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| Cangzhou Goldlion Chemicals Co., Ltd. | China | |||
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| Ring Specialty Chemicals Inc. | Canada | |||
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| Nanjing Suntton (China) Co., Ltd. | China | |||
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| Hangzhou Leap Chem Co., Ltd. | China | |||
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| Wuhan Carnoss Technology Co., Ltd. | China | |||
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| Langfang Longquan Flux Co., Ltd. | China | |||
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| Chemical manufacturer since 1988 | ||||
| Classification | Organic raw materials >> Amino compound >> Acyclic monoamines, polyamines and their derivatives and salts |
|---|---|
| Name | tert-Octylamine |
| Synonyms | 1,1,3,3-Tetramethylbutylamine; 2,4,4-Trimethyl-2-pentanamine; 2-Amino-2,4,4-trimethylpentane |
| Molecular Structure | ![]() |
| Molecular Formula | C8H19N |
| Molecular Weight | 129.24 |
| CAS Registry Number | 107-45-9 |
| EC Number | 203-491-1 |
| SMILES | CC(C)(C)CC(C)(C)N |
| Density | 0.8±0.1 g/cm3 Calc.* |
|---|---|
| Melting point | -67 °C (Expl.) |
| Boiling point | 143.4±8.0 °C 760 mmHg (Calc.)*, 137 - 143 °C (Expl.) |
| Flash point | 32.2 °C (Calc.)*, 33 °C (Expl.) |
| Solubility | water insoluble (Expl.) |
| Index of refraction | 1.431 (Calc.)*, 1.424 (Expl.) |
| Melting point | -67 °C |
| Boiling point | 137-143 °C |
| Refractive index | 1.4235-1.4255 |
| Flash point | 32 °C |
| Water solubility | insoluble |
| * | Calculated using Advanced Chemistry Development (ACD/Labs) Software. |
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| Risk Statements | H226-H290-H301-H302-H314-H318-H411 Details | ||||||||||||||||||||||||||||||||||||||||||||||||
| Safety Statements | P210-P233-P234-P240-P241-P242-P243-P260-P264-P264+P265-P270-P273-P280-P301+P316-P301+P317-P301+P330+P331-P302+P361+P354-P303+P361+P353-P304+P340-P305+P354+P338-P316-P317-P321-P330-P363-P370+P378-P390-P391-P403+P235-P405-P406-P501 Details | ||||||||||||||||||||||||||||||||||||||||||||||||
| Hazard Classification | |||||||||||||||||||||||||||||||||||||||||||||||||
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| Transport Information | UN 2734 | ||||||||||||||||||||||||||||||||||||||||||||||||
| SDS | Available | ||||||||||||||||||||||||||||||||||||||||||||||||
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tert-Octylamine is a highly branched primary amine. Its nitrogen retains ordinary amine chemistry, but the bulky carbon framework changes sterics, hydrophobicity, packing, and the physical properties of salts made from it. This makes the compound useful as a specialty intermediate rather than simply a branched substitute for straight-chain octylamine. Converting the amine into ammonium salts places an ionic head group on a bulky hydrophobic skeleton, a useful motif in surfactant-like and other functional molecules. Its story is that function belongs to more than a functional group. The amine determines what reactions are possible, while the three-dimensional carbon framework influences how easily those reactions occur and how the resulting material behaves. References: PubChem. tert-Octylamine, CAS 107-45-9. ECHA. 1,1,3,3-Tetramethylbutylamine substance information. |
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