氨三乙腈

氨三乙腈
	IUPAC名; 2,2′,2′′-Nitrilotriacetonitrile
別名	三(氰甲基)胺; 2,2',2''-氮川三乙腈
識別
CAS編號	7327-60-8
PubChem	81762
ChemSpider	73778
SMILES	C(C#N)N(CC#N)CC#N;
InChI	1S/C6H6N4/c7-1-4-10(5-2-8)6-3-9/h4-6H2;
InChIKey	LJAIDEYQVIJERM-UHFFFAOYSA-N
性質
化學式	C6H6N4
摩爾質量	134.14 g·mol−1
熔點	125 °C（398 K）
結構
空間群	Pnma
晶格常數	a = 7.1085, b = 9.9320, c = 9.3869
危險性
	GHS危險性符號;
GHS提示詞	危險
H-術語	H301, H302, H312, H315, H319, H335, H373
P-術語	P260, P261, P264, P270, P271, P280, P301+310, P301+312, P302+352, P304+340, P305+351+338, P312, P314, P321
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

氨三乙腈（NTAN）是一種有機化合物，化學式為C₆H₆N₄，它是氨三乙酸、三(胺乙基)胺（英語：Tris(2-aminoethyl)amine）和胺乙基哌嗪的前驅體。

合成

氨三乙腈可由甲醛、氨和氰化氫在酸性水溶液中通過氨的氰甲基化反應得到。^[2]^[3]

氨氣進入反應體系，以六亞甲基四胺^[4]或硫酸銨的形式和甲醛水溶液（通常為37wt%）在pH<2的調節下與氰化氫在100 °C反應得到。^[5]在生產過程中，尤其是連續反應的情況下，低於90 °C時，氨三乙腈會沉澱出來，堵塞反應器管路，導致熱失控。 ^[6]

應用

在鹼性催化劑（如甲醇鈉）存在下，氨三乙腈可與亞胺基二乙腈在熔體中均聚或共聚，形成深色的固體聚合物，它在1000°C以上可碳化形成含氮導電聚合物。^[7]

氨三乙腈在氫化時，其中一個氰基會轉化為亞胺基，相比於亞胺基的進一步氫化，它傾向於進攻另一個相鄰的氰基以形成穩定的六元環。催化氫化的最終產物是胺乙基哌嗪。

在雷尼鎳等催化劑存在下、氨過量時進行氫化，氨三乙腈會轉化為三(胺乙基)胺（英語：Tris(2-aminoethyl)amine）^[8]。

三(胺乙基)胺（tren）的合成。

得到的這種化合物（簡寫tren）可用作四齒配體和過渡金屬離子形成穩定的螯合物。^[9]

氨三乙腈和甲醛在pH 9.5下反應，得到2,2-二羥甲基氨三乙腈，它在氫氧化鈉溶液中於100 °C水解，得到2,2-二羥甲基氨三乙酸三鈉，酸化後得到2,2-二羥甲基氨三乙酸。^[10]

該化合物可作為重金屬離子或鹼土金屬離子的絡合劑，如作為漂白劑（過硼酸鈉等）的穩定劑和作為洗滌助洗劑，用於抑制紡織品在洗滌過程中產生水垢。

氨三乙腈在硫酸中水解，可以定量產生氨三乙酰胺，它可用作金屬配位的中性四齒配體。^[11]升高溫度，通過閉環反應可以得到3,5-二氧代哌嗪-1-乙酰胺，中和後在過量氨水中加熱，也可以定量轉化為氨三乙酰胺。^[12]^[13]

氨三乙腈在酸性或鹼性條件下水解，可以得到氨三乙酸及其鈉鹽。^[14]^[2]反應中可能產生的CN⁻可以通過氧化後處理（如在pH 8下使用次氯酸鈉氧化）去除。^[15]

Alkaline hydrolysis of NTAN to NTA trisodium salt

它和鹽酸羥胺、氫氧化鈉在乙醇水溶液中反應，可以得到四齒配體氮三乙酰胺肟，它可以螯合Cu²⁺。^[16]

參考文獻

^ Dubsky, J. V.; Wensink, W. D. Direct nitration of aliphatic imino compounds. II. Action of absolute nitric acid on 3,5-diketo-1-acetamidohexahydro-1,4-diazine. Berichte der Deutschen Chemischen Gesellschaft. 1916, 49: 1041–1044. ISSN 0365-9496. CODEN BDCGAS
^ ^2.0 ^2.1 US 3337607,J.C. Wollensak,「Process for preparation of an amine nitrile」,發表於1967-08-22
^ US 3840581,H. Neumaier, W. Vogt, K. Sennewald, R. Schuller, G. Lenz,「Process for the manufacture of nitrilotriacetonitrile」,發表於1974-10-08
^ US 3061628,J.J. Singer Jr., M. Weisberg,「Process and preparation of amino nitriles and acetic acids」,發表於1962-10-30
^ EP 0102343,C.Y. Shen,「Process for producing nitrilotriacetonitrile」,發表於1986-02-26
^ E. Fiedler, Emergency Runaway Reaction – What Precedes? What Follows?, Chem. Engineer. Transactions (CET) 48, 2016, 48: 361–366, ISBN 978-88-95608-39-6, doi:10.3303/CET1648061
^ US 3578643,L.L. Wood, R.A. Hamilton,「New polymers from nitrilotriacetonitrile and iminodiacetonitrile」,發表於1971-05-11
^ US 3565957,S.B. Mirviss, D.J. Martin, E.D. Weil,「Hydrogenation of nitrilotriacetonitrile」,發表於1971-02-23
^ G. Anderegg; V. Gramlich, 1:1 Metal Complexes of Bivalent Cobalt, Nickel, Copper, Zink, and Cadmium with the Tripodal Ligand tris[2-(dimethylamino)ethyl]amine: Their stabilities and the X-ray crystal structure of its copper(II) complex sulfate, Helv. Chim. Acta 77 (3), 1994, 77 (3): 685–690, doi:10.1002/hlca.19940770312
^ EP 0396999,A. Oftring, S. Birnbach, R. Bauer, C. Gousetis, W. Trieselt,「2-Methyl- und 2-Hydroxymethyl-serin-N,N-diessigsäure und ihre Derivate」,發表於1990-11-14
^ D.A. Smith; S. Sucheck; S. Cramer; D. Baker, Nitrilotriacetamide: Synthesis in concentrated sulfuric acid and stability in water, Synth. Commun. 25 (24), 1995, 25 (24): 4123–4132, doi:10.1080/00397919508011491
^ GB 1170399,「A process for preparing 3,5-dioxo-1-piperazineacetamide and nitrilotriacetic acid triamide」,發表於1969-11-12
^ D.A. Smith; S. Cramer; S. Sucheck; E. Skrzypzak-Jankun, Facile synthesis of substituted nitrilotriacetamides, Tetrahedron Lett. 33 (50), 1992, 33 (50): 7765–7768, doi:10.1016/0040-4039(93)88040-P
^ US 4547589,C.Y. Shen,「Hydrolysis of nitrilotriacetonitrile」,發表於1985-10-15
^ US 8362298,O.M. Falana, A. Hikem, S.R. Kakadjian, F. Zamora,「Hydrolyzed nitrilotriacetonitrile compositions, nitrilotriacetonitrile hydrolysis formulations and methods for making and using same」,發表於2013-01-29
^ Pearse, George A.; Raithby, Paul R.; Maughan, Maria M.J. Synthesis and x-ray crystal structure of 2,2′,2″-iminotris(acetamidoxime) copper(II) sulphate monohydrate, [CuN(CH₂CNH₂:NOH)₃(SO₄)]·H₂O. Polyhedron. 1994-01, 13 (4): 553–558 [2022-08-02]. ISSN 0277-5387. doi:10.1016/S0277-5387(00)84731-2. （原始內容存檔於2018-06-26）.

[1] Dubsky, J. V.; Wensink, W. D. Direct nitration of aliphatic imino compounds. II. Action of absolute nitric acid on 3,5-diketo-1-acetamidohexahydro-1,4-diazine. Berichte der Deutschen Chemischen Gesellschaft. 1916, 49: 1041–1044. ISSN 0365-9496. CODEN BDCGAS

[Ethyl-2] 2.0 ^2.1 US 3337607,J.C. Wollensak,「Process for preparation of an amine nitrile」,發表於1967-08-22

[Knapsack-3] US 3840581,H. Neumaier, W. Vogt, K. Sennewald, R. Schuller, G. Lenz,「Process for the manufacture of nitrilotriacetonitrile」,發表於1974-10-08

[4] US 3061628,J.J. Singer Jr., M. Weisberg,「Process and preparation of amino nitriles and acetic acids」,發表於1962-10-30

[5] EP 0102343,C.Y. Shen,「Process for producing nitrilotriacetonitrile」,發表於1986-02-26

[6] E. Fiedler, Emergency Runaway Reaction – What Precedes? What Follows?, Chem. Engineer. Transactions (CET) 48, 2016, 48: 361–366, ISBN 978-88-95608-39-6, doi:10.3303/CET1648061

[7] US 3578643,L.L. Wood, R.A. Hamilton,「New polymers from nitrilotriacetonitrile and iminodiacetonitrile」,發表於1971-05-11

[8] US 3565957,S.B. Mirviss, D.J. Martin, E.D. Weil,「Hydrogenation of nitrilotriacetonitrile」,發表於1971-02-23

[9] G. Anderegg; V. Gramlich, 1:1 Metal Complexes of Bivalent Cobalt, Nickel, Copper, Zink, and Cadmium with the Tripodal Ligand tris[2-(dimethylamino)ethyl]amine: Their stabilities and the X-ray crystal structure of its copper(II) complex sulfate, Helv. Chim. Acta 77 (3), 1994, 77 (3): 685–690, doi:10.1002/hlca.19940770312

[10] EP 0396999,A. Oftring, S. Birnbach, R. Bauer, C. Gousetis, W. Trieselt,「2-Methyl- und 2-Hydroxymethyl-serin-N,N-diessigsäure und ihre Derivate」,發表於1990-11-14

[11] D.A. Smith; S. Sucheck; S. Cramer; D. Baker, Nitrilotriacetamide: Synthesis in concentrated sulfuric acid and stability in water, Synth. Commun. 25 (24), 1995, 25 (24): 4123–4132, doi:10.1080/00397919508011491

[12] GB 1170399,「A process for preparing 3,5-dioxo-1-piperazineacetamide and nitrilotriacetic acid triamide」,發表於1969-11-12

[13] D.A. Smith; S. Cramer; S. Sucheck; E. Skrzypzak-Jankun, Facile synthesis of substituted nitrilotriacetamides, Tetrahedron Lett. 33 (50), 1992, 33 (50): 7765–7768, doi:10.1016/0040-4039(93)88040-P

[14] US 4547589,C.Y. Shen,「Hydrolysis of nitrilotriacetonitrile」,發表於1985-10-15

[Falana-15] US 8362298,O.M. Falana, A. Hikem, S.R. Kakadjian, F. Zamora,「Hydrolyzed nitrilotriacetonitrile compositions, nitrilotriacetonitrile hydrolysis formulations and methods for making and using same」,發表於2013-01-29

[16] Pearse, George A.; Raithby, Paul R.; Maughan, Maria M.J. Synthesis and x-ray crystal structure of 2,2′,2″-iminotris(acetamidoxime) copper(II) sulphate monohydrate, [CuN(CH₂CNH₂:NOH)₃(SO₄)]·H₂O. Polyhedron. 1994-01, 13 (4): 553–558 [2022-08-02]. ISSN 0277-5387. doi:10.1016/S0277-5387(00)84731-2. （原始內容存檔於2018-06-26）.

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