Description

Cyclohexanamine, 5-Methyl-2-(1-Methylethyl)-, (2R,5S)-Rel- (9Ci) CAS NO 787534-09-2 is a high-purity, stereochemically defined chiral amine building block. This compound is valued for its role as a critical intermediate in the synthesis of complex, biologically active molecules, offering precise control over the final product's stereochemistry. It is primarily sought after by research institutions and manufacturers in the pharmaceutical and agrochemical industries for developing novel active ingredients and fine chemicals.

Application

• Pharmaceutical Intermediate: A key chiral synthon in the research and development of new active pharmaceutical ingredients (APIs), particularly for central nervous system (CNS) and anti-infective drugs.
• Agrochemical Synthesis: Used in the production of advanced pesticides and herbicides where specific stereochemistry is required for optimal efficacy and environmental profile.
• Catalyst Ligand Precursor: Serves as a starting material for synthesizing chiral ligands used in asymmetric catalysis, enabling more efficient and selective chemical transformations.
• Fine Chemical Production: Employed in the manufacture of specialty chemicals, flavors, and fragrances that require high-purity, enantiomerically enriched intermediates.
• Academic & Industrial Research: A valuable reagent for methodological studies in organic synthesis and medicinal chemistry for exploring new synthetic routes.

Basic Information

Product Name	Cyclohexanamine, 5-Methyl-2-(1-Methylethyl)-, (2R,5S)-Rel- (9Ci)
CAS No.	787534-09-2
Molecular Formula	C10H21N
Molecular Weight	155.28 g/mol
Synonyms	(1R,2S,5R)-2-Isopropyl-5-methylcyclohexanamine; rel-(1R,2S,5R)-2-Isopropyl-5-methylcyclohexanamine; (2R,5S)-rel-5-Methyl-2-(propan-2-yl)cyclohexan-1-amine; Chiral Menthylamine Isomer; Stereoisomer of Menthylamine; (1R,2S,5R)-Menthylamine (rel); Contact for additional synonyms.
EINECS	Contact for details

Quality Control

Our production of this chiral amine adheres to strict quality management systems. Each batch is characterized using advanced analytical techniques including chiral HPLC, GC, and NMR to ensure high enantiomeric excess (ee) and chemical purity. A comprehensive Certificate of Analysis (COA) detailing identity, purity, assay, and impurity profiles is provided with every shipment to guarantee batch-to-batch consistency and traceability for your critical R&D and cGMP manufacturing processes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed under an inert atmosphere (e.g., nitrogen or argon) after opening to prevent degradation.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Assay (GC/HPLC)	≥ 98.0%
Enantiomeric Excess (Chiral HPLC)	≥ 99.0%
Water Content (KF)	≤ 0.5%

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