Tetraglycol - UltraBio™, Ultra pure , CAS No.31692-85-0

CAS: 31692-85-0 Cat. No.: T432615 Numero EC: 608-659-1

GRADE & PURITY UltraBio™, Ultra pure

Synonyms

Glycofurol | Tetrahydrofurfuryl polyethylene glycol ether | Tetrahydrofurfuryl alcohol polyethyleneglycol ethe

Storage

Room temperature

Panoramica

Efficient solubilizer for glibenclamide (GBD)

Specifications

Sinonimi

Glycofurol | Tetrahydrofurfuryl polyethylene glycol ether | Tetrahydrofurfuryl alcohol polyethyleneglycol ethe

Specifiche e purezza

UltraBio™, Ultra pure

Meccanismi biochimici e fisiologici

Liquid glycofurol can readily transform into gel systems with excellent elasticity due to which, it can be used as a medium to dissolve water-insoluble drugs.

Condizioni di conservazione di stoccaggio

Room temperature

Grado

Ultra pure, UltraBio™

Nota

Note: Do not confuse with tetraglycol, sometimes referred to as tetraglycol.

Nomi e identificatori

Pubchem Sid

528771097

Sorrisi canonici

C1CC(OC1)COCCO

IUPAC Name

2-(oxolan-2-ylmethoxy)ethanol

InChIKey

CTPDSKVQLSDPLC-UHFFFAOYSA-N

INCHI

1S/C7H14O3/c8-3-5-9-6-7-2-1-4-10-7/h7-8H,1-6H2

Isomeri SMILES

C1CC(OC1)COCCO

WGK Germania

3

RTECS

MD0907500

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Tetrahydrofurans

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Tetrahydrofurans
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetrahydrofurans
• Alternative Parents: Oxacyclic compounds Dialkyl ethers Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Tetrahydrofuran - Oxacycle - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.
• 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

• Indice di rifrazione: 1.462
• Rotazione specifica [α]: +0.4°（C=0.5，methanol）
• Punto di infiammabilità (°F): 275.0 °F
• Punto di infiammabilità (°C): 135 °C
• Punto di fusione (°C): ≤ -100 °C
• Peso molecolare: 146.180 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 146.094 Da
• Monoisotopic Mass: 146.094 Da
• Topological Polar Surface Area: 38.700 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 84.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1