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406449

Sigma-Aldrich

Tricosafluorododecanoic acid

95%

Synonym(s):

Perfluorododecanoic acid, Perfluorolauric acid

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About This Item

Linear Formula:
CF3(CF2)10CO2H
CAS Number:
307-55-1
Molecular Weight:
614.10
Beilstein:
1811257
EC Number:
206-203-2
MDL number:
MFCD00198081
UNSPSC Code:
12352106
PubChem Substance ID:
24865376
NACRES:
NA.22

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

Signal Word

Danger

Hazard Classifications

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

Target Organs

Liver

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM7617
MKCL4881
MKCG1398
MKCC7984
MKBX1697V

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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
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
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
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
Fengmei Cao et al.
Journal of chromatography. A, 1516, 42-53 (2017-08-22)
This work describes a novel method for the synthesis of molecularly imprinted polymers (MIPs) using 2-(trifluoromethyl) acrylic acid (TFMAA) and 4-vinyl pyridine (4-Vpy) as binary functional monomers, perfluorooctanoic acid (PFOA) as template, and ethyleneglycol dimethacrylate (EGDMA) as cross-linker in the
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