Biotin-X
| Code | Size | Price |
|---|
| CDX-B0143-M100 | 100 mg | £108.00 |
Quantity:
| CDX-B0143-M500 | 500 mg | £401.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Antibody Isotype: n/a
Antibody Clone: n/a
Regulatory Status: RUO
Shipping:
Ambient
Storage:
-20°C
Documents
Further Information
Alternate Names/Synonyms:
N-(+)-Biotinyl-6-aminohexanoic acid; Biotin caproic acid; (+)-Biotin-epsilon-aminocaproic acid; 6-((Biotinoyl)amino)hexanoic acid; N-(+)-Biotinyl-6-aminocaproic acid
Appearance:
White to off-white powder.
CAS:
72040-64-3
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Protect from light and moisture.
InChi:
InChI=1S/C16H27N3O4S/c20-13(17-9-5-1-2-8-14(21)22)7-4-3-6-12-15-11(10-24-12)18-16(23)19-15/h11-12,15H,1-10H2,(H,17,20)(H,21,22)(H2,18,19,23)/t11-,12-,15-/m0/s1
InChiKey:
CMUGHZFPFWNUQT-HUBLWGQQSA-N
Long Description:
Chemical. CAS: 72040-64-3. Formula: C16H27N3O4S. MW: 357.47. Biotin-X is an amino-reactive biotinylation reagent with a long spacer arm. The 6-aminocaproic acid spacer arm provides distance between the biotin and the target ligand which helps alleviate steric hindrance. Biotin-X can be used to biotinylate antibodies, proteins, peptides, or amino acids by reacting with primary amines as found in the N-terminus and Lysine side chains. Biotin-X may also be used in the biosynthesis of biotinylated oligosaccharides. Optimal reaction conditions are at a pH of 7-9. Avoid amine-containing buffers, which may compete in the acylation reaction.
MDL:
MFCD00144853
Molecular Formula:
C16H27N3O4S
Molecular Weight:
357.47
Package Type:
Vial
Product Description:
Biotin-X is an amino-reactive biotinylation reagent with a long spacer arm. The 6-aminocaproic acid spacer arm provides distance between the biotin and the target ligand which helps alleviate steric hindrance. Biotin-X can be used to biotinylate antibodies, proteins, peptides, or amino acids by reacting with primary amines as found in the N-terminus and Lysine side chains. Biotin-X may also be used in the biosynthesis of biotinylated oligosaccharides. Optimal reaction conditions are at a pH of 7-9. Avoid amine-containing buffers, which may compete in the acylation reaction.
Purity:
>98% (HPLC)
SMILES:
O=C(NCCCCCC(O)=O)CCCC[C@@H]1SC[C@@]2([H])[C@]1([H])NC(N2)=O
Solubility Chemicals:
Soluble in DMSO or DMF (slightly).
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) G.T. Hermanson; Bioconjugate Techn. 2nd p506-545 (2008)