Skip to Content
Merck
CN

A2145

Acridine hydrochloride

Synonym(s):

Acridine monohydrochloride, Acridinium chloride, acridin-10-ium chloride

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C13H9N · HCl
CAS Number:
Molecular Weight:
215.68
EC Number:
241-762-6
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
3697519
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


mp

250-255 °C (dec.)

solubility

H2O: soluble, methanol: soluble

SMILES string

Cl[H].c1ccc2nc3ccccc3cc2c1

InChI

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

InChI key

XUESTGHCVFYOLL-UHFFFAOYSA-N

Application

Acridine hydrochloride is a fluorescent compound with λexcitation and λemission of 355 nm and 440 nm, respectively. To investigate the release properties of multilayer nanocapsules, acridine hydrochloride has been utilized as a hydrophilic drug model and was loaded into the nano-structures .


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

target_organs

Respiratory system

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library



Yueheng Wu et al.
Orphanet journal of rare diseases, 15(1), 101-101 (2020-04-24)
Rubinstein-Taybi syndrome (RTS) is a rare, congenital, plurimalformative, and neurodevelopmental disorder. Previous studies have reported that large deletions contribute to more severe RTS phenotypes than those caused by CREBBP point mutations, suggesting a concurrent pathogenetic role of flanking genes, typical
Xue Gao et al.
Journal of medical genetics, 55(5), 298-306 (2018-02-18)
Background Hereditary sensorineural hearing loss is a genetically heterogeneous disorder. Objectives This study was designed to explore the genetic etiology of deafness in a large Chinese family with autosomal dominant, nonsyndromic, progressive sensorineural hearing loss (ADNSHL). Methods Whole exome sequencing
Jun Kawasaki et al.
The Journal of clinical investigation, 124(6), 2774-2784 (2014-05-20)
Vascular malformations are linked to mutations in RAS p21 protein activator 1 (RASA1, also known as p120RasGAP); however, due to the global expression of this gene, it is unclear how these mutations specifically affect the vasculature. Here, we tested the