QBD10728
m-dPEG®36-OH
>90% (HPLC)
Synonym(s):
m-PEG36-OH, mPEG-alcohol, mPEG1500, mPEG36-OH, mPEG36-alcohol
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About This Item
Empirical Formula (Hill Notation):
C73H148O37
Molecular Weight:
1617.93
UNSPSC Code:
12352200
NACRES:
NA.22
MDL number:
Assay:
>90% (HPLC)
Form:
solid or viscous liquid
SMILES string
O(CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOC)CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO
InChI key
BYLIGSNYHOODII-UHFFFAOYSA-N
assay
>90% (HPLC)
form
solid or viscous liquid
reaction suitability
reaction type: Pegylations
polymer architecture
shape: linear
functionality: monofunctional
shipped in
ambient
storage temp.
−20°C
Features and Benefits
m-dPEG36-OH is a chemical modification reagent. It consists of a methyl-terminated, water-soluble, non-immunogenic, single molecular weight, discrete polyethylene glycol (dPEG) chain. The dPEG chain is 109 atoms (130.1 Å) long and terminates with a reactive hydroxy group. The hydroxy group can be functionalized with different groups that enable various types of reactions. Uses for this monodisperse equivalent of an m-PEG1500-OH include surface passivation and biomolecule modification.
Legal Information
Products Protected under U.S. Patent #s 7,888,536 & 8,637,711 and European Patent #s 1,594,440 & 2,750,681
dPEG is a registered trademark of Quanta BioDesign
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Hadi M Zareie et al.
ACS nano, 2(4), 757-765 (2009-02-12)
Self-assembled monolayers (SAMs) of oligo(ethylene glycol) (OEG)-tethered molecules on gold are important for various biorelevant applications ranging from biomaterials to bioanalytical devices, where surface resistance to nonspecific protein adsorption is needed. Incorporation of a stimuli-responsive character to the OEG SAMs
Jin Sha et al.
Biomacromolecules, 14(9), 3294-3303 (2013-08-14)
Multicomponent poly(ethylene glycol) (PEG) brushes (i.e., ≥ 2 adjacent PEG brushes) can be used to engineer culture substrates with microscale, nonfouling regions decorated with covalently immobilized ligands that mediate biospecific interactions. However, synthesizing such brushes with orthogonal immobilization chemistries to
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