128759
6-羟基哌啶-3-羧酸
98%
别名:
2-羟基-5-吡啶羧酸, 6-羟基烟酸
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关于此项目
经验公式（希尔记法）:
C6H5NO3
化学文摘社编号:
分子量:
139.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-682-9
Beilstein/REAXYS Number:
115991
MDL number:
Assay:
98%
Form:
powder
InChI key
BLHCMGRVFXRYRN-UHFFFAOYSA-N
InChI
1S/C6H5NO3/c8-5-2-1-4(3-7-5)6(9)10/h1-3H,(H,7,8)(H,9,10)
SMILES string
OC(=O)c1ccc(O)nc1
assay
98%
form
powder
mp
>300 °C (lit.)
functional group
carboxylic acid
Quality Level
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General description
6-羟基吡啶-3-羧酸（6-羟基烟酸）与 Ln(2)O(3) (Ln = Nd、Sm、Eu、Gd) 和草酸 (H(2)OX) 反应生成四种新型镧系元素 -有机配位聚合物网络。
Application
6-羟基吡啶-3-羧酸（6-羟基烟酸）用于合成分子印迹聚合物（MIP）。。
用于类维生素A的合成。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Synthesis, 285-285 (1995)
Cai-Ming Liu et al.
Dalton transactions (Cambridge, England : 2003), (29)(29), 5666-5672 (2010-05-08)
6-Hydroxypyridine-3-carboxylic acid (6-HOPy-3-CO(2)H) reacts with Ln(2)O(3) (Ln = Nd, Sm, Eu, Gd) and oxalic acid (H(2)OX) under hydrothermal conditions to generate four novel lanthanide-organic coordination polymeric networks [Ln(2)(1H-6-Opy-3-CO(2))(2)(OX)(2)(H(2)O)(3)] x 2.5 H(2)O (Ln = Nd, 1; Sm, 2; 1H-6-Opy-3-CO(2)(-) = 1-hydro-6-oxopyridine-3-carboxylate)
Dayun Zhao et al.
Analytical and bioanalytical chemistry, 401(7), 2259-2273 (2011-08-27)
A new molecularly imprinted polymer (MIP) has been prepared on silica beads using the radical "grafting from" polymerization method for selective extraction of minor contaminant mycotoxin of patulin (PTL). After the introduction of amino groups onto the silica surface with
Li Xu et al.
Wei sheng wu xue bao = Acta microbiologica Sinica, 46(1), 63-67 (2006-04-04)
The current technology for microbial hydroxylation of nicotinic acid is a procedure of resting cells transformation. Here it was reported that non-degradation of 6-hydroxynicotinic acid during hydroxylation of nicotinic acid by resting cells was due to existing of nicotinic acid
Ashish Gupta et al.
NMR in biomedicine, 18(5), 293-299 (2005-03-11)
The utility of (1)H NMR spectroscopy is suggested and demonstrated for the diagnosis of Pseudomonas aeruginosa in urinary tract infection (UTI). The specific property of P. aeruginosa of metabolizing nicotinic acid to 6-hydroxynicotinic acid (6-OHNA) is exploited. The quantity of
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