Name: 3,3'-Dimethoxybenzidine - analytical standard , CAS No.119-90-4
Brand: Aladdin Scientific
SKU: D104002
Availability: InStock

3,3'-Dimethoxybenzidine - analytical standard , CAS No.119-90-4

CAS: 119-90-4 Cat. No.: D104002 Fórmula: C₁₄H₁₆N₂O₂ Peso molecular: 244.29 Número EC: 204-355-4

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3,3'-Dimethoxybenzidine - analytical standard CAS No(119-90-4) by Aladdin Scientific

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Synonyms

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Especificaciones Nombres e identificadores Datos avanzados Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Preguntas frecuentes y artículos Citations of This Product Calculadoras de soluciones Reseñas

Especificaciones

Sinónimos

Especificaciones y pureza

analytical standard

Condiciones de almacenamiento de almacenamiento

Protected from light,Room temperature

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Grado

Patrón analítico

Nombres e identificadores

Pubchem Sid

528757800

Sonrisas canónicas

COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N)OC)N

IUPAC Name

4-(4-amino-3-methoxyphenyl)-2-methoxyaniline

InChIKey

JRBJSXQPQWSCCF-UHFFFAOYSA-N

INCHI

1S/C14H16N2O2/c1-17-13-7-9(3-5-11(13)15)10-4-6-12(16)14(8-10)18-2/h3-8H,15-16H2,1-2H3

Isómeros SMILES

COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N)OC)N

Número ONU

2811

Grupo de embalaje

Peso molecular

244.29

Reaxy-Rn

1879884

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1879884&ln=

Datos avanzados

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Clase Benzene and substituted derivatives
    - Subclass Biphenyls and derivatives
      - Level5 Benzidines
        Level6 3,3'-disubstituted benzidines

Kingdom	Organic compounds
Superclass	Benzenoids
Clase	Benzene and substituted derivatives
Subclass	Biphenyls and derivatives
Intermediate Tree Nodes	Benzidines
Direct Parent	3,3'-disubstituted benzidines
Alternative Parents	Methoxyanilines Aminophenyl ethers Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers Primary amines Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	3,3'-disubstituted benzidine - Aminophenyl ether - Methoxyaniline - Phenoxy compound - Anisole - Phenol ether - Aniline or substituted anilines - Methoxybenzene - Alkyl aryl ether - Ether - Primary amine - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Aromatic homomonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as 3,3'-disubstituted benzidines. These are organic compounds containing a benzidine skeleton, which is substituted only at the 3- and 3'-positions.
External Descriptors	a small molecule
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

Estructura 3D

Objetivos asociados (humanos)

AR Tclin Androgen Receptor (11781 Activities)

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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

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TNF Tclin TNF-alpha (1897 Activities)

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

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

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GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

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KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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GMNN Tbio Geminin (128009 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

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ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)

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BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)

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Objetivos asociados (no humanos)

Plasmodium falciparum (966862 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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Impa1 Inositol monophosphatase 1 (16203 Activities)

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clpP ATP-dependent Clp protease proteolytic subunit (245 Activities)

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Mecanismos de acción

Certificados (CoA, COO, BSE/TSE y tabla de análisis)

C of A & Other Certificates(BSE/TSE, COO):

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Lot Number	Certificate Type	Fecha	Articulo
G2101107	Certificate of Analysis	Oct 09, 2026	D104002

Propiedades químicas y físicas

Sensibilidad	Light sensitive.
Punto de inflamación (°C)	206°C
Punto de fusión (°C)	136-140°C
Peso molecular	244.290 g/mol
XLogP3	2.200
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	3
Exact Mass	244.121 Da
Monoisotopic Mass	244.121 Da
Topological Polar Surface Area	70.500 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	236.000
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	1

Preguntas frecuentes y artículos

Famotidine: Physicochemical Features, Mechanism of Action, and Key Points for Research Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Pepsin cAMP PK/PD famotidine H2-receptor antagonist gastric acid secretion pH-dependent absorption renal excretion histamine signaling

Citations of This Product

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Reseñas

📚 Citas por aplicación

Extraction & workup solvent15

Organic synthesis — reaction medium22

Other applications56

Drug / compound screening13

Topical & ophthalmic formulation2

Controlled-release & nanoparticle carrier11

Chromatography (HPLC / GC / TLC)6

Cell proliferation2

Cytotoxicity screening8

Nanoparticle / material biocompatibility2

Electrochemistry & battery electrolyte2

Cell viability4

Polymer synthesis & polymerization1

Spectroscopy sample preparation3

Cancer cell line characterization2

Crystallization & recrystallization1

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