Fmoc-6-Ahx-OH TCI F1319

Chemical Identity

Other names: Fmoc-6-aminohexanoic Acid · 6-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]hexanoic Acid · Fmoc-epsilon-aminocaproic Acid · Fmoc-ε-Aca-OH
CAS No.: 88574-06-5
Formula: C21H23NO4
Molecular weight: 353.42 g/mol
Purity: >95.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 6-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCCCCC(=O)O
InChIKey: FPCPONSZWYDXRD-UHFFFAOYSA-N
MDL: MDL00077045
PubChem: CID 2756087

Rp 795.900,00

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Berat 5g 25g

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Fmoc-6-Ahx-OH (N-Fmoc-6-aminohexanoic acid) is a chemical compound widely used in peptide synthesis and the creation of bioactive molecules. As a building block in chemical reactions, it plays a crucial role in constructing complex molecular structures. This compound is commonly found in chemical and biochemical laboratories, serving as a key reagent for the synthesis of biologically active compounds. Its stability and reactivity make it a reliable choice for researchers aiming to develop new therapeutic agents and molecular tools.

The compound’s functional group, Fmoc (9-fluorenylmethyloxycarbonyl), enables specific and efficient deprotection reactions, which are essential in peptide synthesis. This feature allows for precise control over amino acid coupling, making it highly desirable in the field of organic chemistry. The Fmoc group also ensures compatibility with various synthetic methodologies, enhancing the versatility of this compound in laboratory settings.

In Indonesian laboratories, Fmoc-6-Ahx-OH is frequently utilized in pharmacology, biochemistry, and organic chemistry research. Scientists from educational and research institutions rely on this compound to develop new compounds with potential medical applications. Its role in drug discovery and molecular design underscores its importance in advancing scientific innovation within the region.

Peptide Synthesis: Fmoc-6-Ahx-OH is ideal for synthesizing peptides due to its Fmoc group, which allows for controlled and efficient coupling reactions.
Bioactive Compound Development: The compound is used in the creation of bioactive molecules, supporting research into new therapeutic agents.
Organic Chemistry Research: Its stability and reactivity make it a preferred choice for complex molecular synthesis in organic chemistry laboratories.
Pharmaceutical Research: The compound plays a key role in drug discovery, enabling the development of new pharmaceutical compounds.
Biomedical Applications: It is widely used in biochemical studies to explore molecular interactions and biological functions.

Brand	TCI
CAS number	88574-06-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from light

Fmoc-6-Ahx-OH should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. The compound is generally stable under standard laboratory conditions, but care should be taken to avoid prolonged exposure to heat or reactive substances. Proper labeling and safe handling procedures are essential to ensure the integrity of the compound and the safety of laboratory personnel. Always follow standard chemical handling protocols to minimize risks associated with chemical exposure.

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