Fucsina de base - Corante biológico , CAS No.569-61-9

Name: Fucsina de base - Corante biológico , CAS No.569-61-9
Brand: Aladdin Scientific
SKU: B108734
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CAS: 569-61-9 Cat. No.: B108734 Fórmula: C₁₉H₁₇N₃ · HCl Peso molecular: 323.82 Beilstein Registry Number: 4164603 Número CE: 209-321-2 PubChem CID: 11292

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Fucsina de base - Corante biológico CAS No(569-61-9) by Aladdin Scientific

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GRAU & PUREZA Biological Stain ?

Synonyms

Pararosaniline hydrochloride|Pararosaniline chloride|Basic Red 9|Parafuchsin

Storage

Protegido da luz,Dessecado

Shipped In

Normal

Folha de especificações

Visão geral Especificações Nomes e identificadores Dados avançados Taxonomic Classification Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas FAQs e artigos Citations of This Product Calculadoras de soluções Revisões

Visão geral

A pararosanilina é um corante catiónico de triarilmetano e um dos componentes da fucsina básica.[1] Dá uma cor vermelha brilhante após o tingimento de fibras de poliacrilonitrilo.

Aplicações：

O cloridrato de pararosanilina tem sido usado: para preparar o reagente de Schiff ； para corar amostras de citologia endometrial de vaca ； para contracoloração de seções de azul da Prússia de cérebros de camundongos.

Especificações

Sinónimos

Pararosaniline hydrochloride | Pararosaniline chloride | Basic Red 9 | Parafuchsin

Especificações e pureza

Corante biológico

Condições de armazenamento de armazenamento

Protegido da luz,Dessecado

Enviado em

Normal

Grau

Biological Stain

Nomes e identificadores

Pubchem Sid

508815036

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508815036

Sorrisos canónicos

Cl.Nc1ccc(cc1)C(\c2ccc(N)cc2)=C3/C=CC(=N)C=C3

IUPAC Name

4-[(4-aminophenyl)-(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydrochloride

InChIKey

JUQPZRLQQYSMEQ-UHFFFAOYSA-N

INCHI

1S/C19H17N3.ClH/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15;/h1-12,20H,21-22H2;1H

SMILES isoméricas

C1=CC(=N)C=CC1=C(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N.Cl

WGK Alemanha

RTECS

CX9850100

PubChem CID

11292

Peso molecular

323.82

Beilstein

4164603

Reaxy-Rn

4164603

Dados avançados

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Classe Benzene and substituted derivatives
    - Subclass Diphenylmethanes

Kingdom	Organic compounds
Superclass	Benzenoids
Classe	Benzene and substituted derivatives
Subclass	Diphenylmethanes
Intermediate Tree Nodes	Not available
Direct Parent	Diphenylmethanes
Alternative Parents	Aniline and substituted anilines Ketimines Primary amines Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Diphenylmethane - Aniline or substituted anilines - Ketimine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Imine - Carbonyl group - Amine - Aromatic homomonocyclic compound
Descrição	This 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	hydrochloride
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Estrutura 3D

Alvos associados (humanos)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TNF Tclin TNF-alpha (1897 Activities)

Discover Target: TNF

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CXCL8 Tchem Interleukin-8 (642 Activities)

Discover Target: CXCL8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)

Discover Target: GBA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)

Discover Target: ALOX15B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)

Discover Target: NFKB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Data	Item
D2607164	Certificate of Analysis	Mar 20, 2026	B108734
D2607165	Certificate of Analysis	Mar 20, 2026	B108734
B2624032	Certificate of Analysis	Jan 24, 2026	B108734
B2624033	Certificate of Analysis	Jan 24, 2026	B108734
E2513147	Certificate of Analysis	Apr 29, 2025	B108734
E2513148	Certificate of Analysis	Apr 29, 2025	B108734
I2406100	Certificate of Analysis	Aug 27, 2024	B108734
I2406101	Certificate of Analysis	Aug 27, 2024	B108734
G2431081	Certificate of Analysis	Jul 12, 2024	B108734
G2431082	Certificate of Analysis	Jul 12, 2024	B108734
C2303462	Certificate of Analysis	Feb 10, 2023	B108734
C2303463	Certificate of Analysis	Feb 10, 2023	B108734
C2303465	Certificate of Analysis	Feb 10, 2023	B108734
C2303466	Certificate of Analysis	Feb 10, 2023	B108734

Sensibilidade	light sensitive
Ponto de fusão (°C)	270℃
Peso molecular	323.800 g/mol
XLogP3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	2
Exact Mass	323.119 Da
Monoisotopic Mass	323.119 Da
Topological Polar Surface Area	75.900 Å²
Heavy Atom Count	23
Formal Charge	0
Complexity	457.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

Fucsina de base - Corante biológico , CAS No.569-61-9

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