Basic Fuchsin indicator - 0.1% , CAS No.632-99-5

CAS: 632-99-5 Cat. No.: B299251 Fórmula: C20H20ClN3 Peso molecular: 337.85 Número EC: 211-189-6
Disponible para pedir
CALIDAD & PUREZA 0.1%
Synonyms
Fuchsin, basic | MAGENTA | Benzenamine, 4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2-methyl-, monohydrochloride | Basic fuchsin, indicator | Fuchsine RTN | AI3-18324 | BASIC VIOLET 14 [INCI] | CI Basic Violet 14, monohydrochloride | Ma
Storage
Room temperature
Shipped In
Normal
★
Talla
Alemania (EU)
USA*
Precio
Cantidad
100ml
B299251-100ml
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Por qué esta calidad

0.1% para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

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Almacenamiento y envío

Room temperature Envío Normal. Consulte el COA específico del lote para conocer las especificaciones exactas.

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Documentos de calidad

SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.

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Prueba documental

Citado en 24 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Descripción general

Basic Fuchsin is a dye composed of rosaniline, magenta II, pararosaniline, and new fuschsine. The fluorescent dye has been used for Ziehl-Neelson staining in order to detect acid-fast bacilli. The dyes fluorescence has been useful in understanding microfissures, as it allows a clear delineation of surface level structure and constant background from the microscope. Basic Fuchsin staining includes tissue sections to visualize elastic fibers, and cardiac and skeletal muscle tissue. Reports show that Basic Fuchsin has the ability to stain tubercle Bacillus, bacterial flagella, and to compare Escherichia coli and Aerobacter aerogenes.

Especificaciones

Sinónimos
Fuchsin, basic | MAGENTA | Benzenamine, 4-((4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl)-2-methyl-, monohydrochloride | Basic fuchsin, indicator | Fuchsine RTN | AI3-18324 | BASIC VIOLET 14 [INCI] | CI Basic Violet 14, monohydrochloride | Ma
Especificaciones y pureza
0.1%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
CC1=CC(=C(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N)C=CC1=N.Cl
IUPAC Name
4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydrochloride
InChIKey
AXDJCCTWPBKUKL-UHFFFAOYSA-N
INCHI
1S/C20H19N3.ClH/c1-13-12-16(6-11-19(13)23)20(14-2-7-17(21)8-3-14)15-4-9-18(22)10-5-15;/h2-12,23H,21-22H2,1H3;1H
Isómeros SMILES
CC1=CC(=C(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N)C=CC1=N.Cl
Peso molecular
337.85
Reaxy-Rn
4039689
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4039689&ln=

Documentación

📋 Hoja de datos de seguridad (SDS)

Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.

<<<<<<< HEAD Descargar SDS → ======= Descargar SDS → >>>>>>> release248-p3

✅ Certificado de análisis (COA)

Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.

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📊 Ficha técnica

Resumen de referencia rápida de las especificaciones y aplicaciones del producto.

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🔬 Hoja de especificaciones

Atributos de calidad completos y criterios de aceptación para esta calidad.

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Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassDiphenylmethanes
Intermediate Tree Nodes Not available
Direct ParentDiphenylmethanes
Alternative Parents Monocyclic monoterpenoids  Aromatic monoterpenoids  Aniline and substituted anilines  Ketimines  Primary amines  Organopnictogen compounds  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Diphenylmethane - Aromatic monoterpenoid - Monocyclic monoterpenoid - Monoterpenoid - Aniline or substituted anilines - Ketimine - Hydrochloride - Primary amine - Organonitrogen compound - Amine - Imine - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organopnictogen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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2 results found

Lot NumberCertificate TypeFechaArticulo
B2225401B2225401Certificate of AnalysisJan 19, 2026 B299251
L2007245L2007245Certificate of AnalysisSep 21, 2024 B299251
Propiedades químicas y físicas
SolubilidadSoluble in alcohol, water (4 g/l) at 25 °C, and acids practic. Insoluble in ether.
Peso molecular337.800 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass337.135 Da
Monoisotopic Mass337.135 Da
Topological Polar Surface Area75.900 Ų
Heavy Atom Count24
Formal Charge0
Complexity515.000
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
Preguntas frecuentes y artículos
PAS Staining (Periodic Acid–Schiff, PAS) Standard Operating Procedure (SOP)
Quick Reference Guide to “Red” Reagents in Biological Experiments: Classification, Uses, Key Risks, and Selection Logic
Glutaraldehyde-mediated Microbial Inactivation: Chemical Mechanisms, Determinants, and Key Validation Considerations
Applications and Differences of Neisser Staining, Albert Staining, and Gram Staining in the Differentiation of Corynebacteria
Microbial Morphological Identification: Observation Systems, Staining Methods, and Result Interpretation
Structural Characteristics, Color-Change Mechanisms, and Application Selection of Triphenylmethane Dye-Type Indicators
Elastic Fiber Staining Methods: Comparison of Orcein, Verhoeff, Weigert, and Victoria Blue Methods
Histological Staining Methods for Identifying Hepatitis B Virus: Comparison of HE, Orcein, Aldehyde Fuchsin, Victoria Blue, Immunohistochemistry, and In Situ Hybridization
Analysis of Classical Histological Special Staining Systems: Application Selection of PTAH, Masson, VG, Elastic Fiber Staining, and Reticular Fiber Staining
Summary of Cell Staining Methods
Citations of This Product
Calculadoras de soluciones
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