Triethylsilanol - ≥97% , CAS No.597-52-4

CAS: 597-52-4 Cat. No.: T107269 Formula: C₆H₁₆OSi Peso molecolare: 132.28 Beilstein Registry Number: 1732848 Numero EC: 209-903-6 PubChem CID: 69005

GRADE & PURITY ≥97%

Synonyms

EINECS 209-903-6 | D92567 | SCHEMBL28729 | MFCD00042640 | Triethyl(hydroxy)silane | Triethylsilanol | triethyl-silanol | Silanol, triethyl- | DTXSID4060498 | Triethylsilanol, 97% | T2017 | AKOS006222293 | Hydroxytriethylsilane | E4HY4NF4Z6 | FT-0719536 |

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinonimi

EINECS 209-903-6 | D92567 | SCHEMBL28729 | MFCD00042640 | Triethyl(hydroxy)silane | Triethylsilanol | triethyl-silanol | Silanol, triethyl- | DTXSID4060498 | Triethylsilanol, 97% | T2017 | AKOS006222293 | Hydroxytriethylsilane | E4HY4NF4Z6 | FT-0719536 |

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 488184192
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184192
• Sorrisi canonici: CC[Si](CC)(CC)O
• IUPAC Name: triethyl(hydroxy)silane
• InChIKey: WVMSIBFANXCZKT-UHFFFAOYSA-N
• INCHI: 1S/C6H16OSi/c1-4-8(7,5-2)6-3/h7H,4-6H2,1-3H3
• Isomeri SMILES: CC[Si](CC)(CC)O
• WGK Germania: 1
• PubChem CID: 69005
• Numero UN: 1987
• Peso molecolare: 132.28
• Beilstein: 1732848
• Reaxy-Rn: 1732848

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Organoheterosilanes
          • Level6 Trialkylheterosilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Organoheterosilanes
• Direct Parent: Trialkylheterosilanes
• Alternative Parents: Trialkylsilanols Organic metalloid salts Organic oxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkylheterosilane - Trialkylsilanol - Organic metalloid salt - Silanol - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as trialkylheterosilanes. These are organoheterosilanes, bearing a silicon atom linked to three alkyl groups and one heteroatom.
• 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

Proprietà chimiche e fisiche

• Solubilità: Solubility in water: Practically insoluble
• Indice di rifrazione: 1.433
• Punto di infiammabilità (°F): 134.6 °F
• Punto di infiammabilità (°C): 57 °C
• Punto di ebollizione (°C): 158°C
• Peso molecolare: 132.280 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 132.097 Da
• Monoisotopic Mass: 132.097 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 51.300
• 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

Riferimenti

1. Yang Liu, Qi Lin, Xu Long, Shuting Zhang, Hong Dong, Yanjiang Song, Chuan Wu.  (2024)  Effect of segment structure of monotrimethoxysilylethyl-terminated asymmetric polysiloxanes on the thermal management performance of AlN-filled silicone pastes.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2024.105889]

2. Jiahao Lai, Bing Liu, Guihong Xiong, Qian Luo, Shuilin Song, Junxi Jiang, Hongyi Wei, Junwen Wang.  (2024)  Inhibitory mechanism of 4-ethyl-1,2-dimethoxybenzene produced by Streptomyces albidoflavus strain ML27 against Colletotrichum gloeosporioides.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:39277399] [10.1016/j.pestbp.2024.106086]

Domande frequenti

What is the purity of this product?

This product is supplied at ≥97% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at 2–8 °C. Refrigerated storage is required to maintain the specified shelf life.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 597-52-4, the molecular formula is C6H16OSi, and the molecular weight is 132.28 g/mol. InChIKey WVMSIBFANXCZKT-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.