride; (+)-UH-301 HCl; 127126-18-5; UH-301, (R)-, hydrochloride; R enantiomer of UH-301 hydrochloride; (R)-UH301 hydrochloride salt; UH-301 R(+) form HCl salt
EINECS Contact for details

Quality Control

Our R(+)-Uh-301 Hcl is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including chiral purity assay and identification of key impurities, to meet the stringent requirements of pharmaceutical development. Certificates of Analysis (COA) detailing purity, enantiomeric excess, and other critical parameters are provided with every shipment and are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 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. For long-term storage, consider using desiccants.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Purity (HPLC) ≥ 98.0%
Enantiomeric Excess (Chiral HPLC) ≥ 99.0%
Loss on Drying ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm

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

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