Propidium iodide(PI) - ≥98%(HPLC) , CAS No.25535-16-4

CAS: 25535-16-4 Cat. No.: P266304 Fórmula: C27H34I2N4 Peso molecular: 668.39 Beilstein Registry Number: 3843838 Número EC: 247-081-0 PubChem CID: 104981
Disponible para pedir
GRADE & PURITY ≥98%(HPLC)
Synonyms
2,7-Diamino-9-phenyl-10 (diethylaminopropyl)-phenanthridium iodide methiodide | HMS3403D19 | Propidium Iodine | 3,8-Diamino-5-[3-(diethylmethylammonio)propyl]-6-phenylphenanthridinium diiodide | 3,8-Diamino-5-(3-(diethylmethylammonio)propyl)-6-phenylphena
Storage
Protected from light,Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
★
Size
Alemania (EU)
USA*
Price
Qty
5mg
P266304-5mg
—
3 Disponible
14,66€
25mg
P266304-25mg
—
2 Disponible
43,30€
100mg
P266304-100mg
—
2 Disponible
121,40€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C,Desiccated Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 279 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

PI is a nuclear staining reagent that can stain DNA. Like EB, PI intercalates into double-stranded DNA and releases red fluorescence. It is often used for the detection of apoptosis or necrosis, and is often used for flow cytometry analysis. Although PI cannot pass through living cell membranes, it can pass through damaged cell membranes to stain nuclei. PI is often used with Calcein, AM, Hoechst 33258 or Hoechst 33342, etc. It can stain live and dead cells at the same time. The excitation and emission wavelengths of the PI-DNA complex are 535nm and 615nm, respectively.

Dyeing process

(1) Prepare 10-50μM PI solution with PBS or appropriate buffer.

(2) Add 1/10 of the volume of the medium to the cell culture medium (1/10 concentration of PI buffer can also be used to replace the medium).

(3) Incubate the cells at 37°C for 10-20 minutes.

(4) Wash the cells twice with PBS or a suitable buffer.

(5) Observe the cells with a fluorescence microscope with a 535nm excitation wavelength and a 615nm emission wavelength filter.

Storage conditions: Store at -20°C dry and dark, valid for one year.
Precautions

MSDS shows that propidium iodide PI is the same as EB mutagenic to germ cells and is a carcinogen. Please take strict care to protect it!

Propidium iodide PI is a Germ cell mutagenicity germ cell mutant; In vitro tests showed mutagenic effects!

Specifications

Sinónimos
2,7-Diamino-9-phenyl-10 (diethylaminopropyl)-phenanthridium iodide methiodide | HMS3403D19 | Propidium Iodine | 3,8-Diamino-5-[3-(diethylmethylammonio)propyl]-6-phenylphenanthridinium diiodide | 3,8-Diamino-5-(3-(diethylmethylammonio)propyl)-6-phenylphena
Especificaciones y pureza
≥98%(HPLC)
Condiciones de almacenamiento de almacenamiento
Protected from light,Store at -20°C,Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%(HPLC)
Nombres e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504756593
Sonrisas canónicas
CC[N+](C)(CC)CCC[N+]1=C2C=C(C=CC2=C3C=CC(=CC3=C1C4=CC=CC=C4)N)N.[I-].[I-]
IUPAC Name
3-(3,8-diamino-6-phenylphenanthridin-5-ium-5-yl)propyl-diethyl-methylazanium;diiodide
InChIKey
XJMOSONTPMZWPB-UHFFFAOYSA-M
INCHI
1S/C27H33N4.2HI/c1-4-31(3,5-2)17-9-16-30-26-19-22(29)13-15-24(26)23-14-12-21(28)18-25(23)27(30)20-10-7-6-8-11-20;;/h6-8,10-15,18-19,29H,4-5,9,16-17,28H2,1-3H3;2*1H/q+1;;/p-1
Isómeros SMILES
CC[N+](C)(CC)CCC[N+]1=C2C=C(C=CC2=C3C=CC(=CC3=C1C4=CC=CC=C4)N)N.[I-].[I-]
WGK Alemania
3
RTECS
SF7949600
PubChem CID
104981
Peso molecular
668.39
Beilstein
3843838

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseQuinolines and derivatives
SubclassPhenylquinolines
Intermediate Tree Nodes Not available
Direct ParentPhenylquinolines
Alternative Parents Phenanthridines and derivatives  Phenylpyridines  Isoquinolines and derivatives  Benzene and substituted derivatives  Tetraalkylammonium salts  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organic iodide salts  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phenylquinoline - Benzoquinoline - Phenanthridine - 2-phenylpyridine - Isoquinoline - Monocyclic benzene moiety - Benzenoid - Pyridine - Tetraalkylammonium salt - Heteroaromatic compound - Quaternary ammonium salt - Azacycle - Organic salt - Organic iodide salt - Amine - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Primary amine - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.
External Descriptors organic iodide salt
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BACE1 Tchem Beta-secretase 1 (15641 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Cholinesterases; ACHE & BCHE (1222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)
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Plasmodium falciparum (966862 Activities)
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Calf thymus DNA (4845 Activities)
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GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

32 results found

Lot NumberCertificate TypeFechaArticulo
I2615772Certificate of AnalysisSep 11, 2026 P266304
I2615771Certificate of AnalysisSep 11, 2026 P266304
I2615770Certificate of AnalysisSep 11, 2026 P266304
I2615768Certificate of AnalysisSep 11, 2026 P266304
I2610713Certificate of AnalysisSep 11, 2026 P266304
J2214030Certificate of AnalysisSep 07, 2026 P266304
K2511576Certificate of AnalysisAug 04, 2026 P266304
K2511575Certificate of AnalysisAug 04, 2026 P266304
K2511558Certificate of AnalysisAug 04, 2026 P266304
G2327037Certificate of AnalysisAug 04, 2026 P266304
J2214031Certificate of AnalysisJul 03, 2026 P266304
H2515096Certificate of AnalysisMay 20, 2026 P266304
A2404015Certificate of AnalysisApr 03, 2026 P266304
K2317040Certificate of AnalysisMar 18, 2026 P266304
C2617297Certificate of AnalysisMar 14, 2026 P266304
C2617296Certificate of AnalysisMar 14, 2026 P266304
H2405417Certificate of AnalysisFeb 05, 2026 P266304
H2405421Certificate of AnalysisFeb 05, 2026 P266304
F2625064Certificate of AnalysisJan 10, 2026 P266304
A2613621Certificate of AnalysisJan 10, 2026 P266304
A2613630Certificate of AnalysisJan 10, 2026 P266304
A2613623Certificate of AnalysisJan 10, 2026 P266304
A2613622Certificate of AnalysisJan 10, 2026 P266304
K2511574Certificate of AnalysisNov 07, 2025 P266304
A2404014Certificate of AnalysisJul 10, 2025 P266304
E2416301Certificate of AnalysisMar 04, 2025 P266304
H2405419Certificate of AnalysisJul 31, 2024 P266304
E2416283Certificate of AnalysisMay 13, 2024 P266304
E2416299Certificate of AnalysisMay 13, 2024 P266304
L2325053Certificate of AnalysisJan 03, 2024 P266304
J2310198Certificate of AnalysisJul 13, 2023 P266304
J2214036Certificate of AnalysisJul 13, 2023 P266304
Propiedades químicas y físicas
SensibilidadLight sensitive;Moisture sensitive
Punto de fusión (°C)220-225°C
Peso molecular668.400 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass668.087 Da
Monoisotopic Mass668.087 Da
Topological Polar Surface Area55.900 Ų
Heavy Atom Count33
Formal Charge0
Complexity555.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Preguntas frecuentes y artículos
Annexin V-FITC staining to detect cell apoptosis
In Vitro Cytotoxicity Testing Guide
EdU Cell Proliferation Assay Kit
Cell Live/Dead Staining and Apoptosis Detection Techniques
A Comprehensive Overview of Zinc Ion Fluorescent Probes: From TSQ / Zinquin to ZnAF / Zinpyr-1 – Mechanistic Comparison and Aladdin Selection Guide
Fluorescent Probes: A Complete Beginner’s Guide — Definitions & Emission Mechanisms, Signal Readouts, Classification Framework, Selection Roadmap, and Product Tables (Tables 1–4)
16 Frequently Asked Questions About Nourseothricin
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Comparative Guide and Selection Framework for Common Fluorophores
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Glutaraldehyde-mediated Microbial Inactivation: Chemical Mechanisms, Determinants, and Key Validation Considerations
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The Key Starting Point for Phosphatidylserine Research: Changes in Membrane Localization, Functional Shifts, and Interpretation of Findings
Standard Operating Procedure for SYTO 9 and PI Combined Live/Dead Staining
Comparative Analysis and Selection Strategies for Mounting Media in Immunological Experiments
Cell Apoptosis Detection by TUNEL Labeling: Signal Interpretation and Result Evaluation
Application Comparison of the Neutral Red Assay and the MTT/CCK-8 Assays in Cytotoxicity Testing
Fluorescent Dyes in Life Science Research: Classification, Labeling Principles, and Experimental Applications
Comparison of Common Mammalian Cell Antibiotic Selection Systems: Puromycin, G418, Hygromycin B, and Blasticidin
Construction and Evaluation Strategy of a Gentamicin-Induced Cell Injury Model
Types, Binding Mechanisms, and Experimental Selection of Nuclear Dyes
Neuropathological Mechanisms of Cerebral Infarction
Research on Cell Cycle and DNA Damage Response Mechanisms
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Summary of Cell Staining Methods
Molecular Mechanisms, Detection Methods, and Disease Research Applications of Pyroptosis
Mechanisms of Action, Representative Compounds, and Research Applications of Senolytics
Turning “Cold” Tumors “Hot”: Immune Activation Mechanisms and Intervention Strategies
Renal Tubule-Associated Urinary Proteins: Sources, Mechanisms of Change, and Applications in Kidney Injury Research
Necroptosis and Tumor Immunity: The RIPK1–RIPK3–MLKL Axis, ZBP1 Signaling, and Experimental Determination
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Dual Vulnerabilities of MSI-H Tumors: Immune Responses and Synthetic Lethality with WRN
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ADAR1: A Potential Target in Tumor Immunity
Citations of This Product
Calculadoras de soluciones
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