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Merck
CN
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文件

Q2876

Sigma-Aldrich

喹吖因氮芥 二盐酸盐

≥85% (HPLC)

别名:

氮芥喹丫因 二盐酸盐, 氮芥喹丫因 二盐酸盐 二盐酸盐

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About This Item

经验公式（希尔记法）:
C23H28Cl3N3O · 2HCl
CAS号:
4213-45-0
分子量:
541.77
Beilstein:
3819822
EC 号:
224-140-9
MDL编号:
MFCD00043254
UNSPSC代码:
12352101
PubChem化学物质编号:
24899329
NACRES:
NA.32

质量水平

200

检测方案

≥85% (HPLC)

储存温度

−20°C

SMILES字符串

Cl[H].Cl[H].COc1ccc2nc3cc(Cl)ccc3c(NC(C)CCCN(CCCl)CCCl)c2c1

InChI

1S/C23H28Cl3N3O.2ClH/c1-16(4-3-11-29(12-9-24)13-10-25)27-23-19-7-5-17(26)14-22(19)28-21-8-6-18(30-2)15-20(21)23;;/h5-8,14-16H,3-4,9-13H2,1-2H3,(H,27,28);2*1H

InChI key

JETDZFFCRPFPDH-UHFFFAOYSA-N

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一般描述

氮芥喹丫因（Quinacrine mustard dihydrochloride） 是一种荧光吖啶染料，简称QM。在水溶液中，氯乙基迅速失去氯离子，产生氮丙啶阳离子。这些阳离子很容易与蛋白质和核酸的羧基、硫醇和杂环氮基团或其他亲核试剂发生反应。

应用

氮芥喹丫因（Quinacrine mustard dihydrochloride）用于染色中期染色体。最新应用包括玉米的 Q 带分析和鱼类的核型分析。该染料还用作锥虫的活体染色剂。

象形图

Skull and crossbonesHealth hazard
GHS06,GHS08

警示用语：

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Repr. 2 - Resp. Sens. 1 - Skin Sens. 1

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

分析证书(COA)

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. Is quinacrine mustard, product Q2876, suitable as a viability stain for platelets?

    A customer's feedback utlizing the method outlined in Moroi, M. et al., Blood, 88(6), 2081-2092 (1996), stated it performed pretty well, giving a strong green signal using a standard GFP-filter.

  6. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Michiko Inuma et al.
Zoological science, 24(6), 588-595 (2007-09-18)
"Delayed QM-fluorescence" refers to the unusual kinetics of fluorescence from most of the C-heterochromatic regions of the chromosomes of the small Japanese field mouse Apodemus argenteus. When stained with quinacrine mustard (QM-stained), these C-heterochromatic regions emit weak fluorescence immediately after
Monika Pietrzak et al.
Biophysical chemistry, 104(1), 305-313 (2003-07-02)
The present study was designed to estimate the ability of chlorophyllin (CHL) to interact with two acridine mutagens, quinacrine mustard (QM) and acridine orange (AO), and with the antitumor anthracycline doxorubicin (Dox). To this end, aqueous solutions of QM, AO
B Ardelt et al.
International journal of oncology, 18(4), 849-853 (2001-03-17)
Chlorophyllin (CHL), the sodium and copper salt of chlorophyll, is capable of inhibiting the mutagenic activity of many chemical compounds. Several mechanisms have been advanced to explain the antimutagenic activity of CHL, including its antioxidant properties and its ability to
Y Obara et al.
Zoological science, 14(1), 57-64 (1997-02-01)
The small Japanese field mouse Apodemus argenteus has the diploid chromosome number of 46, carrying rather large centromeric C-heterochromatin in most of the 44 autosomes and a large amount of C-heterochromatin in the sex chromosomes: the largest subtelocentric X was
Ahilan Saravanamuthu et al.
The Journal of biological chemistry, 279(28), 29493-29500 (2004-04-23)
Trypanothione reductase is a key enzyme in the trypanothione-based redox metabolism of pathogenic trypanosomes. Because this system is absent in humans, being replaced with glutathione and glutathione reductase, it offers a target for selective inhibition. The rational design of potent
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