1,1,3,3,5,5,7,7,9,9,11,11,13,13-Tetradecamethylheptasiloxane - ≥95% , CAS No.19095-23-9

CAS: 19095-23-9 Cat. No.: T405046 Peso molecular: 505.1 PubChem CID: 6329088

GRADE & PURITY ≥95%

Synonyms

1,1,3,3,5,5,7,7,9,9,11,11,13,13-Tetradecamethylheptasiloxane | T3548 | MFCD30721597 | SCHEMBL9004474 | 1,1,3,3,5,5,7,7,9,9,11,11,13,13-Tetradecamethylheptasiloxane # | 1,1,3,3,5,5,7,7,9,9,11,11,13,13-tetradecamethyl-h eptasiloxane | Heptasiloxane, 1,1,3,3

Storage

Argon charged,Room temperature

Specifications

Sinónimos

1, 1, 3, 3, 5, 5, 7, 7, 9, 9, 11, 11, 13, 13-Tetradecamethylheptasiloxane | T3548 | MFCD30721597 | SCHEMBL9004474 | 1, 1, 3, 3, 5, 5, 7, 7, 9, 9, 11, 11, 13, 13-Tetradecamethylheptasiloxane # | 1, 1, 3, 3, 5, 5, 7, 7, 9, 9, 11, 11, 13, 13-tetradecamethyl-h eptasiloxane | Heptasiloxane, 1, 1, 3, 3

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 488195708
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488195708
• Sonrisas canónicas: C[Si](C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)C
• InChIKey: JJIDUNHDYJESJA-UHFFFAOYSA-N
• INCHI: 1S/C14H42O6Si7/c1-21(2)15-23(5,6)17-25(9,10)19-27(13,14)20-26(11,12)18-24(7,8)16-22(3)4/h1-14H3
• Isómeros SMILES: C[Si](C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)C
• PubChem CID: 6329088
• Peso molecular: 505.1
• Reaxy-Rn: 2003651

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Siloxanes
• Alternative Parents: Organoheterosilanes Organic metalloid salts Organic oxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Siloxane - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as siloxanes. These are saturated silicon-oxygen hydrides with unbranched or branched chains of alternating silicon and oxygen atoms (each silicon atom is separated from its nearest silicon neighbours by single oxygen atoms). The general structure of unbranched siloxanes is H3Si[OSiH2]nOSiH3. H3Si[OSiH2]nOSiH[OSiH2OSiH3]2 is an example of a branched siloxane. By extension hydrocarbyl derivatives are commonly included.
• 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

Propiedades químicas y físicas

• Sensibilidad: Air Sensitive
• Índice de refracción: 1.39
• Punto de inflamación (°C): 164 °C
• Punto de ebullición (°C): 128 °C/2 mmHg
• Peso molecular: 503.070 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 12
• Exact Mass: 502.137 Da
• Monoisotopic Mass: 502.137 Da
• Topological Polar Surface Area: 55.400 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 429.000
• 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

XLogP3

Referencias

1. Guangming Lu, Shu Tian, Jingyu Li, Yongjian Xu, Shuan Liu, Jibin Pu.  (2020)  Fabrication of bio-based amphiphilic hydrogel coating with excellent antifouling and mechanical properties.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2020.128134]