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Merck
CN

382000

4-羧基-TEMPO 自由基

97%

别名:

4-羧基-2,2,6,6-四甲基哌啶 1-氧基, 4-羧基-2,2,6,6-四甲基哌啶氧自由基, 4-羧基-TEMPO

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关于此项目

经验公式(希尔记法):
C10H18NO3
化学文摘社编号:
分子量:
200.25
UNSPSC Code:
12352000
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3949026
Assay:
97%
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InChI

1S/C10H18NO3/c1-9(2)5-7(8(12)13)6-10(3,4)11(9)14/h7H,5-6H2,1-4H3,(H,12,13)

SMILES string

CC1(C)CC(CC(C)(C)N1[O])C(O)=O

InChI key

CYQGCJQJIOARKD-UHFFFAOYSA-N

assay

97%

mp

185-189 °C (lit.)

functional group

carboxylic acid

storage temp.

2-8°C

Quality Level

General description

4-羧基-TEMPO 是 4-取代的 2,2,6,6-四甲基哌啶基-1-氧 (TEMPO) 衍生物。4-羧基-TEMPO 与 3-氨基丙基硅烷固定在介孔二氧化硅表面,组成多相催化系统,用于各种氧化反应。

Application

4-羧基-TEMPO 可用作将再生纤维素(粘胶纤维)氧化为纤维素酸的催化剂。

pictograms

Exclamation mark

signalword

Warning

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


历史批次信息供参考:

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Martina Schleicher et al.
International journal of biomaterials, 2012, 397813-397813 (2012-04-07)
In vivo self-endothelialization by endothelial cell adhesion on cardiovascular implants is highly desirable. DNA-oligonucleotides are an intriguing coating material with nonimmunogenic characteristics and the feasibility of easy and rapid chemical fabrication. The objective of this study was the creation of
G M Rosen et al.
Radiology, 163(1), 239-243 (1987-04-01)
The diagnosis of various disorders of the cerebrospinal fluid (CSF) with magnetic resonance (MR) imaging may require the intrathecal administration of a paramagnetic contrast agent. Furthermore, the CSF route provides direct access to the brain, circumventing the blood-brain barrier. Three
Dongxiao Wen et al.
International journal of analytical chemistry, 2018, 1710438-1710438 (2018-07-10)
A novel nanocomposite of nanoporous gold nanoparticles (np-AuNPs) functionalized with 2,2,6,6-tetramethyl-1-piperidinyloxy radical (TEMPO) was prepared; assembled carboxyl groups on gold nanoporous nanoparticles surface were combined with TEMPO by the "bridge" of carboxylate-zirconium-carboxylate chemistry. SEM images and UV-Vis spectroscopies of np-AuNPs
Fei Wang et al.
PloS one, 8(6), e64722-e64722 (2013-06-14)
In this study, the host-guest behavior of poly(amidoamine) (PAMAM) dendrimers bearing amine, hydroxyl, or carboxylate surface functionalities were investigated by paramagnetic NMR studies. 2,2,6,6-Tetramethylpiperidinyloxy (TEMPO) derivatives were used as paramagnetic guest molecules. The results showed that TEMPO-COOH significantly broaden the
Kazuyuki Hosokawa et al.
Free radical biology & medicine, 37(7), 946-952 (2004-09-01)
Three water-soluble carboxy nitroxide antioxidants, 5-carboxy-1,1,3,3-tetramethylisoindolin-2-yloxyl, 4-carboxy-2,2,6,6-tetramethylpiperidin-1-yloxyl, and 3-carboxy-2,2,5,5-tetramethylpyrrolidin-1-yloxyl, show significant impact on the postirradiation survival rates of ataxia telangiectasia (A-T) cells compared to normal cells, an assay which represents a model for understanding the impact of ROS damage on

商品

TEMPO(2,2,6,6-四甲基哌啶氧基或2,2,6,6-四甲基哌啶1-氧基)及其衍生物在有机氧化反应催化剂中可以作为稳定的硝酰基使用。TEMPO由Lebedev和Kazarnovskii于1960年发现,其具有的稳定自由基性质得益于其庞大的取代基团阻碍了自由基与其他分子之间发生反应。

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