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408166

Sigma-Aldrich

1-(2-吡啶基)哌嗪

≥99%

别名:

2-哌嗪吡啶

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5 ML
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25 ML
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About This Item

经验公式（希尔记法）:
C9H13N3
CAS号:
34803-66-2
分子量:
163.22
Beilstein:
140423
EC 号:
252-220-3
MDL编号:
MFCD00006216
UNSPSC代码:
12352100
PubChem化学物质编号:
24865508
NACRES:
NA.22

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质量水平

100

方案

≥99%

表单

liquid

折射率

n20/D 1.595 (lit.)

沸点

120-122 °C/2 mmHg (lit.)

密度

1.072 g/mL at 25 °C (lit.)

SMILES字符串

C1CN(CCN1)c2ccccn2

InChI

1S/C9H13N3/c1-2-4-11-9(3-1)12-7-5-10-6-8-12/h1-4,10H,5-8H2

InChI key

GZRKXKUVVPSREJ-UHFFFAOYSA-N

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一般描述

1-（2-吡啶基）哌嗪是一种哌嗪衍生物。

应用

1-（2-吡啶基）哌嗪可作为反相 HPLC 测定空气中脂肪族和芳香族异氰酸酯的试剂。[1][2] 可作为空气中二异氰酸酯荧光测定的试剂。[3]

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

230.0 °F - closed cup

闪点(°C)

110 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCV7943
MKCS3791
MKCM0282
MKCG0799
MKBZ2433V

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Determination of atmospheric isocyanate concentrations by high-performance thin-layer chromatography using 1-(2-pyridyl) piperazine reagent.
Ellwood PA, et al.
Analyst, 106(1258), 85-93 (1981)
Determination of trace atmospheric isocyanate concentrations by reversed-phase high-performance liquid chromatography using 1-(2-pyridyl) piperazine reagent.
Goldberg PA, et al.
Journal of Chromatography A, 212(1), 93-104 (1981)
Absorption and fluorescence of 1-(2-pyridyl)-piperazine and four diisocyanate derivatives in solution.
Salthammer T, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 107(1), 159-164 (1997)
Harvey Wong et al.
Drug metabolism and disposition: the biological fate of chemicals, 35(8), 1387-1392 (2007-05-15)
The pharmacokinetics and in vivo potency of 6-hydroxybuspirone (6-OH-buspirone), a major metabolite of buspirone, were investigated. The plasma clearance (47.3 +/- 3.5 ml/min/kg), volume of distribution (2.6 +/- 0.3 l/kg), and half-life (1.2 +/- 0.2 h) of 6-OH-buspirone in rats
Robert Lavieri et al.
Bioorganic & medicinal chemistry letters, 19(8), 2240-2243 (2009-03-21)
This Letter describes the synthesis and structure-activity relationships (SAR) of isoform-selective PLD inhibitors. By virtue of the installation of a 1,3,8-triazaspiro[4,5]decan-4-one privileged structure, PLD inhibitors with nanomolar potency and an unprecedented 40-fold selectivity for PLD2 over PLD1 were developed. Interestingly
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