Pararosaniline Base - ≥95% , CAS No.467-62-9

CAS: 467-62-9 Cat. No.: P106803 Formule: C₁₉H₁₉N₃O Poids moléculaire: 305.37 Beilstein Registry Number: 2148632 Numéro CE: 207-395-0

GRADE & PURITY ≥95%

Synonyms

4,4',4''-Triaminotrityl alcohol | BENZENAMINE,4-[(4-AMINOPHENYL)(4-IMINO-2,5-CYCLOHEXADIEN-1-YLIDENE)METHYL]-, CONJUGATE ACID(1:1) | Ci42500 | tris-(4-aminophenyl)methanol | Tris(4-aminophenyl)methanol | 4,4',4''-Triaminotriphenylcarbinol | Fuchsin dye ba

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

Product Application:

diagnostic assay manufacturing；hematology；histology

Specifications

Synonymes

4,4',4''-Triaminotrityl alcohol | BENZENAMINE,4-[(4-AMINOPHENYL)(4-IMINO-2,5-CYCLOHEXADIEN-1-YLIDENE)METHYL]-, CONJUGATE ACID(1:1) | Ci42500 | tris-(4-aminophenyl)methanol | Tris(4-aminophenyl)methanol | 4,4',4''-Triaminotriphenylcarbinol | Fuchsin dye ba

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥95%

Noms et identifiants

• Pubchem Sid: 488181079
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181079
• Sourires canoniques: C1=CC(=CC=C1C(C2=CC=C(C=C2)N)(C3=CC=C(C=C3)N)O)N
• IUPAC Name: tris(4-aminophenyl)methanol
• InChIKey: KRVRUAYUNOQMOV-UHFFFAOYSA-N
• INCHI: 1S/C19H19N3O/c20-16-7-1-13(2-8-16)19(23,14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15/h1-12,23H,20-22H2
• Isomères SMILES: C1=CC(=CC=C1C(C2=CC=C(C=C2)N)(C3=CC=C(C=C3)N)O)N
• WGK Allemagne: 3
• Poids moléculaire: 305.37
• Beilstein: 2148632
• Reaxy-Rn: 2148632
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2148632&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Triphenyl compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Triphenyl compounds
• Alternative Parents: Aniline and substituted anilines Tertiary alcohols Primary amines Organopnictogen compounds Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenyl compound - Aniline or substituted anilines - Monocyclic benzene moiety - Tertiary alcohol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic alcohol - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.
• External Descriptors: Not available

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

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: ethanol: 1 mg/mL, clear to hazy
• Point de fusion (°C): 205°C
• Poids moléculaire: 305.400 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 305.153 Da
• Monoisotopic Mass: 305.153 Da
• Topological Polar Surface Area: 98.300 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 310.000
• 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