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3,3'-Dimethoxybenzidine - 97%, high purity , CAS No.119-90-4

77 Citations COA COA
    Grade & Purity:
  • ≥97%
In stock
Item Number
D104001
Grouped product items
SKU Size
Availability
 Price Qty
D104001-1g
1g
3
$19.90
D104001-5g
5g
5
$25.90
D104001-25g
25g
3
$45.90
D104001-100g
100g
1
$164.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Imide (271) Peroxidase substrate (27) Polymer / polymer reagent (675)

Basic Description

Synonyms DSS | 3,3'-Dimethoxybenzidin [Czech] | Benzidine,3'-dimethoxy- | Cibacete Diazo Navy Blue 2B | Diacelliton fast grey G | Diacel Navy DC | Setacyl Diazo Navy R | Azogene Fast Blue B Salt | Cellitazol bn | DIMETHOXYBENZIDINE, 3,3'- | Hiltosal Fast Blue B Sa
Specifications & Purity ≥97%
Storage Temp Protected from light,Argon charged
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class 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
Description 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

Associated Targets(Human)

AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TNF Tclin TNF-alpha (1897 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
clpP ATP-dependent Clp protease proteolytic subunit (245 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504751669
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504751669
IUPAC Name 4-(4-amino-3-methoxyphenyl)-2-methoxyaniline
INCHI 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
InChIKey JRBJSXQPQWSCCF-UHFFFAOYSA-N
Smiles COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N)OC)N
Isomeric SMILES COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N)OC)N
UN Number 2811
Packing Group I
Molecular Weight 244.29
Reaxy-Rn 1879884
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1879884&ln=

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.

19 results found

Lot Number Certificate Type Date Item
I2308040 Certificate of Analysis Jun 09, 2025 D104001
B2512042 Certificate of Analysis Apr 14, 2025 D104001
G2503021 Certificate of Analysis Feb 17, 2025 D104001
B2512044 Certificate of Analysis Feb 17, 2025 D104001
F2505030 Certificate of Analysis Feb 17, 2025 D104001
K2401068 Certificate of Analysis Nov 09, 2024 D104001
I2403069 Certificate of Analysis Sep 11, 2024 D104001
I2216167 Certificate of Analysis Jun 14, 2024 D104001
I2216168 Certificate of Analysis Jun 14, 2024 D104001
I2216169 Certificate of Analysis Jun 14, 2024 D104001
G2426528 Certificate of Analysis Apr 25, 2024 D104001
K2419511 Certificate of Analysis Apr 25, 2024 D104001
H2124123 Certificate of Analysis May 12, 2023 D104001
H2124132 Certificate of Analysis May 12, 2023 D104001
I2216058 Certificate of Analysis Jul 06, 2022 D104001
C2405075 Certificate of Analysis Jul 06, 2022 D104001
F2201101 Certificate of Analysis Mar 23, 2022 D104001
F2201102 Certificate of Analysis Mar 23, 2022 D104001
F2201108 Certificate of Analysis Mar 23, 2022 D104001

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Chemical and Physical Properties

Solubility Soluble in alcohol, benzene, ether, chloroform, acetone, most organic solvents and lipids. Slightly soluble in water.
Sensitivity Light sensitive.Air sensitive
Flash Point(°C) 206°C
Melt Point(°C) 136-140°C
Molecular Weight 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 Ų
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

Solution Calculators

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