Being Search helps find more words for games such as Combination,Permutation,Scrabble and Word With Friends, triethylamine.See more.

Sorry no words found in database but here are some following intersting information is available for triethylamine

No direct (one word) anagrams for triethylamine found in this word list.

The word triethylamine uses 13 total characters with white space

The word triethylamine uses 13 total characters with white out space

The word "triethylamine" uses 10 unique characters: A E H I L M N R T Y

Number of all permutations npr for triethylamine 3628800

Number of all combination ncr for triethylamine 3628800

2 same character containing word for triethylamine

All permutations word for triethylamine

All combinations word for triethylamine

All similar letter combinations related to triethylamine

From Wikipedia

Triethylamine
Skeletal formula of triethylamine
Ball and stick model of triethylamine
Spacefill model of triethylamine
Names
Preferred IUPAC name
N,N-Diethylethanamine
Other names
(Triethyl)amine
Triethylamine (deprecated[1])
Identifiers
CAS Number
  • 121-44-8 YesY
3D model (JSmol)
  • Interactive image
AbbreviationsTEA[2]
Beilstein Reference
605283
ChEBI
  • CHEBI:35026 YesY
ChemSpider
  • 8158 YesY
ECHA InfoCard100.004.064
EC Number204-469-4
KEGG
  • C14691 YesY
MeSHtriethylamine
PubChem CID
  • 8471
RTECS numberYE0175000
UNII
  • VOU728O6AY YesY
UN number1296
Properties[4]
Chemical formula
C6H15N
Molar mass101.19 g·mol−1
AppearanceColourless liquid
OdorFishy, ammoniacal
Density0.7255 g mL−1
Melting point−114.70 °C; −174.46 °F; 158.45 K
Boiling point88.6 to 89.8 °C; 191.4 to 193.5 °F; 361.7 to 362.9 K
log P1.647
Vapor pressure6.899–8.506 kPa
66 μmol Pa−1 kg−1
Acidity (pKa)10.75 (for the conjugate acid) (H2O), 9.00 (DMSO) [3]
Magnetic susceptibility (χ)
-81.4·10−6 cm3/mol
Refractive index (nD)
1.401
Thermochemistry
216.43 J K−1 mol−1
−169 kJ mol−1
−4.37763 to −4.37655 MJ mol−1
Hazards
GHS pictogramsThe flame pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The corrosion pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The exclamation-mark pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal wordDANGER
GHS hazard statements
H225, H302, H312, H314, H332
GHS precautionary statements
P210, P280, P305+351+338, P310
NFPA 704
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g., gasolineHealth code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gasReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
3
3
0
Flash point−15 °C (5 °F; 258 K)
312 °C (594 °F; 585 K)
Explosive limits1.2–8%
Threshold limit value
2 ppm (8 mg/m3) (TWA), 
4 ppm (17 mg/m3) (STEL)
Lethal dose or concentration (LD, LC):
LD50 (median dose)
  • 580 mg kg−1 (dermal, rabbit)
  • 730 mg kg−1 (oral, rat)
LCLo (lowest published)
1425 ppm (mouse, 2 hr)[6]
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 25 ppm (100 mg/m3)[5]
REL (Recommended)
None established[5]
IDLH (Immediate danger)
200 ppm[5]
Related compounds
Related amines
  • Dimethylamine
  • Trimethylamine
  • N-Nitrosodimethylamine
  • Diethylamine
  • Diisopropylamine
  • Dimethylaminopropylamine
  • Diethylenetriamine
  • N,N-Diisopropylethylamine
  • Triisopropylamine
  • Tris(2-aminoethyl)amine
  • Mechlorethamine
  • HN1 (nitrogen mustard)
  • HN3 (nitrogen mustard)
Related compounds
  • Unsymmetrical dimethylhydrazine
  • Biguanide
  • Dithiobiuret
  • Agmatine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Triethylamine is the chemical compound with the formula N(CH2CH3)3, commonly abbreviated Et3N. It is also abbreviated TEA, yet this abbreviation must be used carefully to avoid confusion with triethanolamine or tetraethylammonium, for which TEA is also a common abbreviation. It is a colourless volatile liquid with a strong fishy odor reminiscent of ammonia and is also the smell of the hawthorn plant.[7] Like diisopropylethylamine (Hünig’s base), triethylamine is commonly encountered in organic synthesis.

  1. ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 671. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. 
  2. ^ X. Bories-Azeau, S. P. Armes, and H. J. W. van den Haak, Macromolecules 2004, 37, 2348 PDF
  3. ^ Cite error: The named reference David Evans Research Group was invoked but never defined (see the help page).
  4. ^ The Merck Index (11th ed.). 9582. 
  5. ^ a b c "NIOSH Pocket Guide to Chemical Hazards #0633". National Institute for Occupational Safety and Health (NIOSH). 
  6. ^ "Triethylamine". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH). 
  7. ^ The Hawthorn, BBC

From Wiktionary

English[edit]

Noun[edit]

Wikipedia has an article on:
triethylamine
Wikipedia

triethylamine (countable and uncountable, plural triethylamines)

  1. (organic chemistry) The tertiary amine (CH3-CH2)3N, having many industrial uses.