N-(tert-Butoxycarbonyl)-L-tyrosine TCI B1640

Chemical Identity

Other names: Boc-Tyr-OH
CAS No.: 3978-80-1
PubChem: CID 117439·SID 87564541
Formula: C14H19NO5
Molecular weight: 281.30 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChEBI

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O
InChIKey: CNBUSIJNWNXLQQ-NSHDSACASA-N

Rp 955.500,00

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N-(tert-Butoxycarbonyl)-L-tyrosine is a chemical compound widely used in chemical and biochemical experiments. It is a protected amino acid derivative, where the hydroxyl group of tyrosine is masked by the tert-butoxycarbonyl (Boc) group. This protection allows for controlled chemical reactions and selective modifications during synthesis. In laboratory settings, this compound plays a crucial role in peptide chemistry, particularly in the synthesis of peptides and organic compounds. Its stability and controlled reactivity make it a reliable choice for researchers working in various fields.

The compound’s unique properties, including its stability and controlled reactivity, make it a preferred choice for synthetic chemists. The Boc group provides a protective shield that prevents unwanted side reactions, ensuring the integrity of the target molecule during synthesis. This makes it ideal for applications requiring high specificity and precision. Its chemical specificity allows for efficient deprotection under controlled conditions, which is vital in the development of pharmaceuticals and bioactive compounds.

In Indonesian laboratories, N-(tert-Butoxycarbonyl)-L-tyrosine is commonly used in biochemical and pharmaceutical research. It supports the development of new drugs and the study of biological processes. Its versatility and reliability make it a key reagent in both academic and industrial research settings. Researchers in Indonesia rely on this compound for its consistent performance and wide range of applications.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 12

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its protective Boc group, which allows for controlled deprotection and selective modification during the synthesis process.
Organic Chemistry Research: It is used in organic chemistry for the synthesis of complex molecules where controlled reactivity and stability are essential.
Biochemical Analysis: Its role in protecting functional groups makes it valuable in biochemical studies involving amino acid derivatives and protein modifications.
Pharmaceutical Development: The compound is widely used in the development of new drugs, where precise chemical modifications are required for drug efficacy and stability.
Environmental Studies: It is employed in environmental research to study the behavior of organic compounds in different chemical environments.

Brand	TCI
CAS number	3978-80-1
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid powder
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its stability. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is not flammable but may react with strong acids or bases. Ensure proper ventilation in the laboratory when handling this compound. Always follow standard laboratory safety protocols to minimize any potential risks associated with its use.

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