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Merck
CN

77251

七氟丁酸酐

≥99.0% (GC)

别名:

HFAA, HFBA, 全氟丁酸酐

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线性分子式:
(CF3CF2CF2CO)2O
化学文摘社编号:
分子量:
410.06
EC Number:
206-410-8
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
856036
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assay

≥99.0% (GC)

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations, reagent type: derivatization reagent
reaction type: Esterifications, reagent type: derivatization reagent
reaction type: Silylations

technique(s)

gas chromatography (GC): suitable (ECD)

refractive index

n20/D 1.287 (lit.)

bp

108-110 °C (lit.)

mp

−43 °C (lit.)

density

1.674 g/mL at 20 °C (lit.)

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(=O)OC(=O)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C8F14O3/c9-3(10,5(13,14)7(17,18)19)1(23)25-2(24)4(11,12)6(15,16)8(20,21)22

InChI key

UFFSXJKVKBQEHC-UHFFFAOYSA-N

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Application

Suitable for the derivatization of short chain aliphatic acids (C2-C8), amino acids, amphetamines and related amines, primary and secondary amines, carbamate insecticide, carbofuran and metabolites, n-nitrosamines, peptide methyl esters, phenols, terodiline (N-t-butyl-1-methyl-3, 3-diphenylpropylamine and thyroid hormons and analogs..

Other Notes

Reagent for dideuteroheptafluorobutyl amino alcohol, heptafluorobutyryl, methyl ester, trichloroethyl ester, and trimethylsilyl ether.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mass spectrometric and gas chromatographic studies of n-heptafluorobutyryl derivatives of peptide methyl esters.
B A Andersson
Acta chemica Scandinavica, 21(10), 2906-2908 (1967-01-01)
D.R. Knapp
Handbook of Analytical Derivatization Reactions, 255-261 (1979)
R.A. Chapman and J.R. Robinson
Journal of Chromatography A, 140, 209-209 (1977)
J.F. Lawrence
Journal of Chromatography A, 123, 287-287 (1976)
Reaction of nitrosamine with fluorinated anhydrides and pyridine to form electron capturing derivatives.
J B Brooks et al.
Analytical chemistry, 44(13), 1881-1886 (1972-09-01)

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