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Merck
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주요 문서

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207934

Sigma-Aldrich

Tetrafluoroboric acid solution

48 wt. % in H2O

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About This Item

Linear Formula:
HBF4
CAS Number:
16872-11-0
Molecular Weight:
87.81
MDL number:
MFCD00011345
UNSPSC 코드:
12352106
PubChem Substance ID:
329752030
NACRES:
NA.21
농도:
46.0-52.0% in NaOH (titration)
48 wt. % in H2O

vapor density

3 (vs air)

Quality Level

200

vapor pressure

5 mmHg ( 20 °C)

양식

liquid

농도

46.0-52.0% in NaOH (titration)
48 wt. % in H2O

density

1.4 g/mL at 25 °C

SMILES string

F.FB(F)F

InChI

1S/BF3.FH/c2-1(3)4;/h;1H

InChI key

LEMQFBIYMVUIIG-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Tetrafluoroboric acid is used as a catalyst for the protection and deprotection reactions of various carbohydrates. It participates in the synthesis of 4-sulfonic acid phenyl diazonium tetrafluoroborate, which was required for the preparation of sulfonated graphene (SG).

애플리케이션

Tetrafluoroboric acid solution may be used as a catalyst for the hydration of aromatic haloalkynes to α-halomethyl ketones in the absence of metal catalysts. It may also be used the epoxidized soybean oil (ESBO) ring opening step of fatty acids preparation.

픽토그램

Corrosion
GHS05

신호어

Danger

유해 및 위험 성명서

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

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시험 성적서(COA)

Lot/Batch Number
MKCX0904
MKCW0550
MKCW0549
MKCV4020
MKCS5791

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COA 검색

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문서 라이브러리 방문

Tetrafluoroboric acid, an efficient catalyst in carbohydrate protection and deprotection reactions.
Albert R, et al.
Carbohydrate Research, 137, 282-290 (1985)
Polyols and polyurethanes prepared from epoxidized soybean oil ring-opened by polyhydroxy fatty acids with varying OH numbers.
Chen R, et al.
Journal of Applied Polymer Science, 132(1) (2015)
Self-assembling sulfonated graphene/polyaniline nanocomposite paper for high performance supercapacitor.
Fan T, et al.
Synthetic Metals, 199, 79-86 (2015)
Metal-free hydration of aromatic haloalkynes to a-halomethyl ketones.
Ye M, et al.
Tetrahedron Letters, 57(45), 4983-4986 (2016)
M P Dariel et al.
Dental materials : official publication of the Academy of Dental Materials, 11(3), 208-217 (1995-05-01)
The purpose of this study was to develop a new technology for preparing mercury-free metallic dental restorative materials. The novel approach relies on the cold welding of surface treated silver particles. At ambient temperature, intermetallic compound formation takes place spontaneously
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