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33603

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Pentadecafluorooctanoic acid solution

100 μg/mL in methanol, analytical standard

Synonym(s):

PFAS, PFOA, Perfluorocaprylic acid solution, Perfluorooctanoic acid solution

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About This Item

Linear Formula:
CF3(CF2)6COOH
CAS Number:
Molecular Weight:
414.07
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Agency

suitable for ASTM® 7968
suitable for ASTM® 7979
suitable for DIN 38407-42
suitable for EPA 1633
suitable for EPA 533
suitable for EPA 537.1
suitable for EPA 8327
suitable for EPA ACB B21-02
suitable for EPA ACB B23-05b
suitable for EPA OTM-45
suitable for ISO 21675 2019
suitable for ISO 25101

reg. compliance

suitable for FDA C-010.02

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

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)F

InChI

1S/C8HF15O2/c9-2(10,1(24)25)3(11,12)4(13,14)5(15,16)6(17,18)7(19,20)8(21,22)23/h(H,24,25)

InChI key

SNGREZUHAYWORS-UHFFFAOYSA-N

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Application

Pentadecafluorooctanoic acid solution may be used as an ion-pairing agent in the determination of chlorhexidine in body fluids and pharmaceutical preparations, using high performance liquid chromatography(HPLC). It may also be used as an additive in the extraction of potassium ion in aqueous solution using supercritical carbon dioxide.
Pentadecafluorooctanoic acid solution may be used as an ion-pairing reagent in the development of a chromatographic method for the separation and determination of underivatized proteinic amino acids using liquid chromatography with evaporative light scattering detection (LC-ELSD) and atmospheric pressure ionization-mass spectrometry (LC-API-MS), respectively.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

The customer needs to make sure that the standard is homogeneous, this can be achieved by shaking, vortexing , or sonicating the ampoule before opening the ampoule. Care should be taken when opening the ampoule to avoid any injuries from the broken glass.
The standard should be transferred to a clean and appropriate vial or flask using clean pipettes or micro pipettes. The vial should be immediately capped to avoid any loss or evaporation of the solvent.
After opening the ampoule, the standard should not be stored or kept in the ampoule. To preserve the integrity of the product, the standard should be transferred to an appropriate vial that must be capped and stored according to the recommendation on the Certificate of Analysis.

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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High-performance liquid chromatographic method for the determination of chlorhexidine
Huston.EC, et al.
Journal of Chromatography A, 237, 457-464 (1982)
Perfluorocarboxylic acid counter ion enhanced extraction of aqueous alkali metal ions with supercritical carbon dioxide
Mochizuki S, et al.
Analyst, 124, 1507-1511 (1999)
Determination of 20 underivatized proteinic amino acids by ion-pairing chromatography and pneumatically assisted electrospray mass spectrometry.
Chaimbault P, et al.
Journal of Chromatography A, 855(1), 191-202 (1999)
Anne Vested et al.
Environmental health perspectives, 121(4), 453-458 (2013-01-31)
Perfluorinated alkyl acids (PFAAs), persistent chemicals with unique water-, dirt-, and oil-repellent properties, are suspected of having endocrine-disrupting activity. The PFAA compounds perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) are found globally in humans; because they readily cross the
Mei-Huei Chen et al.
Epidemiology (Cambridge, Mass.), 24(6), 800-808 (2013-09-17)
Epidemiologic data regarding the potential neurotoxicity of perfluorinated compounds (PFCs) are inconclusive. We investigated the associations between in utero exposure to perfluorooctanoic acid (PFOA) and perfluorooctyl sulfonate (PFOS) and early childhood neurodevelopment. We recruited 239 mother-infant pairs in northern Taiwan

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