癸胺,1-Aminodecane
1)1-Aminodecane癸胺
英文短句/例句

1.tricaprylyl amine三辛胺和三癸胺的混合物
2.polyundecamethylene diamine sebacate聚十一烷二胺癸二酸
3.Synthesis and Physical Mechanical Properties of Poly(Decanediamine p-Phenylenedacetic Amides)聚对苯二乙酰癸二胺的制备与物理力学性能
4.Explanation the Calendar Day "癸嬛" as "癸巳" of Chu Bamboo Slips of Geling,Xincai葛陵楚简历日“癸嬛”应为“癸巳”解
5.dibutoxy ethyl sebacate癸二酸二丁氧基乙酯
6.DIDP (Di-iso-decyl Phthalate)邻苯二甲酸二异癸酯
7.hexyl octyl decyl phthalate己基辛基癸基酞酸盐
8.caprylic/capric triglyceride辛酸/癸酸三酸甘油酯
9.The isodecyl formate is considerably more stable to hydrolytic attack than the isodecyl otrhoformate.甲酸异癸酯,较原甲酸异癸酯对水解的破坏作用要安定得多。
10.Differences between Sodium Decylsulfate and Sodium Decanesulfonate when Interacting with Cationic Polyelectrolyte癸基硫酸钠和癸烷磺酸钠与阳离子聚电解质相互作用的差别
11."decane:any of various liquid isomers, CH, of the methane series.""癸烷:甲烷系的任何一种液体异构体,CH"
12.Any of various liquid isomers, C10H22, of the methane series.癸烷甲烷系的任何一种液体异构体,C10H22
13.10th heavenly stem acid cobalt, boron Xianhua cobalt adhesive production sales.癸酸钴、硼酰化钴粘合剂生产销售。
14.Study on AHL-like quorum signals in Mesorhizobium huakuii华癸根瘤菌中自体诱导物的初步研究
15.Synthesis of 1, 4-Dioxaspiro[4.5]decan-8-one;1,4-二氧杂螺[4.5]癸烷-8-酮的合成
16.Effect of Sodium Caprate on Intestinal Tract Absorption of Berberine;癸酸钠对盐酸小檗碱肠道吸收的影响
17.Catalytic Synthesis of Dibutyl Sebacate with Cupric Sulphfate;硫酸铜催化合成癸二酸二丁酯的研究
18.Scale-up Study on Lube Base Oil Prepared by Oligomerization of 1-Decene1-癸烯齐聚制备润滑油的放大研究
相关短句/例句

decanediamide癸二酰胺
1.The effects of molar ratio of raw materials, reaction time, reaction temperature and adding time of urea on decanediamide yield were examined.以癸二酸和尿素为原料合成癸二酰胺。
3)ω-decenylamineω-癸烯胺
1.Preparation of ω-decenylamine;通过Cirtis重排;首次采用化学合成方法简便地合成了ω-癸烯胺。
4)1-Aminodecane1-癸胺
5)1-Aminodecane正癸胺
6)Decamethylenediamine1,10-癸二胺
延伸阅读

癸胺分子式:C10H23N分子量:157.11CAS号:2016-57-1性质:无色透明液体,有氨臭,易燃。熔点17℃,沸点220.5℃,95.8℃(1.33kPa),相对密度0.787(20/4),折射率1.4360,闪点85℃。微溶于水,易溶于乙醇、乙醚、丙酮、苯、氯仿。制备方法:以癸酸为原料,硅胶为催化剂,在380-400℃下通氨反应得癸腈,经水洗、分层、干燥、精馏,得精癸腈。然后以镍铝为催化剂,在80℃,1.96MPa压力下加氢,至不吸氢为止,增大压力至2.35MPa,保持反应3h,放冷后放出混合物,滤去催化剂,分馏,收集199-221℃馏分,可得癸胺和副产的二癸胺,还有少量三癸胺。用途:本品为溶剂,可用于有机合成等,也可用作试剂。