N-Biotinyl-3,6-dioxaoctane-1,8-diamine trifluoroacetate salt solution

• Catalog No.: 11184
• CAS Number: 194920-57-5
• M. F.: C18H31F3N4O6S
• M. W.: 488.5221496
• Purity: ≥95% (TLC)

SYNONYMS

• Title: N-Biotinyl-3,6-dioxaoctane-1,8-diamine
• IUPAC name: 5-[(3aS,4S,6aR)-2-oxo-hexahydro-1H-thieno[3,4-d]imidazolidin-4-yl]-N-{2-[2-(2-aminoethoxy)ethoxy]ethyl}pentanamide; trifluoroacetic acid
• IUPAC Traditional name: 5-[(3aS,4S,6aR)-2-oxo-hexahydrothieno[3,4-d]imidazolidin-4-yl]-N-{2-[2-(2-aminoethoxy)ethoxy]ethyl}pentanamide; trifluoroacetic acid
• Synonyms: Biotin-DADOO; N-{2-[2-(2-Aminoethoxy)ethoxy]ethyl}biotinamide trifluoroacetate salt; N-{2-[2-(2-Aminoethoxy)ethoxy]ethyl}biotinamide

DATABASE IDS

• CAS Number: 194920-57-5
• MDL Number: MFCD11114063

PROPERTIES

• Concentration: 25 mg/mL in DMSO
• Empirical Formula (Hill Notation): C16H30N4O4S · C2HF3O2
• Purity: ≥95% (TLC)
• Solubility: DMF: soluble
• Personal Protective Equipment: Eyeshields, Gloves
• Storage Temperature: 2-8°C
• German water hazard class: 2

DETAILS

Description (English)

Packaging
Sold on the basis of grams of solution.Product 11184-1G contains 1 gram of solution (approximately 910 microliters), at a concentration of 25 mg/mL (~23 mg N-Biotinyl-3,6-dioxaoctane-1,8-diamine trifluoroacetate salt).
Application
Utilized to biotinylate thiomethyl and thiosulfate derivatives of carboxymethylcellulose through a DCC coupling reaction Labeling targets include glycoproteins, glycopeptides, and any aldehyde- or keto group-containing component (e.g., haptens) Utilized to synthesize a biotin-estradiol conjugate (i.e., biotinoyl-diaminodioxaoctane-estradiol derivative) to develop a direct, broad range enzyme immunoassay to measure plasma estradiol concentrations.

Description (简体中文)

包装
Sold on the basis of grams of solution.Product 11184-1G contains 1 gram of solution (approximately 910 microliters), at a concentration of 25 mg/mL (~23 mg N-Biotinyl-3,6-dioxaoctane-1,8-diamine trifluoroacetate salt).
Application
Utilized to biotinylate thiomethyl and thiosulfate derivatives of carboxymethylcellulose through a DCC coupling reaction Labeling targets include glycoproteins, glycopeptides, and any aldehyde- or keto group-containing component (e.g., haptens) Utilized to synthesize a biotin-estradiol conjugate (i.e., biotinoyl-diaminodioxaoctane-estradiol derivative) to develop a direct, broad range enzyme immunoassay to measure plasma estradiol concentrations.