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About This Item
Linear Formula:
CF3CF2CF2COOH
CAS Number:
Molecular Weight:
214.04
EC Number:
206-786-3
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
1426882
InChI
1S/C4HF7O2/c5-2(6,1(12)13)3(7,8)4(9,10)11/h(H,12,13)
InChI key
YPJUNDFVDDCYIH-UHFFFAOYSA-N
SMILES string
OC(=O)C(F)(F)C(F)(F)C(F)(F)F
vapor density
7 (vs air)
vapor pressure
~10 mmHg ( 25 °C)
assay
≥99.0% (GC)
refractive index
n20/D 1.3 (lit.)
bp
120 °C/755 mmHg (lit.)
density
1.645 g/mL at 25 °C (lit.)
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Other Notes
This product has been replaced by 77249-SIGMA | Heptafluorobutyric acid ≥99.0% (GC)
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1A
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Yuko Murakami et al.
Organic & biomolecular chemistry, 12(48), 9887-9894 (2014-10-31)
Desmosine-CH2, an analog of the elastic tissue degradation biomarker desmosine, can be regarded as a potential internal standard for precise quantification of desmosines by LC-MS/MS. In this study, the chemical synthesis of desmosine-CH2 was completed in 22% overall yield in
Ulrika Eriksson et al.
Environmental science and pollution research international, 20(11), 7940-7948 (2013-04-17)
Diet and drinking water are suggested to be major exposure pathways for perfluoroalkyl substances (PFASs). In this study, food items and water from Faroe Islands sampled in 2011/2012 were analyzed for 11 perfluoroalkyl carboxylic acids (PFCAs) and 4 perfluoroalkane sulfonic
Jan Busch et al.
Environmental pollution (Barking, Essex : 1987), 158(5), 1467-1471 (2010-01-08)
Polyfluoroalkyl compounds (PFCs) are widely used in industry and consumer products. These products could end up finally in landfills where their leachates are a potential source for PFCs into the aqueous environment. In this study, samples of untreated and treated
Sławomir Wybraniec et al.
Journal of chromatography. A, 1216(41), 6890-6899 (2009-09-08)
Polar betacyanin pigments together with betaxanthins from ripe cactus fruits of Hylocereus polyrhizus (Cactaceae) were fractionated by means of preparative ion-pair high-speed countercurrent chromatography (IP-HSCCC) also using the elution-extrusion (EE) approach for a complete pigment recovery. HSCCC separations were operated
John L Butenhoff et al.
Reproductive toxicology (Elmsford, N.Y.), 33(4), 513-530 (2011-09-01)
Sequential 28-day and 90-day oral toxicity studies were performed in male and female rats with ammonium perfluorobutyrate (NH(4)(+)PFBA) at doses up to 150 and 30mg/kg-d, respectively. Ammonium perfluorooctanoate was used as a comparator at a dose of 30mg/kg-d in the
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