4,4'-Diaminodiphenyl Sulfone（DDS） - Moligand™, ≥99.5%, used for Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O

CAS: 80-08-0 Cat. No.: D1507143 Formule: C₁₂H₁₂N₂O₂S Poids moléculaire: 248.3 Beilstein Registry Number: 788055 Numéro CE: 201-248-4

QUALITÉ & PURETÉ Moligand™, ≥99.5%

Synonyms

Bis(4-aminophenyl) sulfone | 4-Aminophenyl sulfone | 4,4'-Sulfonyldianiline | 4,4'-Diaminodiphenyl Sulfone

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Vue d’ensemble

4-Aminobenzenesulfone (DDS) is a diamine curing agent used for curing epoxy resins.

Product application:

Product application: Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O3), forming flame-retardant epoxy resin nanocomposites. It can also be used as a curing agent to cure bisphenol A (DGEBA) used in the manufacture of flame-retardant epoxy resin/clay nanocomposites.

Spécifications

Synonymes

Bis(4-aminophenyl) sulfone | 4-Aminophenyl sulfone | 4,4'-Sulfonyldianiline | 4,4'-Diaminodiphenyl Sulfone

Spécifications et pureté

Moligand™, ≥99.5%

Application

Tetrafunctional epoxy resin can be mixed with DDS and can be heat cured for oilfield applications. DDS can also be used to cure layered double hydroxide based epoxy resins of iron oxide (Fe2O3), forming flame-retardant epoxy resin nanocomposites. It can a

Conditions de stockage de stockage

Store at 2-8°C,Protected from light

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Pureté

≥99.5%

Propriétés du produit

ALogP

1

Noms et identifiants

Sourires canoniques

NC1=CC=C(C=C1)S(=O)(=O)C1=CC=C(N)C=C1

IUPAC Name

4,4'-Sulfonyldianiline

InChIKey

MQJKPEGWNLWLTK-UHFFFAOYSA-N

INCHI

InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2

Isomères SMILES

C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N

WGK Allemagne

1

RTECS

BY8925000

Poids moléculaire

248.3

Beilstein

788055

Reaxy-Rn

788055

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=788055&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzenesulfonyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzenesulfonyl compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzenesulfonyl compounds
• Alternative Parents: Aniline and substituted anilines Sulfones Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzenesulfonyl group - Aniline or substituted anilines - Sulfonyl - Sulfone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzenesulfonyl compounds. These are aromatic compounds containing a benzenesulfonyl group, which consists of a monocyclic benzene moiety that carries a sulfonyl group.
• External Descriptors: sulfone - substituted aniline

Data sources

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

Propriétés chimiques et physiques

• Solubilité: Insoluble in water. Solubility in hot methanol is almost transparent. Soluble in DMSO, ethanol and acetone.
• Sensibilité: Moisture sensitive；Light sensitive
• Point de fusion (°C): 173-178°C