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(Boc-aminooxy)acetic acid, 98+%, Thermo Scientific Chemicals
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Catalog number H54109.06
also known as H54109-06
Price (USD)/ Each
273.00
-
Quantity:
5 g
Price (USD)/ Each
273.00
(Boc-aminooxy)acetic acid, 98+%, Thermo Scientific Chemicals
Catalog numberH54109.06
Price (USD)/ Each
273.00
-
Chemical Identifiers
CAS42989-85-5
IUPAC Name2-({[(tert-butoxy)carbonyl]amino}oxy)acetic acid
Molecular FormulaC7H13NO5
InChI KeyQBXODCKYUZNZCY-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)NOCC(O)=O
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)>98.0%
(Boc-aminooxy)acetic acid was employed to introduce a hydroxylamine moiety into peptides; reaction with an aldehyde to an oxime. It was used in the preparation of Boc-aminooxy tetra(ethylene glycol).
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(Boc-aminooxy)acetic acid was employed to introduce a hydroxylamine moiety into peptides; reaction with an aldehyde to an oxime. It was used in the preparation of Boc-aminooxy tetra(ethylene glycol).
Solubility
Soluble in methanol.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
(Boc-aminooxy)acetic acid was employed to introduce a hydroxylamine moiety into peptides; reaction with an aldehyde to an oxime. It was used in the preparation of Boc-aminooxy tetra(ethylene glycol).
Solubility
Soluble in methanol.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Karen L.Christman; Rebecca M.Broyer; Zachary P.Tolstyka; Heather D.Maynard. Site-specific protein immobilization through N-terminal oxime linkages. J. Mater. Chem. 2007, 17, (19),2021-2027
- Damien Forget; Dr. Didier Boturyn; Dr. Eric Defrancq; Prof. Jean Lhomme; Prof. Pascal Dumy. Highly efficient synthesis of peptide-oligonucleotide conjugates: Chemoselective oxime and thiazolidine formation. Chemistry - A European Journal. 2001, 7, (18),3976-3984