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1811-28-5

1811-28-5 Structure

1811-28-5 Structure
IdentificationBack Directory
[Name]

PROFLAVINE HEMISULFATE
[CAS]

1811-28-5
[Synonyms]

PROFLAVINE SULFATE
PROFLAVINE HEMISULFATE
PROFLAVINE HEMISULPHATE
3,6-DIAMINOACRIDINE SULFATE
PROFLAVINE HEMISULFATE SALT
2 8-DIAMINOACRIDINE SULFATE
PROFLAVINE HEMISULFATE HYDRATE
3,6-diamino-acridinsulfate(2:1)
3,6-DIAMINOACRIDINE HEMISULFATE
3,6-acridinediamine,sulfate(2:1)
3,6-DIAMINOACRIDINE HEMISULPHATE
proflavine hemisulfate salt hydrate
3,6-DIAMINOACRIDINE HEMISULFATE SALT
Proflavine hemisulfate salt dihydrate
Proflavine hydrate hemisulfate salt
PROFLAVINE HEMISULFATE SALT HYDRATE(RG)
3,6-DIAMINOACRIDINIUM MONOHYDROGEN SULFATE
3,6-Diaminoacridine hemisulfate, hydrate,98%
ProflavinrHemisulfateDihydrate(3,6-Diaminoacridi
PROFLAVINE HEMISULFATE DIHYDRATE, FOR FL UORESCENCE
3,6-Diaminoacridine monohydrochloride, Proflavine dihydrate hemisulfate salt
[EINECS(EC#)]

217-320-3
[Molecular Formula]

C26H24N6O4S
[MDL Number]

MFCD00013150
[MOL File]

1811-28-5.mol
[Molecular Weight]

516.57
Chemical PropertiesBack Directory
[Appearance]

orange to brown crystalline powder
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO (Slightly, Heated), Water (Slightly, Heated)
[form ]

powder
[color ]

Orange to Amber to Dark red
[PH]

pH (1g/l, 25℃) : 4.0~8.0
[Water Solubility ]

H2O: 10mg/mL
[BRN ]

3921806
[Stability:]

Hygroscopic
[EPA Substance Registry System]

3,6-Acridinediamine, sulfate (2:1) (1811-28-5)
Hazard InformationBack Directory
[Chemical Properties]

orange to brown crystalline powder
[Uses]

An Acridine derivative with limited antifungal activity
[Uses]

antiseptic
[Description]

Proflavine Hemisulfate, the hemisulfate form of proflavin, is an acridine-derived fluorescent contrast agent and disinfectant used for cell imaging and antiseptic purposes. Following topical application, proflavin diffuses into cells and intercalates into DNA, leading to its accumulation in and staining of the nucleus. This allows visualization of the nucleus during fluorescence imaging. Such capability enables nuclear morphometry and facilitates the identification of cancer cells. Additionally, proflavin sulfate exerts antimicrobial effects through binding to bacterial DNA, which disrupts DNA synthesis and inhibits bacterial cell growth.
[in vivo]

The concentrations of Proflavine (20 mg/kg) in whole blood after intravenous injection decreased rapidly at the beginning and remained stable from around 30 min after dosing[3].

Animal Model:Adult male Sprague Dawley rats (weighing approximately 200 g)[3]
Dosage:20 mg/kg (Pharmacokinetic Analysis)
Administration:Intravenous injection; 2, 4, 5, 10, 15, 20, 25, and 30 min after dosing
Result:Concentration decreased rapidly from whole blood in the first 5 min after dosing, followed by a slower decrease.
[Purification Methods]

An aqueous solution, after treatment with charcoal, is concentrated, chilled overnight, filtered and the precipitate is rinsed with a little diethyl ether. The precipitate is dried in air, then overnight in a vacuum oven at 70o. [Beilstein 22 I 650, 22/11 V 323.]
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[RTECS ]

AR9065100
[F ]

3-8-10-23
[HS Code ]

2918.19.9000
[Toxicity]

mouse,LD50,subcutaneous,200mg/kg (200mg/kg),Quarterly Journal of Pharmacy & Pharmacology. Vol. 10, Pg. 649, 1937.
Spectrum DetailBack Directory
[Spectrum Detail]

PROFLAVINE HEMISULFATE(1811-28-5)1HNMR
PROFLAVINE HEMISULFATE(1811-28-5)13CNMR
PROFLAVINE HEMISULFATE(1811-28-5)IR1
PROFLAVINE HEMISULFATE(1811-28-5)IR2
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