Skip to Content
Merck
All Photos(4)

Documents

A23609

Sigma-Aldrich

Acridine

96.5 - 103.5% purity, powder or crystals

Synonym(s):

9-Azaanthracene; 2,3-Benzoquinoline

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C13H9N
CAS Number:
260-94-6
Molecular Weight:
179.22
Beilstein:
120200
EC Number:
205-971-6
MDL number:
MFCD00005025
UNSPSC Code:
12171500
eCl@ss:
39210107
PubChem Substance ID:
24890478
NACRES:
NA.47

product name

Acridine, ≥96.5% (HPLC)

Quality Level

100

Assay

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

form

powder or crystals

color

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

bp

346 °C (lit.)

mp

107-110 °C (lit.)

λmax

392 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

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

Looking for similar products? Visit Product Comparison Guide

General description

Acridine is a small cationic and planar dye that mainly binds to RNA and DNA. These dyes are strongly fluorescent. It resembles the structure of xanthene except that the heteroatom is nitrogen, not oxygen.

Application

Acridine is suitable for nucleic acid staining, particularly for cell cycle determination. Acridines are used as fluorescent materials for visualization of biomolecules, and in laser technologies.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335,H410

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL7134
BCCL9624
BCCL1910
BCCH2302
BCCJ5534

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 4

1 of 4

Phenazine 98%

Sigma-Aldrich

P13207

Phenazine

9-Chloroacridine 97%

Sigma-Aldrich

159425

9-Chloroacridine

Benz[a]acridine BCR®, certified reference material

BCR157

Benz[a]acridine

9-Methylacridine United States Pharmacopeia (USP) Reference Standard

USP

1424084

9-Methylacridine

Long N and Wong WT
The Chemistry of Molecular Imaging (2014)
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
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)
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service