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Thermo Scientific Chemicals
2-Ethylhexylamine, 98%
CAS: 104-75-6 | C8H19N | 129.247 g/mol
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Catalog number A10372.0F
also known as A10372-0F
Price (USD)
163.65
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Online exclusive
Ends: 30-Jun-2026
192.00Save 28.35 (15%)
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Quantity:
2500 mL
Price (USD)
163.65
Special offer
Online exclusive
Ends: 30-Jun-2026
192.00Save 28.35 (15%)
Each
Chemical Identifiers
CAS104-75-6
IUPAC Name3-(aminomethyl)heptane
Molecular FormulaC8H19N
InChI KeyLTHNHFOGQMKPOV-UHFFFAOYNA-N
SMILESCCCCC(CC)CN
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
FormLiquid
Assay (GC)≥97.5%
Refractive Index1.4290-1.4330 @ 20?C
2-Ethylhexylamine is used to make pharmaceuticals and other chemicals. It is used as beam material and surface active agent. It also involves in synthesis of aliphatic amines.
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
2-Ethylhexylamine is used to make pharmaceuticals and other chemicals. It is used as beam material and surface active agent. It also involves in synthesis of aliphatic amines.
Solubility
Soluble in water. 2.5 g/L (20°C)
Notes
Air Sensitive. Incompatible with strong oxidizing agents. Protect against electrostatic charges. Store away from acid chlorides and acid anhydrides.
2-Ethylhexylamine is used to make pharmaceuticals and other chemicals. It is used as beam material and surface active agent. It also involves in synthesis of aliphatic amines.
Solubility
Soluble in water. 2.5 g/L (20°C)
Notes
Air Sensitive. Incompatible with strong oxidizing agents. Protect against electrostatic charges. Store away from acid chlorides and acid anhydrides.
RUO – Research Use Only
M Miura; M Toriyama; S Motohashi. Novel Synthesis of Optically Active 2-Ethylhexanoic Acid, 2-Ethylhexanol, and 2-Ethylhexylamine via the Asymmetric Favorskii Rearrangement.Synthetic communications. 2006, 36 259-264.