Structure of 2,2,3,3-Tetrafluoro-1,4-butanediol CAS 425-61-6

Iden­ti­fi­ca­tion

CAS Num­ber

425-61-6

Name

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

Syn­onyms

1,4-Butanediol, 2,2,3,3-tetrafluoro-
[Index name – gen­er­at­ed by ACD/​Name]
2,2,3,3-Tetrafluor-1,4-butandiol
[Ger­man]
[IUPAC name – gen­er­at­ed by ACD/​Name]
2,2,3,3-Tetrafluoro-1,4-butanediol
[IUPAC name – gen­er­at­ed by ACD/​Name]
2,2,3,3-Tétrafluoro-1,4-butanediol
[French]
[IUPAC name – gen­er­at­ed by ACD/​Name]
2,2,3,3-Tetrafluorobutane-1,4-diol
2,2,3,3-Tetrafluorobutanediol
Tetrafluoro-1,4-butanediol

SMILES

OCC(F)(F)C(F)(F)​CO

Std­InChI

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

Std­InChIKey

CDZXJJOGD­­CLNKX-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C4H6F4O2

Mol­e­c­u­lar Weight

162.082

MDL Num­ber

MFCD00042375

Prop­er­ties

Appear­ance

White sol­id

Safe­ty Data

Per­son­al Pro­tec­tive Equipment

Eye­shields, Gloves, type N95 (US)

WGK Ger­many

3

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 2,2,3,3-Tetrafluoro-1,4-butanediol CAS 425-61-6

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Met­al Impurities

≤500ppb

Shelf Life

2 years

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

1.Fluorinated Polyurethanes : Used as a func­tion­al build­ing block in the syn­the­sis of seg­ment­ed polyurethanes and per­flu­o­ropoly­ether-mod­­i­­fied polyurethanes. 2.Fluorinated Poly­esters and Spe­cial­ty Poly­mers : Serves as a difunc­tion­al monomer or inter­me­di­ate for intro­duc­ing flu­o­ri­nat­ed seg­ments into poly­mer struc­tures. 3.Electronic Mate­ri­als Devel­op­ment : Poten­tial­ly suit­able as a high-puri­­ty inter­me­di­ate for devel­op­ing spe­cial­ty flu­o­ri­nat­ed poly­mers, func­tion­al coat­ings, and oth­er advanced mate­ri­als for elec­tron­ic appli­ca­tions, sub­ject to appli­­ca­­tion-spe­­cif­ic validation.

Key Advan­tages

1.High Chem­i­cal Puri­ty : Helps min­i­mize inter­fer­ence from unwant­ed com­po­nents dur­ing syn­the­sis and poly­mer­iza­tion. 2.Fluorinated Mol­e­c­u­lar Struc­ture : The pres­ence of diflu­o­ri­nat­ed car­bon units pro­vides oppor­tu­ni­ties to tai­lor sur­face prop­er­ties, chem­i­cal resis­tance, and oth­er mate­r­i­al char­ac­ter­is­tics. 3.Two Reac­tive Hydrox­yl Groups : Enables incor­po­ra­tion into poly­mer back­bones through suit­able poly­mer­iza­tion and func­tion­al­iza­tion reac­tions. 4.Low Met­al Impu­ri­ties : When sup­port­ed by ana­lyt­i­cal data, low met­al con­t­a­m­i­na­tion can help meet the puri­ty require­ments of elec­tron­ic-mate­r­i­al syn­the­sis. 5.Low Mois­ture Con­tent : Con­trolled water con­tent helps improve process con­sis­ten­cy in mois­­ture-sen­si­­tive reac­tions. 6.Consistent Qual­i­ty : Tight con­trol of puri­ty and impu­ri­ties sup­ports repro­ducible syn­the­sis and sta­ble down­stream mate­r­i­al performance.

This prod­uct is devel­oped by our R&D com­pa­ny Warshel Chem­i­cal Ltd (https://​www​.warshel​.com/).

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