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1,4-Diaminobutane, 98+%, Thermo Scientific Chemicals
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Catalog number B21316.22
also known as B21316-22
Price (USD)/ Each
69.65
Online exclusive
77.20 Save 7.55 (10%)
-
Quantity:
100 g
Price (USD)/ Each
69.65
Online exclusive
77.20 Save 7.55 (10%)
1,4-Diaminobutane, 98+%, Thermo Scientific Chemicals
Catalog numberB21316.22
Price (USD)/ Each
69.65
Online exclusive
77.20 Save 7.55 (10%)
-
Chemical Identifiers
CAS110-60-1
IUPAC Namebutane-1,4-diamine
Molecular FormulaC4H12N2
InChI KeyKIDHWZJUCRJVML-UHFFFAOYSA-N
SMILESNCCCCN
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Specifications
Specification Sheet
Specification SheetRefractive Index1.4540-1.4590 @ 20?C
Appearance (Color)Clear colorless to pale yellow
FormLiquid as melt
Identification (FTIR)Conforms
Assay (GC)≥98.0%
1,4-Diaminobutane is used as a precursor in many biological systems and synthon for amido-ureas. It is involved in the synthesis of nylon 46 by reacting with adipic acid.
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
1,4-Diaminobutane is used as a precursor in many biological systems and synthon for amido-ureas. It is involved in the synthesis of nylon 46 by reacting with adipic acid.
Solubility
Soluble in ether and alcohol.
Notes
Incompatible with acids, strong oxidizing agents, aldehydes, acid anhydrides and acid chlorides.
1,4-Diaminobutane is used as a precursor in many biological systems and synthon for amido-ureas. It is involved in the synthesis of nylon 46 by reacting with adipic acid.
Solubility
Soluble in ether and alcohol.
Notes
Incompatible with acids, strong oxidizing agents, aldehydes, acid anhydrides and acid chlorides.
RUO – Research Use Only
General References:
- Ahmed, N. C-B.; Negadi, L.; Mokbel, I.; Jose, J. Phase equilibrium properties of binary aqueous solutions containing ethanediamine, 1,2-diaminopropane, 1,3-diaminopropane, or 1,4-diaminobutane at several temperatures. J. Chem. Thermodyn. 2011,43 (5), 719-724.
- Kim, Y. E.; Yun, S. H.; Choi, J. H.; Nam, S. C.; Park, S. Y.; Jeong, S. K.; Yoon, Y. Comparison of the CO2 Absorption Characteristics of Aqueous Solutions of Diamines: Absorption Capacity, Specific Heat Capacity, and Heat of Absorption. Energy Fuels. 2015, 29 (4), 2582-2590.
- Hoang, G. T.; Kubo, T.; Young, V. G.; Kautzky, J. A.; Wissinger, J. E. Illustrating the Utility of X-ray Crystallography for Structure Elucidation through a Tandem Aldol Condensation/Diels-Alder Reaction Sequence. J. Chem. Educ. 2015, 92 (8), 1381-1384.