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Key Documents

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406449

Sigma-Aldrich

Tricosafluorododecanoic acid

95%

Sinónimos:

Perfluorododecanoic acid, Perfluorolauric acid

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About This Item

Fórmula lineal:
CF3(CF2)10CO2H
Número de CAS:
307-55-1
Peso molecular:
614.10
Beilstein/REAXYS Number:
1811257
EC Number:
206-203-2
MDL number:
MFCD00198081
UNSPSC Code:
12352106
PubChem Substance ID:
24865376
NACRES:
NA.22

Quality Level

100

assay

95%

form

solid

bp

245 °C/740 mmHg (lit.)

mp

105-108 °C (lit.)

SMILES string

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

InChI

1S/C12HF23O2/c13-2(14,1(36)37)3(15,16)4(17,18)5(19,20)6(21,22)7(23,24)8(25,26)9(27,28)10(29,30)11(31,32)12(33,34)35/h(H,36,37)

InChI key

CXGONMQFMIYUJR-UHFFFAOYSA-N

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pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Lact. - Repr. 1B - STOT RE 1

target_organs

Liver

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCT2511
MKCS2326
MKCR1992
MKCM7617
MKCL4881

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Lei Wang et al.
Journal of chromatography. A, 1515, 45-53 (2017-08-15)
Ionic liquids have been used to efficiently extract a wide range of polar and nonpolar organic contaminants from water. In this study, imidazole ionic liquids immobilized on silica gel were synthesized through a chemical bonding method, and the immobilized dodecylimidazolium
B O Fagbayigbo et al.
Environmental monitoring and assessment, 190(6), 346-346 (2018-05-17)
In this study, an analytical method for the routine determination of nine perfluorinated compounds (PFCs), using ultra performance liquid chromatography coupled to a quadrupole time-of-flight mass spectrometer (UPLC-QTOF-MS), was developed, validated, and used for their assay in surface water and
Wei Zhao et al.
Journal of environmental sciences (China), 56, 272-280 (2017-06-03)
Perfluoroalkyl substances (PFASs) are a class of fluorine substituted carboxylic acid, sulfonic acid and alcohol, structurally similar to their corresponding parent compounds. Previous study demonstrated the potential endocrine disruption and reproductive toxicity of perfluorooctane sulfonic acid and perfluorooctanoic acid, two
John L Newsted et al.
Environmental toxicology and chemistry, 36(11), 3138-3147 (2017-06-20)
In 2011, poly- and perfluoroalkyl substances (PFASs) were analyzed in surface water and fish fillet samples taken from Pool 2 of the Upper Mississippi River, a 33-mile stretch inclusive of the Minneapolis/St. Paul, Minnesota (USA) metropolitan area. Approximately 100 each
Xuezi Yao et al.
Journal of chromatography. A, 1553, 7-15 (2018-04-14)
In this work, poly(1-vinylimidazole-ethyleneglycol dimethacrylate) (poly(VI-EDMA)) monolith coated stir bars were synthesized by one-pot polymerization, and they exhibited higher extraction efficiency and faster extraction dynamics for selected PFAAs than commercial ethylene glycol modified silicone (EG-silicone) and polydimethylsiloxane (PDMS) coated stir
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