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ChemicalBook--->CAS DataBase List--->663171-32-2

663171-32-2

663171-32-2 Structure

663171-32-2 Structure
IdentificationBack Directory
[Name]

1H-Thieno[3,4-d]imidazole-4-pentanamide,N-(14-amino-3,6,9,12-tetraoxatetradec-1-yl)hexahydro-2-oxo-,(3aS,4S,6aR)-
[CAS]

663171-32-2
[Synonyms]

Biotin-PEG4-NH2
(+)-BIOTIN-PEG4-AMINE
(+)-Biotin-PEG4-CH2CH2NH2
(+)-Biotin-PEG4-CH2CH2NH2
(+)-Biotin-PEG4-amine
N-Biotinyl-3,6,9,12-tetraoxatetradecane-1,14-diamine
N-[2-[2-[2-[2-(2-Aminoethoxy)ethoxy]ethoxy]ethoxy]ethyl]biotinamide
N-(17-amino-3,6,9,12,15-pentaoxaheptadecyl)-5-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
(3aS,4S,6aR)-N-(14-Amino-3,6,9,12-tetraoxatetradec-1-yl)hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanamide
1H-Thieno[3,4-d]imidazole-4-pentanamide,N-(14-amino-3,6,9,12-tetraoxatetradec-1-yl)hexahydro-2-oxo-,(3aS,4S,6aR)-
N-(14-Amino-3,6,9,12-tetraoxatetradecyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
N-(14-Amino-3,6,9,12-tetraoxatetradec-1-yl)-5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanamide
5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-N-[2-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]ethyl]pentanamide
[Molecular Formula]

C20H38N4O6S
[MDL Number]

MFCD26142992
[MOL File]

663171-32-2.mol
[Molecular Weight]

462.604
Chemical PropertiesBack Directory
[Boiling point ]

724.4±60.0 °C(Predicted)
[density ]

1.161±0.06 g/cm3(Predicted)
[solubility ]

Soluble in Water, DCM, Ethanol
[form ]

powder to lump
[pka]

13.90±0.40(Predicted)
[color ]

White to Almost white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2934999090
Hazard InformationBack Directory
[Description]

Biotin-PEG4-amine is a popular biotinylation reagent with PEG spacer. It can be coupled to carboxyl groups or 5'phosphate groups to form stable amide bonds. PEG spacer increases aqueous solubility of the molecules conjugated to the biotin compound. It also helps to minimize steric hindrance involved with the binding to avidin molecules.
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