142387
2,4,6-三甲基吡啶
99%, liquid, ReagentPlus®
别名:
2,4,6-三甲基氮杂苯, 对称-三甲基吡啶
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关于此项目
经验公式（希尔记法）:
C8H11N
化学文摘社编号:
分子量:
121.18
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-613-3
MDL number:
Beilstein/REAXYS Number:
107283
Assay:
99%
Form:
liquid
产品名称
2,4,6-三甲基吡啶, ReagentPlus®, 99%
InChI key
BWZVCCNYKMEVEX-UHFFFAOYSA-N
InChI
1S/C8H11N/c1-6-4-7(2)9-8(3)5-6/h4-5H,1-3H3
SMILES string
Cc1cc(C)nc(C)c1
product line
ReagentPlus®
assay
99%
form
liquid
Quality Level
bp
171-172 °C (lit.)
mp
−43 °C (lit.)
density
0.917 g/mL at 25 °C (lit.)
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General description
2,4,6-三甲基吡啶是一种吡啶衍生物。它具有7.4的pK。该产物可与环戊烷溶液中的三氟碘甲烷反应生成1:1的络合物。可通过NMR（核磁共振）光谱对该络合物进行研究。通过向其中加入四氧化锇溶液来制备可力丁缓冲的四氧化锇溶液。这些溶液已被用作电子显微镜研究的固定剂。
2,4,6-三甲基吡啶可用高锰酸钾氧化形成2,4,6-吡啶三羧酸。
2,4,6-三甲基吡啶可用高锰酸钾氧化形成2,4,6-吡啶三羧酸。
受阻的基底。
Application
2,4,6-三甲基吡啶（可力丁，s-可力丁，2,4,6-可力丁）已被用于制备带有低分子量N-酰基的N-酰基氨基香豆素的文库。
可用于通过无水碘化锂裂解位阻酯的有用溶剂。
用作电子显微镜的组织固定剂。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
131.0 °F - closed cup
flash_point_c
55 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Synthesis, structure, photoluminescence and magnetic properties of new 3-D lanthanide-pyridine-2, 4, 6-tricarboxylate frameworks
Li C-J, et al.
CrystEngComm, 10(11), 1645-1652 (2008)
Andrew W Patterson et al.
Nature protocols, 2(2), 424-433 (2007-04-05)
Substrate activity screening (SAS) is a fragment-based method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. The method consists of three steps: (i) a library of N-acyl aminocoumarins with diverse
Leszek Pazderski et al.
Magnetic resonance in chemistry : MRC, 48(6), 417-426 (2010-05-18)
(1)H, (13)C and (15)N NMR studies of gold(III), palladium(II) and platinum(II) chloride complexes with dimethylpyridines (lutidines: 2,3-lutidine, 2,3lut; 2,4-lutidine, 2,4lut; 3,5-lutidine, 3,5lut; 2,6-lutidine, 2,6lut) and 2,4,6-trimethylpyridine (2,4,6-collidine, 2,4,6col) having general formulae [AuLCl(3)], trans-[PdL(2)Cl(2)] and trans-/cis-[PtL(2)Cl(2)] were performed and the respective
Janet E Del Bene et al.
The journal of physical chemistry. A, 110(3), 1128-1133 (2006-01-20)
Ab initio EOM-CCSD calculations have been performed on 3:1 FH:NH3 complexes at their own optimized MP2/6-31+G(d,p) geometries and at the optimized geometries in the hydrogen-bonding regions of corresponding 3:1 FH:collidine complexes. The isolated gas-phase equilibrium 3:1 FH:NH3 complex has an
J L Tomsig et al.
Histochemistry, 89(3), 301-306 (1988-01-01)
In previous work of our laboratory it was demonstrated that collidine (2,4,6-trimethylpyridine) abolishes the core osmiophilia and chromaffin reaction from rat pinal gland and vas deferens nerves. This abolition was apparent when tissues were briefly incubated in collidine or when
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