跳转至内容
Merck
所有图片(4)

主要文件

查看所有文档

A23609

Sigma-Aldrich

吖啶

96.5 - 103.5% purity, powder or crystals

别名:

9-氮杂蒽；2,3-苯并喹啉

登录查看公司和协议定价
所有图片(4)

About This Item

经验公式（希尔记法）:
C13H9N
CAS号:
260-94-6
分子量:
179.22
Beilstein:
120200
EC 号:
205-971-6
MDL编号:
MFCD00005025
UNSPSC代码:
12171500
eCl@ss:
39210107
PubChem化学物质编号:
24890478
NACRES:
NA.47

产品名称

吖啶, ≥96.5% (HPLC)

质量水平

100

方案

≥96.5% (HPLC)
96.5-103.5% (perchloric acid titration)

表单

powder or crystals

技术

microbe id | staining: suitable

颜色

light beige to beige
light brown to brown
light yellow to very dark yellow

沸点

346 °C (lit.)

mp

107-110 °C (lit.)

λmax

392 nm

应用

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

SMILES字符串

c1ccc2nc3ccccc3cc2c1

InChI

1S/C13H9N/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-9H

InChI key

DZBUGLKDJFMEHC-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

一般描述

吖啶是一种小的阳离子平面染料，主要与RNA和DNA结合。具有强荧光性。结构与氧杂蒽类似，不过杂原子由氧换成氮。

应用

吖啶可染色核酸，尤其适合细胞周期研究。作为荧光材料，吖啶可用于生物分子可视化和激光领域。

象形图

Exclamation markEnvironment
GHS07,GHS09

警示用语：

Warning

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCL7134
BCCL9624
BCCL1910
BCCH2302
BCCJ5534

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

其他客户在看

Slide 1 of 4

1 of 4

吩嗪 98%

Sigma-Aldrich

P13207

吩嗪

9-氯吖啶 97%

Sigma-Aldrich

159425

9-氯吖啶

苯并[a]吖啶 BCR®, certified reference material

BCR157

苯并[a]吖啶

9-Methylacridine United States Pharmacopeia (USP) Reference Standard

USP

1424084

9-Methylacridine

Khaled Bodoor et al.
Journal of medicinal chemistry, 52(12), 3753-3761 (2009-05-19)
The design of RNA binding ligands is complicated by issues of specificity, target flexibility, and the tractability of known RNA inhibitors toward chemical derivitization. To address these difficulties, an RNA-directed fragment compound library is presented. We began with an analysis
Long N and Wong WT
The Chemistry of Molecular Imaging (2014)
Johannes Kornhuber et al.
European journal of medicinal chemistry, 44(6), 2667-2672 (2009-01-16)
We developed a structure-property-activity relationship (SPAR)-model for psychopharmacological drugs acting as non-competitive 5-HT(3A) receptor antagonists by using a decision-tree learner provided by the RapidMiner machine learning tool. A single molecular descriptor, namely the molecular dipole moment per molecular weight (mu/MW)
Mudit Tyagi et al.
Retrovirology, 12, 63-63 (2015-07-17)
HIV-1 escapes antiretroviral drugs by integrating into the host DNA and forming a latent transcriptionally silent HIV-1 provirus. This provirus presents the major hurdle in HIV-1 eradication and cure. Transcriptional activation, which is prerequisite for reactivation and the eradication of
Jiang-Wei Chen et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 34(4), 1175-1189 (2014-10-04)
Apoptosis and autophagy are two patterns of programmed cell death which play important roles in the intervertebral disc degeneration. Oxidative stress is an important factor for the induction of programmed cell death. However, the cellular reactions linking autophagy to apoptosis
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门