Nuclear Fast Red Staining Solution - BioReagent, Biological Stain, for microscopy, 0.1% , CAS No.6409-77-4

CAS: 6409-77-4 Cat. No.: N743376 Molecular Weight: 357.28 EC Number: 229-088-0
AVAILABLE TO ORDER
GRADE & PURITY BioReagent ? BioReagent grade — tested suitable for life-science and molecular-biology use. Use for cell culture, assays, and biochemical work needing biological compatibility. Biological Stain ? Biological stain grade — dyes characterized for staining cells and tissues. Use in histology and microscopy where staining consistency matters. for Microscopy ? Microscopy grade — reagents/stains suited to sample prep and imaging. Use in microscopy where clarity and low background are needed. 0.1%
Synonyms
Nuclear Fast Red | Kernechtrot | Calcium Red
Storage
Protected from light,Room temperature
Shipped In
Normal
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Size
Status
Price
Qty
100ml
N743376-100ml
1
$29.90
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Why this grade

BioReagent, Biological Stain, for microscopy, 0.1% Biological Stain,BioReagent,for Microscopy for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Protected from light,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Nuclear Fast Red | Kernechtrot | Calcium Red
Specifications & Purity
BioReagent, Biological Stain, for microscopy, 0.1%
Stability And Storage
Store at room temperature long term (12 months). Store in the dark.
Storage
Protected from light, Room temperature
Shipped In
Normal
Grade
Biological Stain, BioReagent, for Microscopy
Names and Identifiers
Canonical SmilesC1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C(=C3N)O)S(=O)(=O)[O-])O.[Na+]
IUPAC Namesodium;4-amino-1,3-dihydroxy-9,10-dioxoanthracene-2-sulfonate
InChIKeyIFSXZLJQEKGQAF-UHFFFAOYSA-M
INCHI1S/C14H9NO7S.Na/c15-9-7-8(12(18)14(13(9)19)23(20,21)22)11(17)6-4-2-1-3-5(6)10(7)16;/h1-4,18-19H,15H2,(H,20,21,22);/q;+1/p-1
Isomeric SMILES C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C(=C3N)O)S(=O)(=O)[O-])O.[Na+]
WGK Germany 1
Molecular Weight 357.28
Reaxy-Rn 20093893
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20093893&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassAnthracenes
SubclassAnthraquinones
Intermediate Tree Nodes Not available
Direct ParentHydroxyanthraquinones
Alternative Parents Arylsulfonic acids and derivatives  Aryl ketones  Vinylogous amides  Vinylogous acids  Sulfonyls  Organosulfonic acids  Primary amines  Organopnictogen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Hydroxyanthraquinone - Arylsulfonic acid or derivatives - Aryl ketone - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Vinylogous amide - Vinylogous acid - Ketone - Organic alkali metal salt - Organic sodium salt - Amine - Hydrocarbon derivative - Organic oxide - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organic salt - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydroxyanthraquinones. These are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

1 results found

Lot NumberCertificate TypeDateItem
ZJ25F0420590Certificate of AnalysisFeb 10, 2026 N743376
Chemical and Physical Properties
Sensitivitylight-sensitive
Melt Point(°C)300°C
Molecular Weight357.270 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count8
Rotatable Bond Count1
Exact Mass356.992 Da
Monoisotopic Mass356.992 Da
Topological Polar Surface Area166.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity634.000
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 Count2
Documents & Articles
Biological Stain
Principles and Methodological Framework for Nucleic Acid Staining and Organelle Labeling
Quick Reference Guide to “Red” Reagents in Biological Experiments: Classification, Uses, Key Risks, and Selection Logic
Applications and Comparison of Histological Counterstaining, Collagen Evaluation, and Protein Staining Methods
Application Differences Among Highman, Bennhold, Puchtler, and Modified Methods in Congo Red Staining for Amyloid
Application Differences Among Safranin O, Alcian Blue, and Toluidine Blue in Cartilage Matrix Staining
Types, Binding Mechanisms, and Experimental Selection of Nuclear Dyes
Principles, Method Types, and Application Selection of Common Trichrome Staining Systems
Citations of This Product
References
1. Hongxia Xiu, Yajie Liu, Huihui Yang, Haibin Ren, Bowen Luo, Zhipeng Wang, Hong Shao, Fengzhong Wang, Jingjian Zhang, Yutang Wang.  (2022)  Identification of novel umami molecules via QSAR models and molecular docking.  Food & Function,  13  (14): (7529-7539).  [PMID:35765918] [10.1039/D2FO00544A]
2. Hui-Hui Xiao, Quan-Gui Gao, Ming-Xian Ho, Yan Zhang, Ka-Chun Wong, Yi Dai, Xin-Sheng Yao, Man-Sau Wong.  (2015)  An 8-O-4′ norlignan exerts oestrogen-like actions in osteoblastic cells via rapid nongenomic ER signaling pathway.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:25978953] [10.1016/j.jep.2015.05.012]
3. Junling An, Hao Li, Wenjing Wen, Gaojian Liu, Zixuan Huang, Xinwei Zhao, Gaofeng Liang.  (2025)  Dual Inhibition of GPX4 and LCN2 via miR-214-3p Loaded Iron Oxide Nanoparticles for Enhancing Ferroptosis in Liver Cancer.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.137049]
Solution Calculators
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Customer Reviews

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