Fmoc-Hyp-OH TCI F0899

Chemical Identity

Other names: N-Fmoc-trans-4-hydroxy-L-proline · N-(9-Fluorenylmethyloxycarbonyl)-trans-4-hydroxy-L-proline · (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-hydroxy-L-proline
CAS No.: 88050-17-3
PubChem: CID 2756109
Formula: C20H19NO5
Molecular weight: 353.37 g/mol
Purity: >98.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,4R)-1-(9H-fluoren-9-ylmethoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid
SMILES: C1C(CN(C1C(=O)O)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)O
InChIKey: GOUUPUICWUFXPM-XIKOKIGWSA-N
MDL: MDL00151929

Rp 1.220.100,00

~~Rp 868.350,00~~ Rp 1.220.100,00

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Berat 5g 25g

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Fmoc-Hyp-OH (N-Fmoc-Hyp-OH) is a chemical compound widely used in organic reactions, particularly in peptide synthesis and aspartic acid derivatives. This compound plays a crucial role in laboratories by enabling the selective coupling of amino acids, which is fundamental to the creation of synthetic proteins and biological molecules. Its ability to participate in high-reactivity and structure-specific chemical reactions makes it an essential tool for researchers working in organic and biochemical fields. In Indonesian laboratories, Fmoc-Hyp-OH is a key reagent in various chemical processes due to its functional versatility and reliability.

One of the main reasons Fmoc-Hyp-OH is preferred is its chemical stability under specific conditions, combined with its high reactivity towards amino acid coupling agents. This dual nature allows it to be used in complex reactions without interfering with other processes, making it ideal for precision-based chemical applications. Additionally, its ability to maintain structural integrity during reactions ensures consistent results, which is vital in research settings where accuracy is paramount. The compound's compatibility with a wide range of reagents further enhances its utility in diverse chemical environments.

In Indonesian laboratories, Fmoc-Hyp-OH is commonly used in organic chemistry and biochemical research. It is a staple in projects involving the synthesis of complex molecules and the development of analytical techniques. Its widespread use in academic and research institutions highlights its importance in advancing scientific knowledge and innovation in the field of chemistry and biochemistry.

TCI brochures (PDF)

Asymmetric Organocatalysts 2025-06-12 · p. 7
Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 21

Related TCI products

Peptide Synthesis: Fmoc-Hyp-OH is ideal for peptide synthesis due to its ability to selectively couple amino acids, ensuring precise molecular structures in protein and peptide production.
Aspartic Acid Derivatives: This compound is used in the synthesis of aspartic acid derivatives, which are essential in biochemical research and pharmaceutical development.
Amino Acid Coupling Reactions: Its high reactivity with amino acid coupling agents makes it suitable for selective amino acid binding in complex chemical reactions.
Organic Chemistry Research: Fmoc-Hyp-OH is frequently used in organic chemistry experiments requiring high reactivity and structural specificity.
Biochemical Analysis: It plays a key role in biochemical analysis, supporting the development of analytical techniques for molecular structure studies.

Brand	TCI
CAS number	88050-17-3
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > Organocatalysts [Catalysis]
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light and moisture

Fmoc-Hyp-OH should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. In a laboratory setting, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Since it is a reactive chemical, it should be stored separately from incompatible substances to avoid any potential chemical interactions. Proper labeling and storage conditions ensure the safety of laboratory personnel and the integrity of the compound during its use in research applications.

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