إثيلامين ثلاثي

إثيلامين ثلاثي
الأسماء
	اسم أيوپاك المفضل N,N-Diethylethanamine
	أسماء أخرى (Triethyl)amine; Triethylamine (no longer IUPAC name)
Identifiers
رقم CAS
3D model (JSmol)	Interactive image;
اختصارات	TEA
مرجع بايلستاين	605283
ChEBI	CHEBI:35026 ;
ChEMBL	ChEMBL284057 ;
ChemSpider	8158 ;
ECHA InfoCard	100.004.064
رقم EC	204-469-4;
KEGG	C14691 ;
عناوين مواضيع طبية MeSH	{{{value}}}
PubChem CID	8471;
رقم RTECS	YE0175000;
UNII	VOU728O6AY ;
UN number	1296
CompTox Dashboard (EPA)	DTXSID3024366 ;
InChI	InChI={{{value}}}
SMILES
الخصائص
الصيغة الجزيئية	C6H15N
كتلة مولية	101.19 g mol-1
المظهر	Colourless liquid
الرائحة	Fishy, ammoniacal
الكثافة	0.7255 g mL−1
نقطة الانصهار
نقطة الغليان
log P	1.647
ضغط البخار	6.899–8.506 kPa
kH	66 μmol Pa−1 kg−1
الحموضة (pKa)	10.75 (for the conjugate acid) (H2O), 9.00 (DMSO)
القابلية المغناطيسية	-81.4·10−6 cm3/mol
معامل الانكسار (nD)	1.401
الكيمياء الحرارية
الإنتالپية المعيارية; للتشكل ΔfHo298	−169 kJ mol−1
الانتالبية المعيارية; للاحتراق ΔcHo298	−4.37763 to −4.37655 MJ mol−1
سعة الحرارة النوعية، C	216.43 J K−1 mol−1
المخاطر
ن.م.ع. مخطط تصويري
ن.م.ع. كلمة الاشارة	DANGER
ن.م.ع. عبارات المخاطر	H225, H302, H312, H314, H332
ن.م.ع. العبارات الاحتياطية	P210, P280, P305+P351+P338, P310
NFPA 704 (معيـَّن النار)	3 3 0
نقطة الوميض	−15 °C (5 °F; 258 K)
درجة حرارة; الاشتعال الذاتي	312 °C (594 °F; 585 K)
حدود الانفجار	1.2–8%
قيمة حد العتبة	2 ppm (8 mg/m3) (TWA), ; 4 ppm (17 mg/m3) (STEL)
	الجرعة أو التركيز القاتل (LD, LC):
LD50 (الجرعة الوسطى)	580 mg kg−1 (dermal, rabbit); 730 mg kg−1 (oral, rat);
LCLo (المنشورة الأقل)	1425 ppm (mouse, 2 hr)
	حدود التعرض الصحية بالولايات المتحدة (NIOSH):
PEL (المسموح)	TWA 25 ppm (100 mg/m3)
REL (الموصى به)	None established
IDLH (خطر عاجل)	200 ppm
مركبات ذا علاقة
amines ذات العلاقة	Dimethylamine; Trimethylamine; N-Nitrosodimethylamine; Diethylamine; Diisopropylamine; Dimethylaminopropylamine; Diethylenetriamine; N,N-Diisopropylethylamine; Triisopropylamine; Tris(2-aminoethyl)amine; Mechlorethamine; HN1 (nitrogen mustard); HN3 (nitrogen mustard);
مركـّبات ذات علاقة	Unsymmetrical dimethylhydrazine; Biguanide; Dithiobiuret; Agmatine;
	ما لم يُذكر غير ذلك، البيانات المعطاة للمواد في حالاتهم العيارية (عند 25 °س [77 °ف]، 100 kPa).
	verify (what is ?)
	مراجع الجدول

إثيلامين ثلاثي أو تراي‌إثيلامين Triethylamine هو مركب كيميائي صيغته 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.^[6]^[7] It is a colourless volatile liquid with a strong fishy odor reminiscent of ammonia. Like diisopropylethylamine (Hünig's base), triethylamine is commonly employed, usually as a base, in organic synthesis.

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

التخليق والخصائص

Triethylamine is prepared by the alkylation of ammonia with ethanol:^[8]

NH₃ + 3 C₂H₅OH → N(C₂H₅)₃ + 3 H₂O

The pK_a of protonated triethylamine is 10.75,^[3] and it can be used to prepare buffer solutions at that pH. The hydrochloride salt, triethylamine hydrochloride (triethylammonium chloride), is a colorless, odorless, and hygroscopic powder, which decomposes when heated to 261 °C.

Triethylamine is soluble in water to the extent of 112.4 g/L at 20 °C.^[9] It is also miscible in common organic solvents, such as acetone, ethanol, and diethyl ether.

Laboratory samples of triethylamine can be purified by distilling from calcium hydride.^[10]

In alkane solvents triethylamine is a Lewis base that forms adducts with a variety of Lewis acid such as I₂ and phenols. Owing to its steric bulk, it forms complexes with transition metals reluctantly.

التطبيقات

Triethylamine is commonly employed in organic synthesis as a base. For example, it is commonly used as a base during the preparation of esters and amides from acyl chlorides.^[11] Such reactions lead to the production of hydrogen chloride which combines with triethylamine to form the salt triethylamine hydrochloride, commonly called triethylammonium chloride. This reaction removes the hydrogen chloride from the reaction mixture, which can be required for these reactions to proceed to completion (R, R' = alkyl, aryl):

R₂NH + R'C(O)Cl + Et₃N → R'C(O)NR₂ + Et₃NH⁺Cl⁻

Like other tertiary amines, it catalyzes the formation of urethane foams and epoxy resins. It is also useful in dehydrohalogenation reactions and Swern oxidations.

Triethylamine is readily alkylated to give the corresponding quaternary ammonium salt:

RI + Et₃N → Et₃NR⁺I⁻

Triethylamine is mainly used in the production of quaternary ammonium compounds for textile auxiliaries and quaternary ammonium salts of dyes. It is also a catalyst and acid neutralizer for condensation reactions and is useful as an intermediate for manufacturing medicines, pesticides and other chemicals.

Triethylamine salts like any other tertiary ammonium salts are used as an ion-interaction reagent in ion interaction chromatography, due to their amphiphilic properties. Unlike quaternary ammonium salts, tertiary ammonium salts are much more volatile, therefore mass spectrometry can be used while performing analysis.

استخدامات صغيرة

Triethylamine is used to give salts of various carboxylic acid-containing pesticides, e.g. Triclopyr and 2,4-dichlorophenoxyacetic acid^{[بحاجة لمصدر]}

Triethylamine is the active ingredient in FlyNap, a product for anesthetizing Drosophila melanogaster.^{[بحاجة لمصدر]} Triethylamine is used in mosquito and vector control labs to anesthetize mosquitoes. This is done to preserve any viral material that might be present during species identification.

Also, the bicarbonate salt of triethylamine (often abbreviated TEAB, triethylammonium bicarbonate) is useful in reverse phase chromatography, often in a gradient to purify nucleotides and other biomolecules.^{[بحاجة لمصدر]}

Triethylamine was found during the early 1940s to be hypergolic in combination with nitric acid, and was considered a possible propellant for early hypergolic rocket engines.^[12]

التواجد الطبيعي

Hawthorn flowers have a heavy, complicated scent, the distinctive part of which is triethylamine, which is also one of the first chemicals produced by a dead human body when it begins to decay. For this reason, it is considered unlucky to bring hawthorn into a house. Gangrene and semen are also said to possess a similar odour.^[13]

المراجع

^ "Front Matter". 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.
^ X. Bories-Azeau, S. P. Armes, and H. J. W. van den Haak, Macromolecules 2004, 37, 2348 PDF
^ ^أ ^ب David Evans Research Group Archived 2012-01-21 at the Wayback Machine
^ ^أ ^ب ^ت NIOSH Pocket Guide to Chemical Hazards 0633
^ "Triethylamine". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
^ "Ethanolamine Compounds (MEA, DEA, TEA And Others)". Safe Cosmetics (in الإنجليزية الأمريكية). Retrieved 2020-06-17.
^ "tetraethylammonium | Ligand page | IUPHAR/BPS Guide to PHARMACOLOGY". www.guidetopharmacology.org. Retrieved 2020-06-17.
^ Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2000). Amines, Aliphatic. doi:10.1002/14356007.a02_001. ISBN 3527306730.
^ "MSDS - 471283". www.sigmaaldrich.com. Retrieved 2020-06-17.
^ F., Armarego, W. L. (2012-10-17). Purification of Laboratory Chemicals. Chai, Christina Li Lin (Seventh ed.). Amsterdam. ISBN 9780123821621. OCLC 820853648.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: multiple names: authors list (link)
^ Sorgi, K. L. (2001). "Triethylamine". Encyclopedia of Reagents for Organic Synthesis. New York: John Wiley & Sons. doi:10.1002/047084289X.rt217. ISBN 978-0471936237.
^ Clark, John (1972). Ignition!: An Informal History of Liquid Rocket Propellants (PDF). Rutgers University, the State University of New Jersey. p. 13. ISBN 0-8135-0725-1.
^ The book of general ignorance. John Lloyd & John Mitchinson. Faber & Faber 2006, The Hawthorn, BBC

وصلات خارجية

[1] "Front Matter". 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

[David_Evans_Research_Group-3] أ ^ب David Evans Research Group Archived 2012-01-21 at the Wayback Machine

[PGCH-4] أ ^ب ^ت NIOSH Pocket Guide to Chemical Hazards 0633

[5] "Triethylamine". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

[6] "Ethanolamine Compounds (MEA, DEA, TEA And Others)". Safe Cosmetics (in الإنجليزية الأمريكية). Retrieved 2020-06-17.

[7] "tetraethylammonium | Ligand page | IUPHAR/BPS Guide to PHARMACOLOGY". www.guidetopharmacology.org. Retrieved 2020-06-17.

[Ullmann-8] Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2000). Amines, Aliphatic. doi:10.1002/14356007.a02_001. ISBN 3527306730.

[9] "MSDS - 471283". www.sigmaaldrich.com. Retrieved 2020-06-17.

[10] F., Armarego, W. L. (2012-10-17). Purification of Laboratory Chemicals. Chai, Christina Li Lin (Seventh ed.). Amsterdam. ISBN 9780123821621. OCLC 820853648.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: multiple names: authors list (link)

[11] Sorgi, K. L. (2001). "Triethylamine". Encyclopedia of Reagents for Organic Synthesis. New York: John Wiley & Sons. doi:10.1002/047084289X.rt217. ISBN 978-0471936237.

[Clark-12] Clark, John (1972). Ignition!: An Informal History of Liquid Rocket Propellants (PDF). Rutgers University, the State University of New Jersey. p. 13. ISBN 0-8135-0725-1.

[13] The book of general ignorance. John Lloyd & John Mitchinson. Faber & Faber 2006, The Hawthorn, BBC

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وبينار	مصادر	صور	الأخبار	فيديو