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Tetrahydrofuran(THF) - Ultra dry, ≥99.9%, H2O≤50ppm, No stabilizer, high purity , CAS No.109-99-9

    Grade & Purity:
  • Ultra dry
  • ≥99.9%
  • H2O≤50ppm, No stabilizer
In stock
Item Number
T1373930
Grouped product items
SKU Size
Availability
Price Qty
T1373930-100ml
100ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$69.90
T1373930-500ml
500ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$239.90

Basic Description

Specifications & Purity Ultra dry, ≥99.9%, H2O≤50ppm, No stabilizer
Storage Temp Protected from light,Room temperature,Argon charged
Shipped In Normal
Grade Ultra dry
Product Description

Tetrahydrofuran (THF) is a saturated cyclic ether that is mainly used as an organic solvent. When stored for a long time, it forms organic peroxides. This process can be inhibited by adding butylhydroxytoluene (BHT) as a stabilizer. BHT removes free radicals needed to form peroxides. It is a key fragment of various natural products (polyether antibiotics). THF can form double hydrates with hydrogen sulfide, and its crystal structure has been studied by three-dimensional single crystal method.
Application:
Dried tetrahydrofuran (THF) has been used to synthesize dichloride {bis [1,1 ',1 "-(phosphine triyl) tripiperidine] palladium [(P(NC5H10)3)2Pd(Cl)2], which is widely used as a catalyst in Heck reactions. It has been used as a Heck cross-coupling reaction medium for various aryl bromine and olefin.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Tetrahydrofurans
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Tetrahydrofurans
Alternative Parents Oxacyclic compounds  Dialkyl ethers  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Tetrahydrofuran - Oxacycle - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
Description 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 saturated organic heteromonocyclic parent - cyclic ether - oxolanes

Names and Identifiers

IUPAC Name oxolane
INCHI InChI=1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChIKey WYURNTSHIVDZCO-UHFFFAOYSA-N
Smiles C1CCOC1
Isomeric SMILES C1CCOC1
WGK Germany 1
RTECS LU5950000
PubChem CID 8028
UN Number 2056
Packing Group II
Molecular Weight 72.11
Beilstein 102391
Reaxy-Rn 102391

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility Soluble in most organic solvents such as water, ethanol, ether, acetone, benzene, etc.
Sensitivity Light sensitive,moisture sensitive
Refractive Index 1.407
Flash Point(°C) -17℃
Boil Point(°C) 66°C
Melt Point(°C) -108.5°C
Molecular Weight 72.110 g/mol
XLogP3 0.500
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 0
Exact Mass 72.0575 Da
Monoisotopic Mass 72.0575 Da
Topological Polar Surface Area 9.200 Ų
Heavy Atom Count 5
Formal Charge 0
Complexity 22.800
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

Solution Calculators

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