Description

(R)-Carisbamate is a high-purity, single-enantiomer compound of significant interest in advanced pharmaceutical research and development. Its primary value lies in its role as a key chiral intermediate or active pharmaceutical ingredient (API) for investigating novel therapeutic agents, particularly in the central nervous system (CNS) domain. This product is essential for pharmaceutical companies, biotechnology firms, and contract research organizations (CROs) engaged in the synthesis of enantiomerically pure drug candidates.

Application

• Pharmaceutical Intermediate: Serves as a critical chiral building block in the synthesis of novel investigational drugs.
• Neurological Research: Used in preclinical and clinical research for potential applications in epilepsy, neuropathic pain, and other CNS disorders.
• Active Pharmaceutical Ingredient (API) Development: Acts as the active moiety in the formulation development of enantiomerically pure pharmaceuticals.
• Asymmetric Synthesis: Employed as a standard or reagent in developing and validating new asymmetric catalytic processes.
• Analytical Reference Standard: Utilized as a high-purity standard for method development, validation, and quality control (HPLC, GC, chiral analysis) in analytical laboratories.
• Process Chemistry & Scale-Up: Supports chemical development teams in optimizing synthetic routes and scaling up production from milligram to kilogram quantities.

Basic Information

Product Name	(R)-Carisbamate
CAS No.	194085-74-0
Molecular Formula	C12H15NO4
Molecular Weight	237.25 g/mol
Synonyms	(R)-1,2-Ethanediol, 1-[(aminocarbonyl)oxy]-, 1-(phenylmethyl) ester; (R)-RWJ-333369; (R)-RWJ333369; (R)-YKP509; (R)-Carisbamate; (R)-Enantiomer of Carisbamate; UNII-8F5J8F7V8I; (R)-1-(Benzyloxycarbonyloxy)-2-hydroxyethane
EINECS	Contact for details

Quality Control

Our (R)-Carisbamate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical research. We provide full traceability and detailed Certificates of Analysis (COA) that include chiral purity data, assay results, and impurity profiles. Our quality commitment aligns with cGMP principles for APIs where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation. For long-term storage, consider desiccated conditions.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥98.0%
Chiral Purity (Chiral HPLC)	≥99.0% (R)-enantiomer
Related Substances (HPLC)	Total impurities ≤2.0% Any single unknown impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤0.5%

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