Reactive Yellow 86 , CAS No.61951-86-8

CAS: 61951-86-8 Cat. No.: R671382 Peso molecular: 667.37
Disponible para pedir
Synonyms
5-[[5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,4-disulfophenyl]diazenyl]-1-ethyl-4-methyl-2-oxido-6-oxopyridine-3-carboximidate | CID 101531203
Storage
Room temperature,Desiccated,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
R671382-1g
1
39,90US$
5g
R671382-5g
1
139,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated,Cool Ships Normal Check lot-specific COA for exact specifications.

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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

Reactive Yellow 86 is a synthetic dye that belongs to the class of reactive dyes. Reactive dyes are widely used in the textile industry to color natural and synthetic fibers such as cotton, wool, silk, and polyester. These dyes are known for their high colorfastness and ability to form covalent bonds with the fiber, resulting in a durable and long-lasting color. Reactive Yellow 86, also known by its chemical name C.I. Reactive Yellow 86 or by its trade names, is specifically a yellow dye within the reactive dye range. It is commonly used for dyeing textiles, including garments, fabrics, and home textiles.

Specifications

Sinónimos
5-[[5-[(4, 6-dichloro-1, 3, 5-triazin-2-yl)amino]-2, 4-disulfophenyl]diazenyl]-1-ethyl-4-methyl-2-oxido-6-oxopyridine-3-carboximidate | CID 101531203
Condiciones de almacenamiento de almacenamiento
Room temperature, Desiccated, Cool
Enviado en
Normal
Nombres e identificadores
Sonrisas canónicasCCN1C(=C(C(=C(C1=O)N=NC2=C(C=C(C(=C2)NC3=NC(=NC(=N3)Cl)Cl)S(=O)(=O)O)S(=O)(=O)O)C)C(=N)[O-])[O-].[Na+].[Na+]
IUPAC Namedisodium;5-[[5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-2,4-disulfophenyl]diazenyl]-1-ethyl-4-methyl-2-oxido-6-oxopyridine-3-carboximidate
InChIKeyWOFHPDGARHNFJI-UHFFFAOYSA-L
INCHI1S/C18H16Cl2N8O9S2.2Na/c1-3-28-14(30)11(13(21)29)6(2)12(15(28)31)27-26-8-4-7(22-18-24-16(19)23-17(20)25-18)9(38(32,33)34)5-10(8)39(35,36)37;;/h4-5,30H,3H2,1-2H3,(H2,21,29)(H,32,33,34)(H,35,36,37)(H,22,23,24,25);;/q;2*+1/p-2
Isómeros SMILES CCN1C(=C(C(=C(C1=O)N=NC2=C(C=C(C(=C2)NC3=NC(=NC(=N3)Cl)Cl)S(=O)(=O)O)S(=O)(=O)O)C)C(=N)[O-])[O-].[Na+].[Na+]
CAS alternativo 70865-29-1
Peso molecular 667.37

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
ClaseBenzene and substituted derivatives
SubclassBenzenesulfonic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonic acids and derivatives
Alternative Parents 1-sulfo,2-unsubstituted aromatic compounds  Benzenesulfonyl compounds  Nicotinamides  Aniline and substituted anilines  Pyridinones  Pyridinolates  Aminotriazines  Chloro-s-triazines  Dihydropyridines  Methylpyridines  Aryl chlorides  Sulfonyls  Organosulfonic acids  Heteroaromatic compounds  Azo compounds  Lactams  Organic metal halides  Carboximidic acids  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Organic oxides  Organic sodium salts  Organochlorides  Organooxygen compounds  Amines  Hydrocarbon derivatives  Organic cations  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Benzenesulfonate - 1-sulfo,2-unsubstituted aromatic compound - Nicotinamide - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Aniline or substituted anilines - Pyridinolate - Amino-1,3,5-triazine - Pyridinone - Chloro-s-triazine - Halo-s-triazine - Dihydropyridine - Methylpyridine - Aminotriazine - Hydropyridine - Pyridine - Triazine - 1,3,5-triazine - Aryl chloride - Aryl halide - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Azo compound - Lactam - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic metal halide - Organoheterocyclic compound - Carboximidic acid - Carboximidic acid derivative - Azacycle - Organic alkali metal salt - Organic oxygen compound - Organic salt - Organohalogen compound - Organochloride - Organonitrogen compound - Amine - Organooxygen compound - Organosulfur compound - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic cation - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzenesulfonic acids and derivatives. These are organic compounds containing a sulfonic acid or a derivative thereof that is linked 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.

5 results found

Lot NumberCertificate TypeFechaArticulo
K2405653Certificate of AnalysisOct 25, 2024 R671382
K2405654Certificate of AnalysisOct 25, 2024 R671382
K2405655Certificate of AnalysisOct 25, 2024 R671382
K2405656Certificate of AnalysisOct 25, 2024 R671382
H2405004Certificate of AnalysisJul 30, 2024 R671382
Citations of This Product
Referencias
1. Najmeh Zare, Tao Wu, Dongxing Zhang, Nianbing Zhong, Li Fu, Tejraj M. Aminabhavi, Hassan Karimi-Maleh.  (2025)  Efficient removal of Congo red using adsorbents prepared via MOF-on-MOF strategy.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.171592]
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