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342041

Sigma-Aldrich

Perfluoroheptanoic acid

≥97.0%

Synonym(s):

Tridecafluoroheptanoic acid, Perfluoroheptanoic acid

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10 μG
¥3,703.16

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10 μG
¥3,703.16

About This Item

Linear Formula:
CF3(CF2)5CO2H
CAS Number:
375-85-9
Molecular Weight:
364.06
Beilstein:
1808210
EC Number:
206-798-9
MDL number:
MFCD00039604
UNSPSC Code:
12352200
PubChem Substance ID:
24861023
NACRES:
NA.22

¥3,703.16

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Quality Level

200

Assay

≥97.0%

form

solid

refractive index

n20/D 1.306 (lit.)

bp

175 °C/742 mmHg (lit.)

mp

30 °C (lit.)

density

1.792 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C7HF13O2/c8-2(9,1(21)22)3(10,11)4(12,13)5(14,15)6(16,17)7(18,19)20/h(H,21,22)

InChI key

ZWBAMYVPMDSJGQ-UHFFFAOYSA-N

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Show Differences

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This Item
SRP2056SRP2045SRP2139
PPAR γ, ligand binding domain (204-477), GST tagged human recombinant, expressed in E. coli, ≥80% (SDS-PAGE)

SRP2140

PPAR γ, ligand binding domain (204-477), GST tagged human

PPARγ, ligand binding domain (165-441) human recombinant, expressed in E. coli, ≥80% (SDS-PAGE)

SRP2056

PPARγ, ligand binding domain (165-441) human

PPAR， γ 人 recombinant, expressed in E. coli, ≥70% (SDS-PAGE)

SRP2045

PPAR， γ 人

PPAR δ, ligand binding domain (165-441), GST tagged human recombinant, expressed in E. coli, ≥80% (SDS-PAGE)

SRP2139

PPAR δ, ligand binding domain (165-441), GST tagged human

biological source

human

biological source

human

biological source

human

biological source

human

assay

≥80% (SDS-PAGE)

assay

≥80% (SDS-PAGE)

assay

≥70% (SDS-PAGE)

assay

≥80% (SDS-PAGE)

recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in E. coli

concentration

450 μg/mL

concentration

350 μg/mL

concentration

500 μg/mL

concentration

300 μg/mL

form

frozen liquid

form

frozen liquid

form

frozen liquid

form

frozen liquid

mol wt

~57.8 kDa

mol wt

~33.6 kDa

mol wt

~60 kDa

mol wt

~58.2 kDa

Application

Perfluoroheptanoic acid can be used as a reactant:
  • For the fluoroalkylation of C-H bonds of aromatic compounds using Ni/SiO2 nanocatalyst[1].
  • To synthesize biphenylyl benzoates via Mitsunobu reaction.
  • To synthesize N-perfluoracyl β-thioamides from β-thio amines in the presence of methyl chloroformate[2].

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H360D,H372

Hazard Classifications

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
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    BCCM3776
    BCCL3152
    BCCG9250
    BCCF9059
    BCCB7951

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    Bart B L Groen et al.
    The Journal of clinical endocrinology and metabolism, 101(11), 3978-3988 (2016-11-05)
    Skeletal muscle protein synthesis is highly responsive to food intake. It has been suggested that the postprandial increase in circulating insulin modulates the muscle protein synthetic response to feeding. The objective of the study was to investigate whether a greater
    Synthesis of new fluorous modular chiral ligand derivatives from amino alcohols and application in enantioselective carbon-carbon bond-forming alkylation reactions
    Sehnem J, et al.
    Tetrahedron Asymmetry, 21, 997-1003 (2010)
    Mikhail N Khrizanforov et al.
    Dalton transactions (Cambridge, England : 2003), 45(30), 11976-11982 (2016-07-08)
    We have developed Ni(III)-doped silica nanoparticles ([(bpy)xNi(III)]@SiO2) as a recyclable, low-leaching, and efficient oxidative functionalization nanocatalyst for aromatic C-H bonds. The catalyst is obtained by doping the complex [(bpy)3Ni(II)] on silica nanoparticles along with its subsequent electrooxidation to [(bpy)xNi(III)] without
    N Kudo et al.
    Chemico-biological interactions, 134(2), 203-216 (2001-04-20)
    Elimination in urine and feces was compared between four perfluorinated fatty acids (PFCAs) with different carbon chain length. In male rats, perfluoroheptanoic acid (PFHA) was rapidly eliminated in urine with the proportion of 92% of the dose being eliminated within
    Wenchao Han et al.
    Environment international, 116, 206-213 (2018-04-27)
    Perfluoroalkyl and polyfluoroalkyl substances (PFASs) have been widely detected in different populations. However, limited data is available about exposure among family members. To investigate the PFASs levels in parents and their newborns and to understand their correlation and health implications
    View All Related Papers

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