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%
refractive index
n20/D 1.498 (lit.)
bp
171-172 °C (lit.)
mp
−43 °C (lit.)
density
0.917 g/mL at 25 °C (lit.)
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
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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
Halogen complexes. III. The association of 2, 4, 6-trimethylpyridine and trifluoroiodomethane.
Larsen DW and Allred AL.
The Journal of Physical Chemistry, 69(7), 2400-2401 (1965)
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
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
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