N-Boc-1,4-diaminobutane, 97+%, Thermo Scientific Chemicals
N-Boc-1,4-diaminobutane, 97+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

N-Boc-1,4-diaminobutane, 97+%, Thermo Scientific Chemicals

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Quantity:
5 mL
1 mL
Catalog number H56499.AA
also known as H56499-AA
Price (USD)/ Each
346.00
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Quantity:
5 mL
Request bulk or custom format
Price (USD)/ Each
346.00
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N-Boc-1,4-diaminobutane, 97+%, Thermo Scientific Chemicals
Catalog numberH56499.AA
Price (USD)/ Each
346.00
-
Add to cart
Chemical Identifiers
CAS68076-36-8
IUPAC Nametert-butyl N-(4-azaniumylbutyl)carbamate
Molecular FormulaC9H21N2O2
InChI KeyZFQWJXFJJZUVPI-UHFFFAOYSA-O
SMILESCC(C)(C)OC(=O)NCCCC[NH3+]
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Colorless to yellow
Assay (GC)98%
FormLiquid
N-Boc-1,4-diaminobutane is used in preparation of pharmacologically active compounds, preparation of spermidine analogues and in introduction of a C4-spacer. It serve as intermediates of medicine.

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
N-Boc-1,4-diaminobutane is used in preparation of pharmacologically active compounds, preparation of spermidine analogues and in introduction of a C4-spacer. It serve as intermediates of medicine.

Notes
Incompatible with oxidizing agents. Store at room temperature.
RUO – Research Use Only

General References:

  1. R. Jin.; L.S. Moreira Teixeira.; P.J. Dijkstra.; C.A. van Blitterswijk.; M. Karperien.; J. Feijena. Enzymatically-crosslinked injectable hydrogels based on biomimetic dextran-hyaluronic acid conjugates for cartilage tissue engineering.Biomaterials. 2010, 31 (11), 3103-3113.
  2. Jerry Ryan Holder.; Rayna M Bauzo.; Zhimin Xiang, Joseph Scott.; Carrie Haskell-Luevano. Design and pharmacology of peptoids and peptide-peptoid hybrids based on the melanocortin agonists core tetrapeptide sequence. Bioorg. Med. Chem. Lett. 2003, 13 (24),4505-4509.