Description

(S,S)-(-)-N,N'-Bis(α-Methylbenzyl)Sulfamide CAS NO 27304-75-2 is a high-purity chiral sulfamide derivative, valued for its role as a versatile chiral auxiliary and resolving agent in asymmetric synthesis. Its significance lies in enabling the production of enantiomerically pure compounds, which is critical for pharmaceutical efficacy and regulatory approval. This product is essential for research and development chemists, process development scientists, and manufacturers in the pharmaceutical, agrochemical, and fine chemical industries who require high stereochemical control.

Application

• Chiral Auxiliary in Asymmetric Synthesis: Used to induce chirality in the synthesis of complex organic molecules, including active pharmaceutical ingredients (APIs).
• Resolution of Racemic Mixtures: Employed as a resolving agent to separate enantiomers of acids, amines, and other chiral compounds.
• Pharmaceutical Intermediate: Serves as a key building block in the development of novel therapeutic agents, particularly in central nervous system (CNS) and cardiovascular drug candidates.
• Catalyst and Ligand Precursor: Acts as a precursor for the synthesis of chiral ligands used in metal-catalyzed asymmetric reactions.
• Agrochemical Research: Utilized in the development of enantiomerically pure pesticides and herbicides to improve activity and reduce environmental impact.
• Academic and R&D Laboratories: A valuable tool for methodological studies in organic chemistry and stereochemistry.

Basic Information

Product Name	(S,S)-(-)-N,N'-Bis(α-Methylbenzyl)Sulfamide
CAS No.	27304-75-2
Molecular Formula	C16H20N2O2S
Molecular Weight	304.41 g/mol
Synonyms	(S,S)-N,N'-Bis(1-Phenylethyl)sulfamide; (S,S)-(-)-N,N'-Bis(α-Methylbenzyl)sulfamide; (1S,1'S)-N,N'-Bis(1-Phenylethyl)sulfamide; Sulfamide, N,N'-bis[(1S)-1-phenylethyl]-; (S,S)-Bis(α-methylbenzyl)sulfamide; (S,S)-Bis(1-phenylethyl)sulfamide; (S,S)-DABS; (S,S)-BMS
EINECS	Contact for details

Quality Control

Our (S,S)-(-)-N,N'-Bis(α-Methylbenzyl)Sulfamide is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including chiral purity verification by HPLC, to ensure compliance with exacting research and process development standards. Comprehensive Certificates of Analysis (COA) detailing identity, purity, and enantiomeric excess are provided to guarantee batch-to-batch consistency and traceability.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from heat, sparks, and open flame. The product is light-sensitive (store away from light).

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Enantiomeric Excess (Chiral HPLC)	≥ 99.0%
Melting Point	Contact for details
Loss on Drying	≤ 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.