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Documenti fondamentali

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307424

Sigma-Aldrich

Silver heptafluorobutyrate

97%

Sinonimo/i:

Heptafluorobutyric acid silver salt

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About This Item

Formula condensata:
CF3CF2CF2CO2Ag
Numero CAS:
3794-64-7
Peso molecolare:
320.90
Numero CE:
223-266-1
Numero MDL:
MFCD00064197
Codice UNSPSC:
12352302
ID PubChem:
24858592
NACRES:
NA.23
Saggio:
97%
Stato:
powder

Saggio

97%

Stato

powder

Punto di fusione

292-294 °C (lit.)

Stringa SMILE

FC(F)(F)C(F)(F)C(F)(F)C(=O)O[Ag]

InChI

1S/C4HF7O2.Ag/c5-2(6,1(12)13)3(7,8)4(9,10)11;/h(H,12,13);/q;+1/p-1
GPNIJXACCBKBEP-UHFFFAOYSA-M

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H318

Consigli di prudenza

P280 - P305 + P351 + P338

Classi di pericolo

Eye Dam. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
07306DZ
10424LZ
06309JY
16626CZ

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V Gellrich et al.
Chemosphere, 87(9), 1052-1056 (2012-03-07)
Perfluorinated compounds (PFCs) can be detected worldwide in both, soil and water. In order to study the leaching behavior of this heterogeneous group of compounds in soil, flow-through column experiments have been conducted. Ten perfluoro carboxylates and four perfluoro sulfonates
Kaberi P Das et al.
Toxicological sciences : an official journal of the Society of Toxicology, 105(1), 173-181 (2008-05-31)
Perfluorobutyrate (PFBA) is a perfluoroalkyl acid (PFAA) found in the environment. Previous studies have indicated developmental toxicity of PFAAs (perfluorooctane sulfonate [PFOS] and perfluorooctanoate [PFOA]); the current study examines that of PFBA. PFBA/NH4(+) was given to timed-pregnant CD-1 mice by
Helena Zahradnícková et al.
Journal of separation science, 32(22), 3919-3924 (2009-10-21)
Heptafluorobutyl chloroformate (HFBCF), a recently introduced derivatization reagent, was examined in enantioseparation of amino acids (AAs) by GC. Twenty proteinogenic AAs, plus ornithine, cystine and 4-fluorophenylalanine (internal standard) were treated with the reagent and separation properties of the derivatives were
Toshio Takayanagi et al.
Talanta, 74(5), 1224-1230 (2008-03-29)
Perfluorinated surfactants of heptafluorobutylate and pentadecafluorooctanoate ions were adsorbed on an activated charcoal cartridge and decomposed with sodium biphenyl (SBP) reagent to form inorganic fluoride ion. The fluoride ion thus formed was determined by flow injection analysis (FIA) using quercetin-Zr
Andrej Frolov et al.
Analytical and bioanalytical chemistry, 392(6), 1209-1214 (2008-09-25)
Glycation is a common class of nonenzymatic posttranslational modifications relevant for several diseases and cell aging in general, such as D: -glucose-derived modifications at the epsilon-amino groups of lysine residues in blood proteins, especially albumin, immunoglobulin, and hemoglobin, for diabetic
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