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TCI

CAS 18822-59-8

O-tert-Butyl-L-tyrosine TCI B3212

O-tert-Butyl-L-tyrosine TCI B3212

Chemical Identity

CAS No.
18822-59-8
PubChem
CID 44629919·SID 87560422
Formula
C14H21NO3
Molecular weight
251.32 g/mol
Purity
>98.0%(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2S)-2-amino-2-methyl-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid
SMILES
C[C@](CC1=CC=C(C=C1)OC(C)(C)C)(C(=O)O)N
InChIKey
PVOLDVYXXMZPIL-AWEZNQCLSA-N
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O-tert-Butyl-L-tyrosine is a chemical compound widely used in chemical and biochemical experiments, particularly in peptide synthesis and molecular modification. As a derivative of L-tyrosine, it plays a crucial role in laboratories focused on protein research, enzyme studies, and the development of complex organic compounds. Its stable chemical structure allows for controlled modification through specific chemical reactions, making it an essential component in various synthetic processes. This compound is especially valuable for researchers aiming to create bioactive molecules or study the structural properties of proteins.

The compound is favored for its excellent chemical properties, including good solubility in organic solvents such as ethyl acetate and acetone. The presence of the tert-butyl group provides protection against unwanted chemical reactions, enhancing its stability during synthesis and application. This protective feature ensures that the compound remains chemically inert until the desired reaction conditions are met, offering greater control and precision in laboratory settings. Its reliability and predictable behavior make it a preferred choice for researchers requiring consistent results.

In Indonesian laboratories, O-tert-Butyl-L-tyrosine is extensively used in biochemical research, pharmaceutical development, and material science. Its versatility supports a wide range of experimental applications, from drug discovery to the analysis of biological compounds. The compound’s stability and reactivity make it an indispensable tool for scientists working in these fields, contributing to the advancement of scientific knowledge and innovation.

TCI brochures (PDF)

  • Peptide Synthesis: Ideal for constructing complex peptide sequences due to its stable structure and reactivity.
  • Protein Modification Studies: Used to investigate structural changes and functional properties of proteins.
  • Organic Chemistry Research: Facilitates the development of new organic compounds through controlled chemical reactions.
  • Drug Discovery: Supports the synthesis of bioactive molecules for pharmaceutical applications.
  • Biochemical Analysis: Enables the study of molecular interactions and biological activity in various systems.

Brand TCI
CAS number 18822-59-8
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light

O-tert-Butyl-L-tyrosine should be stored in a cool, dry place, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain chemical integrity. The compound is generally stable under normal laboratory conditions but should be handled with care to avoid exposure to incompatible substances. Proper labeling of storage containers is essential for safety and traceability. Laboratory personnel should wear appropriate personal protective equipment when handling this compound to ensure safe working practices. Regular inspection of storage conditions is advised to maintain the quality and usability of the material.

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