2,3,5-Trimethylpyrazine

October 2021 Trimethylpyrazine.svg 150px 2,3,5-Trimethylpyrazine Pyrazine, 2,3,5-trimethyl-;2,3,5-Trimethyl pyrazine;2,3,5-Trimethyl pyrazine (natural);2,3,5-Trimethylpyrazine;2,3,6-Trimethylpyrazine;5-23-05-00419 (Beilstein Handbook Reference);AI3-34442;BRN 0002423;CCRIS 2932;FEMA No. 3244;Pyrazine, trimethyl-;Trimethylpyrazine 14667-55-1 correct CAS 26808 320146 24972 190131 238-712-0 Q8PR0W8TIT correct FDA 1S/C7H10N2/c1-5-4-8-6(2)7(3)9-5/h4H,1-3H3 IAEGWXHKWJGQAZ-UHFFFAOYSA-N CC1=CN=C(C(=N1)C)C 7 10 2 colourless to slightly yellow liquid roasted nut, baked potato odour 0.979 g mL−1 173.1 Alcohol, oils, water (1.521e+004 mg/L at 25 °C (est) 1.5030 to 1.5050 02 07 Warning 226 302 210 233 240 241 242 243 264 270 280 301+312 303+361+353 330 370+378 403+235 501 54.4 806 mg/kg rat 2,3,5-Trimethylpyrazine (chemical formula C7H10N2) is one of the most broadly used edible synthesis fragrances. It comes from baked food, fried barley, potatoes, and peanuts. 2,3,5-Trimethylpyrazine is used for the flavor in cocoa, coffee, chocolate, potato, cereal, and fried nuts. Physical properties The specific gravity depends on the quality and the producer and ranges from 0.967 to 0.987. Synthesis 2,3,5-Trimethylpyrazine can be synthesized from 2,3-butanedione and 1,2-diaminopropane. First, 1,2-diaminopropane is synthesized by amination of isopropanolamine in the presence of ammonia and a hydrogenation catalyst: Raney Ni. The effect of the amount of Raney Ni catalyst, the molar ratio of materials, reactions are as follows: the molar ratio of isopropanolamine to ammonia is 1:3.5, the reaction temperature is 160 °C, the reaction is 5 hours, the molar ratio of hydrogen to isopropanolamine is 1:5. Then the reaction consists of synthesis of 2,3,5-trimethyl-5,6-dihydropyrazine and 2,3,5-trimethylpyrazine. The optimum conditions of 2,3,5-trimethyl-5,6-dihydropropyrazine synthesis are established:2,3-butanedione which is mixed with anhydrous ethyl alcohol (the mass ratio of anhydrous ethyl alcohol to 2,3-butanedione was 5:1) is dropped to the mixture of anhydrous ethyl alcohol and 1,2-diaminopropane (the mass ratio of anhydrous ethyl alcohol to 1,2-diaminopropane was 6:1) at the even pace for four hours, the molar ratio of 2,3-butanedione to 1,2-diaminopropane is 1:1.1, the condensation reaction temperature is −5 °C. The best dehydrogen oxidation conditions are as follows: air is used as oxidant, the molar ration of potassium hydroxide and 2,3,5-Trimethyl-5,6-dihydro-pyrazine is 3:1, the mass ratio of ethanol to 2,3,5-trimethyl-5,6-dihydro-pyrazine 10:1, reaction temperature 68 °C, reaction time seven hours.2，3，5-三甲基吡嗪的合成研究 https://www.doc88.com/p-51076523314.html?r=1 Study on the synthesis of 2,3,5-trimethylpyrazine There are several other ways to synthesis 2,3,5-trimethylpyrazine: Piperazine gas phase catalytic dehydrogenation frameless|Piperazine gas phase catalytic dehydrogenation N-(β alkane alcohol)ethanediamine gas phase catalysis frameless|N-(β alkane alcohol)ethanediamine gas phase catalysis Ethanediamine and methyl aldehyde gas phase catalysis frameless|Ethanediamine and methyl aldehyde gas phase catalysis Diamine and diol gas phase catalysis frameless|Diamine and diol gas phase catalysis Use limit in food FEMA (mg/kg) Soft drinks 5.0～10 Candy 5.0～10 Baked food 5.0～10 Cereal 2.0 Seasoning 2.0 Meat 2.0 Dairy 1.0 Soup 2.0 References Additional references November 2021 2,3,5-三甲基吡嗪 | 14667-55-1 2me3me5me-pyrazine - Synthesis 14667-55-1, 2,3,5-trimethylpyrazine, CAS No 14667-55-1 2,3,5-trimethylpyrazine 2,3,5-三甲基吡嗪,14667-55-1，生产厂家，价格-lookchem 2，3，5-三甲基吡嗪的合成研究 2,3,5-trimethyl pyrazine, 14667-55-1 AIST:Spectral Database for Organic Compounds, SDBS https://web.archive.org/web/20100611030206/http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/direct_frame_top.cgi 2010-06-11 Category:Pyrazines