567191
2,2,3,3-Tetrafluoro-1,4-butanediol
Synonym(s):
2,2,3,3-Tetrafluorobutanediol, NSC 95113, Tetrafluoro-1,4-butanediol
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About This Item
Linear Formula:
HOCH2CF2CF2CH2OH
CAS Number:
Molecular Weight:
162.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
InChI
1S/C4H6F4O2/c5-3(6,1-9)4(7,8)2-10/h9-10H,1-2H2
SMILES string
OCC(F)(F)C(F)(F)CO
InChI key
CDZXJJOGDCLNKX-UHFFFAOYSA-N
form
solid
bp
110-112 °C/13 mmHg (lit.)
mp
77-82 °C (lit.)
functional group
fluoro
hydroxyl
Quality Level
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Application
2,2,3,3-Tetrafluoro-1,4-butanediol may be used in the synthesis of the following:
- segmented polyurethanes(SPU 001-002)
- PFPE(perfluoro-polyether)modified segmented polyurethanes (SPU 003-006)
- 2,2,3,3-tetrafluorobutane-1,4-diyl dicarbamate
- 2,2,3,3-tetrafluorobutane-1,4-diyl dinitrate
- 2,2,3,3-tetrafluoro-4-((trimethylsilyl)methoxy)butanol
Reactant for:
Enzymic synthesis of silicone fluorinated aliphatic polyester amides
Enzymic synthesis of silicone fluorinated aliphatic polyester amides
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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"Synthesis and surface properties of environmentally responsive segmented polyurethanes"
Vaidya A and Chaudhury.KM
Journal of Colloid and Interface Science, 249(1), 235-245 (2002)
"Synthesis of nitrate ester and nitramine derivatives of polyfluoro alkyl compounds for high energy materials"
Srinivas D and Ghule.DV
Royal Society of Chemistry Advances, 6(10), 7712-7716 (2016)
"Comparison of Photocyclization Reactions of Fluoro-vs Nonfluoro-Substituted Polymethyleneoxy Donor Linked Phthalimides"
Park JH, et al.
Bulletin of the Korean Chemical Society,, 34(4), 1108-1114 (2013)
Piotr Król et al.
Colloid and polymer science, 290(10), 879-893 (2012-06-19)
The polarity of polyurethane coats was studied on the basis of the goniometric method for determination of wetting angle values, on the basis of calculated surface free energy (SFE) values by the van Oss-Good and Owens-Wendt methods, and on the
Piotr Król et al.
Colloid and polymer science, 289(15-16), 1757-1767 (2011-12-02)
WAXS, DSC and AFM methods were employed to compare phase structures of the coatings obtained from waterborne polyurethane cationomers which had been synthesised in the reaction of some diisocyanates (MDI, IPDI, TDI and HDI) with polyoxyethylene glycols (M = 600 and 2,000)
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