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Acridine Orange base

Acridine Orange base structure

Acridine Orange base 

structure
  • CAS No:

    494-38-2

  • Formula:

    C17H19N3

  • Chemical Name:

    Acridine Orange base

  • Synonyms:

    3,6-Acridinediamine,N3,N3,N6,N6-tetramethyl-;Acridine,3,6-bis(dimethylamino)-;3,6-Acridinediamine,N,N,N′,N′-tetramethyl-;N3,N3,N6,N6-Tetramethyl-3,6-acridinediamine;C.I. 46005B;Brilliant Acridine Orange E;C.I. Solvent Orange 15;3,6-Di(dimethylamino)acridine;Waxoline Orange A;3,6-Bis(dimethylamino)acridine;Acridine Orange base;Acridine orange free base;NSC 194350;Solvent Orange 15;3-N,3-N,6-N,6-N-Tetramethylacridine-3,6-diamine

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

ChEBI: A member of the class of aminoacridines that is acridine carrying two dimethylamino substituents at positions 3 and 6. The hydrochloride salt is the fluorescent dye 'acridine orange', used for cell cycle determination.


Acridine orange free base is a member of the class of aminoacridines that is acridine carrying two dimethylamino substituents at positions 3 and 6. The hydrochloride salt is the fluorescent dye 'acridine orange', used for cell cycle determination. It has a role as a fluorochrome and a histological dye. It is a member of aminoacridines, an aromatic amine and a tertiary amino compound.|A cationic cytochemical stain specific for cell nuclei, especially DNA. It is used as a supravital stain and in fluorescence cytochemistry. It may cause mutations in microorganisms.

Acridine Orange base Basic Attributes

265.35

265.35

610-452-6

F30N4O6XVV

194350

DTXSID60197783

Characteristics

19.4

4.65

BROWN POWDER

1.2±0.1 g/cm3

181-182 °C

469℃

237℃

1.710

0.00 M

Subcutaneous-mouse LD50: 250 mg/kg

Flammable; burning produces toxic nitrogen oxide fumes

Safety Information

3

22-24/25

AR7600000

Treasury is ventilated, low temperature and dry; stored separately from food materials

Toxicity

highly toxic

Drug Information

Chemicals that emit light after excitation by light. The wave length of the emitted light is usually longer than that of the incident light. Fluorochromes are substances that cause fluorescence in other substances, i.e., dyes used to mark or label other compounds with fluorescent tags. (See all compounds classified as Fluorescent Dyes.)|Chemical agents that increase the rate of genetic mutation by interfering with the function of nucleic acids. A clastogen is a specific mutagen that causes breaks in chromosomes. (See all compounds classified as Mutagens.)

3,6-Bis(dimethylamino)acridine

Acridine Orange base Use and Manufacturing

A fluorescent nucleic acid binding dye which interacts with both DNA and RNA.

Computed Properties

Molecular Weight:265.35
XLogP3:3.4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:265.157897619
Monoisotopic Mass:265.157897619
Topological Polar Surface Area:19.4
Heavy Atom Count:20
Complexity:298
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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