(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine TCI A1301

Chemical Identity

CAS No.: 22795-99-9
PubChem: CID 643457·SID 87562761
Formula: C7H16N2
Molecular weight: 128.22 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(2S)-1-ethylpyrrolidin-2-yl]methanamine
SMILES: CCN1CCC[C@H]1CN
InChIKey: UNRBEYYLYRXYCG-ZETCQYMHSA-N

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(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine is a chiral building block widely used in asymmetric synthesis to create molecules with optical activity. This compound is essential in the field of organic chemistry, where precise control over stereochemistry is crucial. Its unique structure, featuring a modified pyrrolidine ring with an amino and ethyl group, allows it to serve as a versatile intermediate in the synthesis of complex organic compounds. In laboratory settings, it is frequently employed as a starting material for the development of pharmaceuticals and specialty chemicals. Its role in creating enantiomerically pure products makes it a valuable tool for researchers aiming to achieve high specificity in their chemical reactions.

The compound's chemical stability and reactivity make it a preferred choice for various synthetic applications. Its chiral nature ensures that it can participate in asymmetric reactions to yield products with defined stereochemistry, which is essential in drug development and fine chemical manufacturing. The compound’s ability to selectively interact with other chiral reagents or catalysts enhances its utility in controlled synthesis processes. This makes it particularly suitable for applications where precise molecular structure is required, such as in the development of bioactive compounds and advanced materials.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, pharmaceutical development, and studies on chiral reactivity. It is a key component in the work of academic institutions and research centers focused on asymmetric synthesis and molecular structure analysis. Its widespread use in both academic and industrial settings highlights its importance in advancing chemical research and innovation in Indonesia.

TCI brochures (PDF)

Asymmetric Organocatalysts 2025-06-12 · p. 7
Asymmetric Synthesis 2026-03-18 · p. 8
Chiral Building Blocks 2025-04-14 · p. 3

Related TCI products

Pharmaceutical synthesis for the development of enantiomerically pure drugs requiring precise stereochemical control.
Organic chemistry research focused on asymmetric catalysis and chiral molecule construction.
Industrial chemical production involving the creation of complex organic compounds with specific optical properties.
Academic studies on the reactivity and stereochemical behavior of chiral building blocks.
Drug discovery programs aiming to optimize the pharmacological activity of new compounds through controlled synthesis.

Brand	TCI
CAS number	22795-99-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid or crystalline, depending on formulation
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and maintain chemical integrity. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended racemization or degradation. In a laboratory setting, it should be kept in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn during handling. Proper labeling of containers is essential to ensure safe storage and usage.

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