Tyloxapol - 10mM in DMSO , CAS No.25301-02-4

CAS: 25301-02-4 Cat. No.: T422878 Summenformel: (C₁₅H₂₁O(C₂H₄O)m)n Molekulargewicht: 261.38 (monomer) EG-Nummer: 684-193-2

GRADE & PURITY 10mM in DMSO

Synonyms

Tyloxapol|25301-02-4|Macrocyclon|Tyloxypal|Triton WR-1339|Superinone|Alevaire|NSC90255|formaldehyde;oxirane;4-(2,4,4-trimethylpentan-2-yl)phenol|Triton A-20|Superiuone|component of Alevaire|formaldehyde; oxirane; 4-(1,1,3,3-tetramethylbutyl)phenol|SCHEMBL

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

A nonionic liquid polymer of the alkyl aryl polyether alcohol type. Used as a surfactant.

Specifications

Synonyme

Tyloxapol | 25301-02-4 | Macrocyclon | Tyloxypal | Triton WR-1339 | Superinone | Alevaire | NSC90255 | formaldehyde;oxirane;4-(2,4,4-trimethylpentan-2-yl)phenol | Triton A-20 | Superiuone | component of Alevaire | formaldehyde; oxirane; 4-(1,1,3,3-tetramethylbutyl)phenol | SCHEMBL

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

• Pubchem Sid: 528771025
• Kanonisches Lächeln: CC(C)(C)CC(C)(C)C1=CC=C(C=C1)O.C=O.C1CO1
• IUPAC Name: formaldehyde;oxirane;4-(2,4,4-trimethylpentan-2-yl)phenol
• InChIKey: MDYZKJNTKZIUSK-UHFFFAOYSA-N
• INCHI: 1S/C14H22O.C2H4O.CH2O/c1-13(2,3)10-14(4,5)11-6-8-12(15)9-7-11;1-2-3-1;1-2/h6-9,15H,10H2,1-5H3;1-2H2;1H2
• Isomere SMILES: CC(C)(C)CC(C)(C)C1=CC=C(C=C1)O.C=O.C1CO1
• WGK Deutschland: 2
• RTECS: SM9750000
• Molekulargewicht: 261.38 (monomer)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Carbonyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbonyl compounds
• Alternative Parents: Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as carbonyl compounds. These are organic compounds containing a carbonyl group, with the general structure RC(=O)R', where R=organyl, R'=H, N, O, organyl group or halide group.
• 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

Chemische und physikalische Eigenschaften

• Flammpunkt (°F): 235.4 °F
• Flammpunkt (°C): 113°C
• Molekulargewicht: 280.400 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 280.204 Da
• Monoisotopic Mass: 280.204 Da
• Topological Polar Surface Area: 49.800 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 204.000
• 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: 3

XLogP3

Referenzen

1. Qiuhe Wang, Zheng Wu, Feifei Wang, Hua Zhang, Li Gan.  (2023)  Tacrolimus-Loaded Cationic Nanoemulsion In-Situ Gel System: In-Vitro Characterization and Performance in a Dry-Eye Rabbit Model.  JOURNAL OF PHARMACEUTICAL SCIENCES,      [PMID:37453530] [10.1016/j.xphs.2023.05.001]

2. Junming Li, Xinxin Liang, Shuo Ma, Jingxin Gou, Tian Yin, Haibing He, Xing Tang, Jiansong Zhao, Yu Zhang.  (2026)  Tacrolimus cationic nanoemulsion enhances ocular surface retention for the treatment of dry eye disease and allergic conjunctivitis.  EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS,      [PMID:42520946] [10.1016/j.ejpb.2026.115199]