Pyronin Y

Modify Date: 2024-01-01 17:51:07

Pyronin Y Structure
Pyronin Y structure
Common Name Pyronin Y
CAS Number 92-32-0 Molecular Weight 302.799
Density N/A Boiling Point N/A
Molecular Formula C17H19ClN2O Melting Point 250-260ºC(lit.)
MSDS Chinese USA Flash Point N/A

 Use of Pyronin Y


Pyronin Y is an intercalating cationic dye that shows specificity towards RNA.

 Names

Name acridine red 3B
Synonym More Synonyms

 Pyronin Y Biological Activity

Description Pyronin Y is an intercalating cationic dye that shows specificity towards RNA.
Related Catalog
In Vitro Pyronin Y forms fluorescent complexes with double-stranded nucleic acids, especially RNA, enabling semi-quantitative analysis of cellular RNA in flow cytometry, to estimate the RNA content per cell in formalin fixed EL4 leukosis tumor cells, enzyme dispersed R3327-G rat prostatic adenocarcinoma cells, mouse spleen cells stimulated with concanavalin A, and human peripheral blood lymphocytes stimulated with phytohemagglutinin[1]. A fluorescent staining procedure based on pyronin Y is described. The technique has been used to stain RNA in human reticulocytes for subsequent flow analysis and sorting[2]. In viable cells this dye also accumulates in mitochondria. At a concentration of 1.7 to 3.3 μM, pyronin Y is localized almost exclusively in mitochondria of cultured cells, similar to another mitochondria! probe, rhodamine 123. At that concentration PY is not toxic but suppressed cell growth, arresting cells[3]. Pyronin Y has long been used, in combination with other dyes such as Methyl Green, as a differential stain for nucleic acids in paraffin tissue sections. In sections stained with Methyl Green-pyronin Y, red blood cells, elastic fibre of blood vessels, zymogen granules of pancreatic acinar cells, surface membrane of heptocytes and kidney tubular cells showed strikingly strong green and/or red fluorescence, while the nuclei of cells appeared non-fluorescent[4].
Cell Assay The cells are resuspended and stained for 30 min in 1.0 mL of 0.01% pyronin Y in sodiumacetate buffer (1.0 M, pH 4.7). For this purpose 1.0 g of pyronin Y is dissolved in 100 mL distilled water and this solution is purified by chloroform extraction (three fractions of 100 mL). The purified pyronin Y solution is diluted with 1.0 M sodiumacetate buffer pH 4.7 to the appropriate concentration and filtered through paper filters before use. Stained cell samples are studied by fluorescence microscopy (excitation filters SP 560 and LP 515, chromatic beam splitter at 580 nm, barrier filter LP 580) or by flow cytometry[2].
References

[1]. Pollack A, et al. Flow cytometric analysis of RNA content in different cell populations using pyronin Yand methyl green. Cytometry. 1982 Jul;3(1):28-35.

[2]. Tanke HJ, et al. Flow cytometry of human reticulocytes based on RNA fluorescence. Cytometry. 1981 Mar;1(5):313-20.

[3]. Darzynkiewicz Z, et al. Cytostatic and cytotoxic properties of pyronin Y: relation to mitochondrial localization of the dye and its interaction with RNA. Cancer Res. 1986 Nov;46(11):5760-6.

[4]. Li B, et al. Pyronin Y as a fluorescent stain for paraffin sections. Histochem J. 2002 Jun-Jul;34(6-7):299-303.

 Chemical & Physical Properties

Melting Point 250-260ºC(lit.)
Molecular Formula C17H19ClN2O
Molecular Weight 302.799
Exact Mass 302.118591
PSA 19.39000
Storage condition Store at RT.
Water Solubility Soluble in water; sparingly soluble in ethanol, ethylene glycol, methyl cellosolve | Soluble in water. Also soluble in methyl cellosolve (9 mg/mL) and ethanol (3 mg/mL).

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
BQ1450000
CHEMICAL NAME :
Ammonium, (6-(dimethylamino)-3H-xanten-3-ylidene)dimethyl-, chloride
CAS REGISTRY NUMBER :
92-32-0
LAST UPDATED :
199701
DATA ITEMS CITED :
9
MOLECULAR FORMULA :
C17-H19-N2-O.Cl
MOLECULAR WEIGHT :
302.83
WISWESSER LINE NOTATION :
T C666 BO EYJ EUK1&1 MN1&1 &G

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
179 mg/kg
TOXIC EFFECTS :
Kidney, Ureter, Bladder - changes in tubules (including acute renal failure, acute tubular necrosis)

MUTATION DATA

TEST SYSTEM :
Insect - Drosophila melanogaster
DOSE/DURATION :
1000 ppm
REFERENCE :
AMNTA4 American Naturalist. (Univ. of Chicago Press, Journals Div., POB 37005, Chicago, IL 60637) V.1- 1867- Volume(issue)/page/year: 87,295,1953 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X7179 No. of Facilities: 63 (estimated) No. of Industries: 1 No. of Occupations: 3 No. of Employees: 1056 (estimated) No. of Female Employees: 810 (estimated)

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn: Harmful;
Risk Phrases R68
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS BQ1450000
HS Code 2921199090

 Customs

HS Code 2921199090
Summary 2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

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 Synonyms

N-[6-(dimethylamino)-3H-xanthen-3-ylidene]-N-methylmethanaminium chloride
Pyronine Y
Tetramethyl pyronin
EINECS 202-147-8
Ammonium, [6-(dimethylamino)-3H-xanthen-3-ylidene]dimethyl-, chloride
N-[6-(Dimethylamino)-3H-xanthene-3-ylidene]-N-methylmethanaminium Chloride
Pyronine
Methanaminium, N-[6-(dimethylamino)-3H-xanthen-3-ylidene]-N-methyl-, chloride (1:1)
Pyroniny(G)
Methyl pyronin
Pyronin G
Pyronine G chloride
Pyronine ZH
MFCD00011725
[6-(dimethylamino)xanthen-3-ylidene]-dimethylazanium,chloride
pyronine G hydrochloride
xanthylium, 3,6-bis(dimethylamino)-, chloride (1:1)
Xanthylium, 3,6-bis(dimethylamino)-, chloride
Pyronin Y
6-(Dimethylamino)-N,N-dimethyl-3H-xanthen-3-iminium chloride
Pyronine G
Pyronin Yellow
3,6-Bis(dimethylamino)xanthenium chloride
[6-(Dimethylamino)-3H-xanthen-3-ylidene]dimethylammonium Chloride
tetramethyldiaminoxanthylium chloride
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