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342041

Perfluoroheptanoic acid

≥97.0%

Synonym(s):

Tridecafluoroheptanoic acid, Perfluoroheptanoic acid

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About This Item

Linear Formula:
CF3(CF2)5CO2H
CAS Number:
375-85-9
Molecular Weight:
364.06
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
24861023
EC Number:
206-798-9
Beilstein/REAXYS Number:
1808210
MDL number:
MFCD00039604
Assay:
≥97.0%
Form:
solid
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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

Application

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

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wgk

WGK 3

pictograms

Health hazard
GHS08

signalword

Danger

target_organs

Liver

Storage Class

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

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Hazard Classifications

PBT - Repr. 1B - STOT RE 1 - vPvB

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP4024
BCCN6868
BCCN4681
BCCM3776
BCCL3152

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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
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
Huangfang Xu et al.
Environment international, 143, 105952-105952 (2020-07-28)
Long-chain per- and polyfluoroalkyl substances (PFASs) and their short-chain alternatives have been produced and used extensively in China. However, it is unclear whether these compounds contribute to the risk of gestational diabetes mellitus (GDM) in women residing in contaminated areas.
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Global Trade Item Number

SKUGTIN
342041-25G04061826754818
342041-5G04061826756270