Biotin-PEG2-amine - 98%, high purity , CAS No.138529-46-1

  • ≥98%
Item Number
B595132
Grouped product items
SKUSizeAvailabilityPrice Qty
B595132-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$117.90
B595132-250mg
250mg
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Production requires sourcing of materials. We appreciate your patience and understanding.
$236.90
B595132-500mg
500mg
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Production requires sourcing of materials. We appreciate your patience and understanding.
$454.90
B595132-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$593.90

Biotin PEG-amine

Basic Description

Synonyms(+)-Biotin-PEG2-CH2CH2NH2 | (+)-Biotin-(PEO)3-amine | Biotin-PEG2-NH2 | Biotin-PEG2-Amine | EZ-Link Amine-PEO2-Biotin | Biotin-DADOO | N-[2-[2-(2-Aminoethoxy)ethoxy]ethyl] biotinamide | biotinyl-3,6-dioxaoctanediamine | N-Biotinyl-3,6-dioxaoctane-1,8-diam
Specifications & Purity≥98%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Biotin-PEG2-amine is PEG derivative containing a biotin group and a terminal primary amine group. The amine group can be coupled to carboxyl groups or 5'phosphate groups to form stable amide bonds. The hydrophilic PEG spacer increases solubility in aqueous media of the molecules conjugated to the biotin compound. It also helps to minimize steric hindrance involved with the binding to avidin molecules.

Product description:

Biotin-DADOO is a biotinylation reagent, which can be used to synthesize a biotin-estradiol conjugate (i.e., biotin-DADOO-estradiol) to develop a direct, broad range enzyme immunoassay to measure plasma estradiol concentrations.

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-N-[2-[2-(2-aminoethoxy)ethoxy]ethyl]pentanamide
INCHI InChI=1S/C16H30N4O4S/c17-5-7-23-9-10-24-8-6-18-14(21)4-2-1-3-13-15-12(11-25-13)19-16(22)20-15/h12-13,15H,1-11,17H2,(H,18,21)(H2,19,20,22)/t12-,13-,15-/m0/s1
InChi Key LWISPDYGRSGXME-YDHLFZDLSA-N
Canonical SMILES C1C2C(C(S1)CCCCC(=O)NCCOCCOCCN)NC(=O)N2
Isomeric SMILES C1[C@H]2[C@@H]([C@@H](S1)CCCCC(=O)NCCOCCOCCN)NC(=O)N2
PubChem CID 11199678
Molecular Weight 374.49

Certificates

Certificate of Analysis(COA)

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Lot NumberCertificate TypeDateItem
A2424195Certificate of AnalysisJan 30, 2024 B595132

Chemical and Physical Properties

SolubilitySolubility in Water, DMSO, DMF
SensitivityAir & Moisture & Heat sensitive

Related Documents

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Citations of This Product

1. Dan Jia, Liyan Xiong, Xuhong Yu, Xiaofei Chen, Tingfang Wang, Alex F. Chen, Yifeng Chai, Zhenyu Zhu, Chuan Zhang.  (2019)  Cardioprotective mechanism study of salvianic acid A sodium based on a proteome microarray approach and metabolomic profiling of rat serum after myocardial infarction.  Molecular Omics,  15  (4): (271-279).  [PMID:31099812] [10.1039/C9MO00005D]

References

1. Dan Jia, Liyan Xiong, Xuhong Yu, Xiaofei Chen, Tingfang Wang, Alex F. Chen, Yifeng Chai, Zhenyu Zhu, Chuan Zhang.  (2019)  Cardioprotective mechanism study of salvianic acid A sodium based on a proteome microarray approach and metabolomic profiling of rat serum after myocardial infarction.  Molecular Omics,  15  (4): (271-279).  [PMID:31099812] [10.1039/C9MO00005D]

Solution Calculators