4,4'-Dimethoxydiphenylamine - ≥98% , CAS No.101-70-2

CAS: 101-70-2 Cat. No.: D102490 Peso molecular: 229.28 Número EC: 202-968-1
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
MFCD00014895 | 4-Methoxy-N-(4-methoxyphenyl)aniline | UNII-I912MLM9XT | EINECS 202-968-1 | Oprea1_575517 | 4,4'-DIMETHOXYDIPHENYLAMINE | 4,4-DIMETHOXYDIPHENYLAMINE | Di-(4-methoxy phenyl) amine | Difenam | D0632 | AKOS003236274 | SB66814 | AM84302 | STK28
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D102490-1g
5
9,90US$
5g
D102490-5g
3
15,90US$
25g
D102490-25g
7

38,90US$

58,90US$
Guardar 20,00 US$ (33.96%)
100g
D102490-100g
1
209,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

4,4′-Dimethoxydiphenylamine is an electron donor and used in the synthesis of organic nonlinear optical (NLO) chromophores which exhibit high thermal and chemical stability, high degree of non-linearity and transparency. They are used in high performance photonic devices. They can be readily incorporated into polymers because they can be easily functionalised.
Used in the synthesis of amine electron donating groups in organic donor-bridge-acceptor dyads in Dye Sensitized Solar Cells (DSSC).

Specifications

Sinónimos
MFCD00014895 | 4-Methoxy-N-(4-methoxyphenyl)aniline | UNII-I912MLM9XT | EINECS 202-968-1 | Oprea1_575517 | 4, 4'-DIMETHOXYDIPHENYLAMINE | 4, 4-DIMETHOXYDIPHENYLAMINE | Di-(4-methoxy phenyl) amine | Difenam | D0632 | AKOS003236274 | SB66814 | AM84302 | STK28
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488180488
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180488
Sonrisas canónicasCOC1=CC=C(C=C1)NC2=CC=C(C=C2)OC
IUPAC Name4-methoxy-N-(4-methoxyphenyl)aniline
InChIKeyVCOONNWIINSFBA-UHFFFAOYSA-N
INCHI1S/C14H15NO2/c1-16-13-7-3-11(4-8-13)15-12-5-9-14(17-2)10-6-12/h3-10,15H,1-2H3
Isómeros SMILES COC1=CC=C(C=C1)NC2=CC=C(C=C2)OC
RTECS DU9085000
Peso molecular 229.28
Reaxy-Rn 2214262
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2214262&ln=

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
SuperclassBenzenoids
ClasePhenol ethers
SubclassAminophenyl ethers
Intermediate Tree Nodes Not available
Direct ParentAminophenyl ethers
Alternative Parents Methoxyanilines  Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  Secondary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aminophenyl ether - Methoxyaniline - Phenoxy compound - Anisole - Aniline or substituted anilines - Methoxybenzene - Alkyl aryl ether - Monocyclic benzene moiety - Secondary amine - Ether - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aminophenyl ethers. These are aromatic compounds that contain a phenol ether, which carries an amine group on the benzene ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GAA Tclin Lysosomal alpha-glucosidase (35701 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRCA1 Tchem Breast cancer type 1 susceptibility protein (15908 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NPC1 Tchem Niemann-Pick C1 protein (18985 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAB9A Tbio Ras-related protein Rab-9A (22488 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MBNL1 Tbio Muscleblind-like protein 1 (34431 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 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
Objetivos asociados (no humanos)
tat Human immunodeficiency virus type 1 Tat protein (75 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dnaB Replicative DNA helicase (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npsr1 Neuropeptide S receptor (260 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Large T antigen (1457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
recA Protein RecA (2211 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.

21 results found

Lot NumberCertificate TypeFechaArticulo
F2609380Certificate of AnalysisMay 27, 2026 D102490
F2609379Certificate of AnalysisMay 27, 2026 D102490
F2609336Certificate of AnalysisMay 27, 2026 D102490
F2609335Certificate of AnalysisMay 27, 2026 D102490
F2609334Certificate of AnalysisMay 27, 2026 D102490
C2429338Certificate of AnalysisMar 09, 2024 D102490
C2429335Certificate of AnalysisMar 09, 2024 D102490
C2429330Certificate of AnalysisMar 09, 2024 D102490
C2429337Certificate of AnalysisMar 09, 2024 D102490
C2429331Certificate of AnalysisMar 09, 2024 D102490
G1917023Certificate of AnalysisMay 06, 2023 D102490
E1922092Certificate of AnalysisMar 09, 2023 D102490
D2526042Certificate of AnalysisNov 23, 2022 D102490
C23311681Certificate of AnalysisNov 23, 2022 D102490
L2206440Certificate of AnalysisNov 23, 2022 D102490
L2206441Certificate of AnalysisNov 23, 2022 D102490
L2206442Certificate of AnalysisNov 23, 2022 D102490
L2206443Certificate of AnalysisNov 23, 2022 D102490
L2206444Certificate of AnalysisNov 23, 2022 D102490
L2206445Certificate of AnalysisNov 23, 2022 D102490
L2426218Certificate of AnalysisNov 23, 2022 D102490

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Propiedades químicas y físicas
SolubilidadSoluble in methanol. Insoluble in water.
SensibilidadAir sensitive;Heat sensitive
Punto de fusión (°C)100-104℃
Peso molecular229.270 g/mol
XLogP33.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass229.11 Da
Monoisotopic Mass229.11 Da
Topological Polar Surface Area30.500 Ų
Heavy Atom Count17
Formal Charge0
Complexity184.000
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 Count1
Citations of This Product
Referencias
1. Hang Yu, Dewang Li, Huayu Bao, Zhenhu Zhang, Hongli Liu, Fei Zhang, Shirong Wang.  (2022)  Multifunctional Cross-Linked Hole Transporting Interfacial Layer for Efficient and Stable Perovskite Solar Cells.  ACS Applied Energy Materials,      [PMID:] [10.1021/acsaem.2c01470]
2. Tingting Wu, Yue Liu, Jing Ye, Yi Chen, Gaole Dai, Xiaohong Zhang, Yu Zhao.  (2024)  High performance phenothiazine-based battery materials achieved by synergistic steric blocking and extended conjugation.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2024.234779]
Calculadoras de soluciones
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