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

CAS: 467-62-9 Cat. No.: P106803 Summenformel: C₁₉H₁₉N₃O Molekulargewicht: 305.37 Beilstein Registry Number: 2148632 EG-Nummer: 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

Übersicht

Product Application:

diagnostic assay manufacturing；hematology；histology

Specifications

Synonyme

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

Spezifikationen & Reinheit

≥95%

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥95%

Namen und Kennungen

• Pubchem Sid: 488181079
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181079
• Kanonisches Lächeln: 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
• Isomere SMILES: C1=CC(=CC=C1C(C2=CC=C(C=C2)N)(C3=CC=C(C=C3)N)O)N
• WGK Deutschland: 3
• Molekulargewicht: 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
    • Klasse Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: 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
• Beschreibung: 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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: ethanol: 1 mg/mL, clear to hazy
• Schmelzpunkt (°C): 205°C
• Molekulargewicht: 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

Referenzen

1. Yu-Gang Fu, Han-Qiao Liu, Cong Liu, Qiu-Feng Lü.  (2023)  Ultralight porous carbon loaded Co-doped MoS2 as an efficient electrocatalyst for hydrogen evolution reaction in acidic and alkaline media.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2023.171748]

2. Yiran Dou, Cong Liu, Xiaocui Chen, Xiumin Yang, Lin Hao, Qianqian Wang, Zhi Wang, Qiuhua Wu, Chun Wang.  (2024)  Green synthesis of azo-linked porous organic polymer for enrichment of nitroimidazoles from water, shrimp and Basa fish.  FOOD CHEMISTRY,      [PMID:38430772] [10.1016/j.foodchem.2024.138875]

3. Yuqi Zhuang, Sinuo Li, Eldon R. Rene, Shuoyu Dong, Weifang Ma.  (2024)  Green synthesis of magnetic azo-linked porous organic polymers with recyclable properties for enhanced Bisphenol-A adsorption from aqueous solutions.  ENVIRONMENTAL RESEARCH,      [PMID:38325780] [10.1016/j.envres.2024.118427]