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Sku CI23059_25_MG
Chem Impex
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Product Information

Product Name
N-Biotinyl-3,6-dioxaoctane-1,8-diamine
Brand Name
Chem Impex
Product Number
23059
CAS
138529-46-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11199678
IUPAC Name
5-(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno3,4-dimidazol-4-yl-N-2-2-(2-aminoethoxy)ethoxyethylpentanamide
InChI Key
LWISPDYGRSGXME-YDHLFZDLSA-N
SMILES
C1C@H2C@@H(C@@H(S1)CCCCC(=O)NCCOCCOCCN)NC(=O)N2

Description

N-Biotinyl-3,6-dioxaoctane-1,8-diamine is widely utilized in research focused on:

Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted therapies.

Drug Delivery Systems: Its structure enables the formulation of advanced drug delivery systems, improving the bioavailability and targeted delivery of therapeutic agents in pharmaceutical applications.

Diagnostics: The compound is used in the development of diagnostic assays, particularly in the detection of biomarkers, which can lead to early disease diagnosis and improved patient outcomes.

Research Reagents: It acts as a valuable reagent in biochemical research, facilitating various reactions and processes, such as enzyme labeling and cellular imaging, which are essential for understanding biological mechanisms.

Cosmetic Formulations: In the cosmetic industry, this compound is incorporated into formulations for its potential benefits in skin health, promoting hydration and enhancing the stability of active ingredients.

References Data Source From Pubchem

Advances in the Synthesis of Bioorthogonal Reagents: s‑Tetrazines, 1,2,4‑Triazines, Cyclooctynes, Heterocycloheptynes, and trans‑Cyclooctenes

Publication Name: Topics in Current Chemistry Collections
Publication Date: 2025
DOI: 10.1007/978-3-032-09821-4_2

Preparation and Characterization of Biocompatible Chitosan Nanoparticles for Targeted Brain Delivery of Peptides

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2018
DOI: 10.1007/978-1-4939-7571-6_36

Scutellarin inhibits Hela cell growth and glycolysis by inhibiting the activity of pyruvate kinase M2

Publication Name: Bioorganic & Medicinal Chemistry Letters
Publication Date: 2017-12-15
DOI: 10.1016/j.bmcl.2017.11.011

Advanced Immunoassays for The Direct Determination of Melatonin in Human Serum and Culture Media

Publication Name: Advances in Experimental Medicine and Biology
Publication Date: 2002
DOI: 10.1007/0-306-46814-x_56