Mordant Yellow 10 - ≥80% , CAS No.6054-99-5

CAS: 6054-99-5 Cat. No.: M137641 Peso molecular: 366.26 Número EC: 227-976-2 PubChem CID: 135465067
Disponible para pedir
GRADE & PURITY ≥80%
Synonyms
SCHEMBL428681 | Rolipram - CAS 61413-54-5 | Benzoic acid, 2-hydroxy-5-[(4-sulfophenyl)azo]-, disodium salt | MFCD00007504 | 2-hydroxy-5-((4-sulfophenyl)azo)benzoic acid | Acid Chrome Yellow | Chrome Yellow 2J | Eniacromo Yellow GR | Durochrome Yellow 2G |
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
M137641-1g
5
9,90US$
5g
M137641-5g
5
9,90US$
25g
M137641-25g
5
25,90US$
100g
M137641-100g
8
52,90US$
500g
M137641-500g
1
153,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥80% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Mordant Yellow 10 is a monoazo dye used in wool textiles. Mordant Yellow 10 is used as organic reagent for spectrometric determination of iron(III) as well as in the study of other metal complexations.
An organic reagent for spectrometric determination of iron (III)

Specifications

Sinónimos
SCHEMBL428681 | Rolipram - CAS 61413-54-5 | Benzoic acid, 2-hydroxy-5-[(4-sulfophenyl)azo]-, disodium salt | MFCD00007504 | 2-hydroxy-5-((4-sulfophenyl)azo)benzoic acid | Acid Chrome Yellow | Chrome Yellow 2J | Eniacromo Yellow GR | Durochrome Yellow 2G |
Especificaciones y pureza
≥80%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥80%
Nombres e identificadores
Pubchem Sid504773345
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504773345
Sonrisas canónicasC1=CC(=CC=C1N=NC2=CC(=C(C=C2)[O-])C(=O)O)S(=O)(=O)[O-].[Na+].[Na+]
IUPAC Namedisodium;4-[(3-carboxy-4-oxidophenyl)diazenyl]benzenesulfonate
InChIKeyYEVMULNVFDCUTD-UHFFFAOYSA-L
INCHI1S/C13H10N2O6S.2Na/c16-12-6-3-9(7-11(12)13(17)18)15-14-8-1-4-10(5-2-8)22(19,20)21;;/h1-7,16H,(H,17,18)(H,19,20,21);;/q;2*+1/p-2
Isómeros SMILES C1=CC(=CC=C1N=NC2=CC(=C(C=C2)[O-])C(=O)O)S(=O)(=O)[O-].[Na+].[Na+]
PubChem CID 135465067
Peso molecular 366.26

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
SuperclassOrganoheterocyclic compounds
ClaseAzobenzenes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentAzobenzenes
Alternative Parents Benzenesulfonic acids and derivatives  Benzoic acids  Benzenesulfonyl compounds  1-sulfo,2-unsubstituted aromatic compounds  Benzoyl derivatives  Phenoxides  Vinylogous acids  Sulfonyls  Organosulfonic acids  Carboxylic acid salts  Azo compounds  Propargyl-type 1,3-dipolar organic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organooxygen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Azobenzene - Benzenesulfonate - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Benzoic acid - Benzoic acid or derivatives - Arylsulfonic acid or derivatives - Benzoyl - Phenoxide - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxylic acid salt - Azo compound - Organic alkali metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as azobenzenes. These are organonitrogen aromatic compounds that contain a central azo group, where each nitrogen atom is conjugated to a benzene ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

7 results found

Lot NumberCertificate TypeFechaArticulo
C1523069Certificate of AnalysisApr 15, 2026 M137641
A2206281Certificate of AnalysisJul 09, 2025 M137641
A2206274Certificate of AnalysisJul 09, 2025 M137641
H2127556Certificate of AnalysisJun 08, 2023 M137641
H2127557Certificate of AnalysisJun 08, 2023 M137641
H2127441Certificate of AnalysisJun 08, 2023 M137641
H2127442Certificate of AnalysisJun 08, 2023 M137641
Propiedades químicas y físicas
Peso molecular366.260 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count8
Rotatable Bond Count3
Exact Mass365.99 Da
Monoisotopic Mass365.99 Da
Topological Polar Surface Area151.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity508.000
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 Count3
Citations of This Product
Referencias
1. Yanqun Zhang, Pengran Guo, Manyu Jin, Ge Gao, Qiaoyue Xi, Hua Zhou, Guobao Xu, Jingwei Xu.  (2018)  Promoting the Photo-Fenton catalytic activity with carbon dots: Broadening light absorption, higher applicable pH and better reuse performance.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2018.12.003]
Calculadoras de soluciones
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