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TCI

CAS 302-84-1

DL-Serine TCI S0034

DL-Serine TCI S0034

Chemical Identity

Other names
H-DL-Ser-OH
CAS No.
302-84-1
PubChem
CID 617·SID 87575663
Formula
C3H7NO3
Molecular weight
105.09 g/mol
Purity
>98.0%(T)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-amino-3-hydroxypropanoic acid
SMILES
C(C(C(=O)O)N)O
InChIKey
MTCFGRXMJLQNBG-UHFFFAOYSA-N
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DL-Serine is a chemical compound widely used in various scientific fields such as chemistry, biology, and pharmacy. As an essential amino acid, it plays a crucial role in protein synthesis, carbohydrate metabolism, and the formation of complex biological structures. This compound is frequently found in laboratory experiments involving peptide synthesis, molecular modification, and biochemical research. Its versatility makes it an indispensable tool for scientists working in both academic and industrial settings. DL-Serine is known for its stability and controlled reactivity, which allows it to participate in a wide range of chemical reactions and the production of complex compounds.

DL-Serine possesses several properties that make it a preferred choice in laboratory settings. It has a simple chemical structure yet is highly reactive, enabling it to interact with various molecules under both acidic and basic conditions. Its solubility in both organic solvents and water facilitates easy mixing and use in diverse experimental protocols. These characteristics contribute to its widespread application in chemical synthesis and biological research. Additionally, its chemical stability ensures consistent performance across different experimental conditions, making it a reliable reagent for scientific investigations.

In Indonesian laboratories, DL-Serine is commonly used for scientific research, educational purposes, and the development of chemical products. It supports a wide range of experimental activities, from basic research to advanced biochemical studies. Its availability and reliability make it a valuable resource for both academic institutions and research organizations in Indonesia. The compound’s ability to participate in multiple reactions enhances its utility in various laboratory applications, contributing to the advancement of scientific knowledge and innovation.

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  • Peptide Synthesis: DL-Serine is essential in the synthesis of peptides due to its amino acid structure, enabling the formation of complex protein-like molecules.
  • Molecular Modification: Its reactivity allows for the modification of molecular structures, supporting research in organic chemistry and biochemistry.
  • Biochemical Research: DL-Serine is frequently used in biochemical experiments to study metabolic pathways and enzyme activity.
  • Educational Purposes: It serves as a key teaching material in chemistry and biology courses, helping students understand amino acid functions and reactions.
  • Pharmaceutical Development: DL-Serine is used in the development of pharmaceutical compounds due to its role in biological processes and its chemical versatility.

Brand TCI
CAS number 302-84-1
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in various quantities as per supplier specifications
Physical form White crystalline powder
Storage Store in a cool, dry place away from moisture and direct sunlight

DL-Serine should be stored in a cool, dry place away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical stability, it does not require refrigeration, but it should be kept in a secure location to avoid accidental spills or contamination. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling the compound. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in experiments. Always follow standard laboratory safety protocols to ensure safe handling and storage.

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