N-Succinimidyl Tetradecanoate TCI S0997

Chemical Identity

CAS No.: 69888-86-4
PubChem: CID 4229289·SID 354334635
Formula: C18H31NO4
Molecular weight: 325.4 g/mol
Purity: >95.0%(HPLC)(N)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2,5-dioxopyrrolidin-1-yl) tetradecanoate
SMILES: CCCCCCCCCCCCCC(=O)ON1C(=O)CCC1=O
InChIKey: NZEDHZOVUDEBGW-UHFFFAOYSA-N

Rp 4.425.750,00

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N-Succinimidyl Tetradecanoate is a chemical compound widely used in bioconjugation applications within laboratory settings. It serves as an activation reagent that facilitates the covalent bonding of biological molecules such as proteins, peptides, and nucleic acids to various substrates. This compound plays a crucial role in enabling the formation of stable and specific molecular linkages, which are essential in many biochemical and biotechnological processes. Its utility spans across multiple research areas, making it a versatile tool for scientists working in chemical biology and related fields.

The compound's effectiveness is largely due to its highly specific chemical properties. It is capable of reacting with amino groups on target molecules, allowing for precise and controlled conjugation reactions. This specificity ensures that the resulting conjugates maintain their structural and functional integrity, which is vital for applications requiring high accuracy. Additionally, its chemical stability under standard laboratory conditions contributes to its reliability and ease of use, making it a preferred choice for researchers.

In Indonesian laboratories, N-Succinimidyl Tetradecanoate is commonly used in biomedical research, organic chemistry, and biotechnology. It is a key component in various experimental protocols, including protein immobilization and the synthesis of bioconjugates. Its high quality and consistent performance make it a trusted reagent among research institutions and academic laboratories in Indonesia.

TCI brochures (PDF)

Human-Serum-Albumin Binding Agents for Improvement of Pharmacokinetics 2019-02-22 · p. 1

Related TCI products

Bioconjugation Research - This item is ideal for creating stable covalent bonds between biomolecules, enabling precise molecular modifications in biochemical experiments.
Protein Immobilization - Its ability to react with amino groups makes it suitable for attaching proteins to solid surfaces, which is essential in biosensor development.
Peptide Conjugation - The compound facilitates the attachment of peptides to various substrates, supporting applications in drug development and molecular biology.
Nucleic Acid Modification - It enables the conjugation of nucleic acids to other molecules, which is useful in genetic engineering and molecular diagnostics.
Surface Functionalization - Its reactivity with amino groups allows for the modification of surfaces in lab-based applications such as microarray fabrication.

From the TCI brochure

Myristoylation reagent; fatty acid derivative shown among those reported to bind albumin

Brand	TCI
CAS number	69888-86-4
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Bioconjugation
Pack sizes	Available in various quantities as per standard laboratory reagent packaging
Physical form	Solid or liquid depending on the specific formulation
Storage	Store in a cool, dry place away from direct light and moisture

N-Succinimidyl Tetradecanoate should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and humidity, which could affect its reactivity. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe usage. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Proper labeling of storage containers is essential for safe handling and to prevent accidental exposure. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.

References cited in the TCI brochure

P Kurtzhals. Albumin binding of insulins acylated with fatty acids: characterization of the ligand-protein interaction and correlation between binding affinity and timing of the insulin effect in vivo Biochemical Journal, 1995. doi:10.1042/bj3120725
Batya Plotkin. Insulin Mimetic Action of Synthetic Phosphorylated Peptide Inhibitors of Glycogen Synthase Kinase-3 The Journal of Pharmacology and Experimental Therapeutics, 2003. doi:10.1124/jpet.102.047381
Ib Jonassen. Design of the Novel Protraction Mechanism of Insulin Degludec, an Ultra-long-Acting Basal Insulin Pharmaceutical Research, 2012. doi:10.1007/s11095-012-0739-z
Yuanyan Tan. Myristic acid-modified thymopentin for enhanced plasma stability and immune-modulating activity International Immunopharmacology, 2017. doi:10.1016/j.intimp.2017.03.025