蒸汽密度
1.07 (vs air)
质量水平
蒸汽压
280 mmHg ( 20 °C)
659 mmHg ( 40 °C)
自燃温度
806 °F
浓度
40 wt. % in H2O
折射率
n20/D 1.37
bp
48 °C
密度
0.897 g/mL at 25 °C
SMILES字符串
CN
InChI
1S/CH5N/c1-2/h2H2,1H3
InChI key
BAVYZALUXZFZLV-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
甲胺溶液可以在牛奶和酸奶样本高氯酸盐分析作为LC-MS/MS移动相。
它可以用于以下反应合成:从丁香油酚生成
它可以用于以下反应合成:从丁香油酚生成
- 9-芴甲基N-氨基甲酸甲酯和叔-丁基N-氨基甲酸甲酯
- 7-氨基甲酸甲酯-2-(2-喹啉基)环庚三烯酮
- 2,5-内消旋-吡咯烷
- 2-(4-苯氯)-N-甲基乙酰胺
- 1,3-苯并恶嗪衍生物
警示用语:
Danger
危险分类
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 1
闪点(°F)
14.0 °F
闪点(°C)
-10 °C
个人防护装备
Faceshields, Gloves, Goggles
法规信息
易制爆化学品
危险化学品
Preparation of Tetrahydroisoquinoline-3-ones Via Cyclization of Phenyl Acetamides Using Eaton's Reagent.
Organic Syntheses, 44-54 (2012)
Nature communications, 10(1), 444-444 (2019-01-27)
Organic-inorganic metal halide perovskites have gained considerable attention for next-generation photovoltaic cells due to rapid improvement in power conversion efficiencies. However, fundamental understanding of underlying mechanisms related to light- and bias-induced effects at the nanoscale is still required. Here, structural
Orthogonally Protected N-Methyl-Substituted α-Aminoglycines.
Protein and peptide letters, 3(4), 219-224 (1996)
Organic & biomolecular chemistry, 10(35), 7148-7157 (2012-07-27)
Novel 2,5-meso-pyrrolidines have been straightforwardly synthesized from readily available symmetrical double Michael acceptors. The key step rested on an aza-Michael addition of primary alkylamines to bis-enones. Competitive Rauhut-Currier and aza-Michael reactions have been highlighted in protic solvent. Ultrasound activation associated
Nature, 550(7674), 92-95 (2017-09-05)
Recent advances in the use of organic-inorganic hybrid perovskites for optoelectronics have been rapid, with reported power conversion efficiencies of up to 22 per cent for perovskite solar cells. Improvements in stability have also enabled testing over a timescale of
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门