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567191

2,2,3,3-Tetrafluoro-1,4-butanediol

Name: 2,2,3,3-Tetrafluoro-1,4-butanediol
Brand: ALDRICH

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:

425-61-6

Molecular Weight:

162.08

NACRES:

NA.22

PubChem Substance ID:

24880351

UNSPSC Code:

12352100

MDL number:

MFCD00042375

Form:

solid

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Properties

form

solid

Quality Level

100

bp

110-112 °C/13 mmHg (lit.)

mp

77-82 °C (lit.)

functional group

fluoro, hydroxyl

SMILES string

OCC(F)(F)C(F)(F)CO

InChI

1S/C4H6F4O2/c5-3(6,1-9)4(7,8)2-10/h9-10H,1-2H2

InChI key

CDZXJJOGDCLNKX-UHFFFAOYSA-N

Description

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

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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"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)

"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)

"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)

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Global Trade Item Number

SKU	GTIN
567191-5G	04061832287829