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3-Buten-1-amine, tech. 90%, Thermo Scientific Chemicals
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Catalog number L20157.06
also known as L20157-06
Price (USD)/ Each
496.65
Online exclusive
584.00 Save 87.35 (15%)
-
Quantity:
5 g
Price (USD)/ Each
496.65
Online exclusive
584.00 Save 87.35 (15%)
3-Buten-1-amine, tech. 90%, Thermo Scientific Chemicals
Catalog numberL20157.06
Price (USD)/ Each
496.65
Online exclusive
584.00 Save 87.35 (15%)
-
Chemical Identifiers
CAS2524-49-4
Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to yellow
Assay (GC)≥88.0%
FormLiquid
Refractive Index1.4210-1.4270 @ 20?C
3-Buten-1-amine is an aliphatic terminal amine used for organic synthesis and in proteomics research. Its hydrochloride salt is used to improve the detection of neurodegenerative alzheimer’s disease in ELISA titrations by reducing the background due to non-specific associations of molecules and proteins.
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
3-Buten-1-amine is an aliphatic terminal amine used for organic synthesis and in proteomics research. Its hydrochloride salt is used to improve the detection of neurodegenerative alzheimer’s disease in ELISA titrations by reducing the background due to non-specific associations of molecules and proteins.
Solubility
Miscible with water.
Notes
Incompatible with strong acids, strong oxidizing agents and strong bases.
3-Buten-1-amine is an aliphatic terminal amine used for organic synthesis and in proteomics research. Its hydrochloride salt is used to improve the detection of neurodegenerative alzheimer’s disease in ELISA titrations by reducing the background due to non-specific associations of molecules and proteins.
Solubility
Miscible with water.
Notes
Incompatible with strong acids, strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Colin, O.; Greck, C.; Prim, D.; Thomassigny, C. Toward Pyridine-Heterocycle Patterns through Prins and Aza-Prins Cyclisations: Application to a Short Synthesis of (±)-Anabasine. Eur. J. Org. Chem. 2014, 2014 (31), 7000-7005.
- Saika, F.; Kiguchi, N.; Kobayashi, Y.; Kishioka, S. Peripheral alpha4beta2 nicotinic acetylcholine receptor signalling attenuates tactile allodynia and thermal hyperalgesia after nerve injury in mice. Acta Physiologica 2015, 213 (2), 462-471.