Detail of > 121-44-8
- MSDS Download

- CAS Number:
- 121-44-8
- Name:
Triethylamine
- Formula:
- C6H15N
- Molecular Structure:

- Synonyms:
- Triethylamine(7CI,8CI);(Diethylamino)ethane;N,N-Diethylethanamine;AI3-15425;CCRIS 4881;Ethanamine, N,N-diethyl-;HSDB 896;Triaethylamin;Trietilamina;
- Molecular Weight:
- 101.19
- EINECS:
- 204-469-4
- Density:
- 0.75 g/cm3
- Melting Point:
- -115 °C
- Boiling Point:
- 90.495 °C at 760 mmHg
- Solubility:
- water: 133 g/L (20 °C)
- Appearance:
- colorless liquid
- Hazard Symbols:
F,
C- Risk Codes:
- 11-20/21/22-35
- Safety:
- 3-16-26-29-36/37/39-45Details
- Transport Information:
- UN 1296 3/PG 2
- Deleted CAS:
- 144514-14-7|168277-99-4|172227-74-6|449752-61-8|750564-56-8
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Reference
- Electrolyte circulation type metal-halogen secondary battery
- Electrolyte circulation type metal-halogen secondary battery. Fujii, Toshinobu; Kokado, Akira (Meidensha K. K., Japan). Eur. Pat. Appl. EP 91520 A1 19 Oct 1983, 19 pp. DESIGNATED STATES: R: DE, FR, GB, IT. (English). (European Patent Organization). CODEN: EPXXDW. CLASS: IC: H01M010-36; H01M002-40; H01M004-38. APPLICATION: EP 82-301919 14 Apr 1982. DOCUMENT TYPE: Patent CA Section: 52 (Electrochemical, Radiational, and Thermal Energy Technology) In the title battery a cell chamber is divided into a cathode and an anode chamber by a separator, and the cathode chamber and anode chamber are resp. connected to a catholyte-storage tank and an anolyte-storage tank. It is possible to avoid Br, discharged at the anode, passing into the cathode chamber from the anolyte by including in the anolyte a tertiary alkylamine as complexing agent. The resulting complex is oily and can be pumped with the anolyte into the anolyte storage tank, where it can ppt.In this experiment, several chemicals are used like 121-44-8 and 75-50-3 Advantageously, the anolyte also contains an acid, most preferably in an amt. equimolar with the amine. .
- Comparative consideration on the catalytic activity of 1,4-diazabicyclo[2
- Comparative consideration on the catalytic activity of 1,4-diazabicyclo[2.2.2]octane in the formation of urethane and urea. Thiele, Lothar (Zentralinst. Org. Chem., Dtsch. Akad. Wiss., Berlin-Adlershof, Ger. Dem. Rep.). Plaste Kautsch., 30(12), 668-70 (German) 1983. 280-57-9 and 121-44-8 are also in the experiment. CODEN: PLKAAM. ISSN: 0048-4350. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) Section cross-reference(s): 67 The superior catalytic activity of 1,4-diazabicyclo[2.2.2]octane over Et3N in the title processes is explained on stereochem. grounds. .
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