选用24%氨氯吡啶酸水剂对灌木进行对照试验。
The controlling test was carried out to the shrub with 24% picloram.
甲氨喋呤加柳氮磺吡啶疗法是推荐给那些患病时间长久，病情高度活动、但是没有不良预后特征的患者。
Methotrexate plus sulfasalazine is recommended in patients with all disease durations provided they have high disease activity and poor prognostic features.
用氟硅酸铵对HMCM-22分子筛进行了改性处理，并采用氨程序升温脱附和吡啶吸附红外光谱法测定了其酸性。
HMCM-22 zeolite was modified with ammonium hexafluorosilicate and characterized by temperature-programmed desorption of ammonia and pyridine adsorption infrared spectroscopy.
本文介绍的基于氨氧化法生产烟酸的工艺，选择了适当的复合催化剂，使原料3-甲基吡啶转化率可达99％，技术水平达到国外先进水平。
The manufacture process of nicotinic acid based on ammonia oxidation method, which is introduced in this article, reached 99% conversion of 3-methyl pyridine.
吡啶碱的生产方法主要有两种：一是从煤焦油中提取；二是从氨和甲醛、乙醛的合成过程中获得。
There are two manufacturing methods of pyridine bases: extraction from coal tar and catalytic synthesis from ammonia, formaldehyde and acetaldehyde.
本发明公开了一种2 -氨甲基吡啶镍配合物及其制备方法和应用。
The invention discloses a 2-ammonia methyl-pyridine nickel composition, a preparation method and the application thereof.
氨氯地平是新型二氢吡啶类钙通道阻滞剂。
Amlodipine (ALDP) is a new kind of calcium channel blocker of dihydropyridine.
本文报道四组降压药对血脂代谢的影响，研究发现氨苯喋啶、硝苯吡啶对血脂代谢无不良影响。
This article reports the result of a clinical study on the effect of four groups of antihypertensive drugs on blood lipids metabolism.
选用24%氨氯吡啶酸水剂，对林地一年生及多年生阔叶杂草、灌木进行防除试验。
The controlling test was carried out to the annual and perennial broadleaved weed and shrub on forestland with 24% picloram Sc.
以4甲基吡啶为原料，在固定床反应器中通过含氧化钒的催化剂发生气固相接触氨氧化反应制备雷米封中间体4氰基吡啶，4甲基吡啶的转化率为99%，4氰基吡啶的选择性为88%，收率为87。
4-cyanopyridine, intermediate of rimifon, was synthesized from 4-picoline using vanadium oxide as a catalyst in a fixed-bed reactor, reached 99% conversion of 4-picoline, 88% selectivity and 87.
以4甲基吡啶为原料，在固定床反应器中通过含氧化钒的催化剂发生气固相接触氨氧化反应制备雷米封中间体4氰基吡啶，4甲基吡啶的转化率为99%，4氰基吡啶的选择性为88%，收率为87。
4-cyanopyridine, intermediate of rimifon, was synthesized from 4-picoline using vanadium oxide as a catalyst in a fixed-bed reactor, reached 99% conversion of 4-picoline, 88% selectivity and 87.
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