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1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐

更新时间:2025-08-25 10:43:40

1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐结构式
1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐结构式
品牌特惠专场
常用名 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐 英文名 4-Piperidone, 1-hydroxy-2,2,6,6-tetramethyl
CAS号 3637-11-4 分子量 171.23700
密度 1.02g/cm3 沸点 257.5ºC at 760mmHg
分子式 C9H17NO2 熔点 N/A
MSDS N/A 闪点 109.5ºC

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐用途


Tempone-H可用作化学和生物系统中的自旋陷阱,以量化过亚硝酸根和超氧自由基的形成。铁离子和铜离子是Tempone-H[1][2]的有效氧化剂。

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐名称

中文名 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐
英文名 1-hydroxy-2,2,6,6-tetramethylpiperidin-4-one
英文别名 更多

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐生物活性

描述 Tempone-H可用作化学和生物系统中的自旋陷阱,以量化过亚硝酸根和超氧自由基的形成。铁离子和铜离子是Tempone-H[1][2]的有效氧化剂。
相关类别
体外研究 使用TEMPONE-H检测过氧亚硝酸盐或超氧自由基的灵敏度约为使用自旋陷阱DMPO或TMIO的10倍[1]。
参考文献

[1]. Dikalov S, et al. Quantification of peroxynitrite, superoxide, and peroxyl radicals by a new spin trap hydroxylamine 1-hydroxy-2,2,6,6-tetramethyl-4-oxo-piperidine. Biochem Biophys Res Commun. 1997 Jan 3;230(1):54-7.

[2]. Dikalov SI, et al. Amyloid beta peptides do not form peptide-derived free radicals spontaneously, but can enhance metal-catalyzed oxidation of hydroxylamines to nitroxides. J Biol Chem. 1999 Apr 2;274(14):9392-9.

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐物理化学性质

密度 1.02g/cm3
沸点 257.5ºC at 760mmHg
分子式 C9H17NO2
分子量 171.23700
闪点 109.5ºC
精确质量 171.12600
PSA 40.54000
LogP 1.53560
InChIKey KMEUSKGEUADGET-UHFFFAOYSA-N
SMILES CC1(C)CC(=O)CC(C)(C)N1O
储存条件 -20°C

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐安全信息

海关编码 2933399090

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐合成线路

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐海关

海关编码 2933399090
中文概述 2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐靶点实验

查看更多实验

实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4296184
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
实验名称:Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
来源:ChEMBL
靶标:Escherichia coli
External Id:CHEMBL4296185
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐英文别名

1-hydroxy-2,2,6,6-tetramethyl-piperidin-4-one
1-Hydroxy-2,2,6,6-tetramethyl-4-oxopiperidine
4-oxo-TEMPO-H
4-Piperidinone,1-hydroxy-2,2,6,6-tetramethyl
1-Hydroxy-2,2,6,6-tetramethyl-piperidin-4-on
2,2,6,6-tetramethyl-4-oxo-1-piperidinyloxy
Tempone-H
N-hydroxy-4-oxo-2,2,6,6-tetramethylpiperidine
1-Hydroxy-2,2,6,6-tetramethyl-4-piperidinone
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