374334
1,1,1,2-Tetrafluoroethane
≥99%
Synonym(s):
HFC-134a
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About This Item
Linear Formula:
FCH2CF3
CAS Number:
Molecular Weight:
102.03
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥99%
bp
−26.5 °C (lit.)
SMILES string
FCC(F)(F)F
InChI
1S/C2H2F4/c3-1-2(4,5)6/h1H2
InChI key
LVGUZGTVOIAKKC-UHFFFAOYSA-N
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General description
1,1,1,2-Tetrafluoroethane is used as a trifluorovinylating agent in organic synthesis. It is identified as a potential refrigerant used in place of chlorofluorocarbons. 1,1,1,2-Tetrafluoroethane can also be used as a solvent and medical propellant for a wide range of applications. It is used to extract materials of natural origin like natural flavors, fragrances, and nutraceuticals.
Application
1,1,1,2-Tetrafluoroethane can be used:
- As a solvent in the preparation of cross-linked polymer microspheres through the dispersion polymerization method.
- As a porogenic solvent in the preparation of porous polymethacrylate monolith via free radical polymerization.
- In the synthesis of trifluorovinyllithium, a key intermediate for the preparation of 2-halo-2,3-dideoxy-arabinose derivatives of biological importance.
Packaging
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.
Compatible with the following:
Compatible with the following:
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Press. Gas Compr. Gas
Storage Class Code
2A - Gases
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Synthesis of porous cross-linked polymer monoliths using 1, 1, 1, 2-tetrafluoroethane (R134a) as the porogen
Hebb AK, et al.
Composites Science and Technology, 63(16), 2379-2387 (2003)
Parthiban Selvam et al.
Langmuir : the ACS journal of surfaces and colloids, 22(21), 8675-8683 (2006-10-04)
In situ high-pressure tensiometry and ab initio calculations were used to rationally design surfactants for the 1,1,1,2-tetrafluoroethane-water (HFA134a|W) interface. Nonbonded pair interaction (binding) energies (E(b)) of the complexes between HFA134a and candidate surfactant tails were used to quantify the HFA-philicity
Yongwon Seo et al.
Environmental science & technology, 38(17), 4635-4639 (2004-10-06)
A new separation method using gas hydrate formation is proposed for separating HFC-134a from gas mixtures containing N2 and HFC-134a. The feasibility of this separation method was investigated from various points of view. First, to determine the mixed hydrate stability
Polymer synthesis using hydrofluorocarbon solvents. 1. Synthesis of cross-linked polymers by dispersion polymerization in 1, 1, 1, 2-tetrafluoroethane
Wood CD, et al.
Macromolecules, 35(18), 6743-6746 (2002)
Alejandra Romero-Montero et al.
Materials science & engineering. C, Materials for biological applications, 115, 111154-111154 (2020-07-01)
Enzymatic mediated poly (gallic acid) (PGAL), a stable multiradical polyanion with helicoidal secondary structure and high antioxidant capacity, was successfully grafted to poly(ε-caprolactone) (PCL) using UV-photo induction. PCL films were prepared with several levels of roughness and subsequently grafted with
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