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498203

3,3,3-Trifluoropropionic acid

98%

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About This Item

Linear Formula:
CF3CH2CO2H
CAS Number:
2516-99-6
Molecular Weight:
128.05
NACRES:
NA.22
PubChem Substance ID:
24873178
UNSPSC Code:
12352100
MDL number:
MFCD00153292
Assay:
98%
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Quality Level

200

assay

98%

refractive index

n20/D 1.333 (lit.)

bp

145 °C/746 mmHg (lit.)

mp

9.7 °C (lit.)

density

1.45 g/mL at 25 °C (lit.)

functional group

carboxylic acid, fluoro

SMILES string

OC(=O)CC(F)(F)F

InChI

1S/C3H3F3O2/c4-3(5,6)1-2(7)8/h1H2,(H,7,8)

InChI key

KSNKQSPJFRQSEI-UHFFFAOYSA-N

Application

3,3,3-Trifluoropropionic acid may be used in the synthesis of:
  • 2,2,2-trifluoroethyl 3,3,3-trifluoroprionate
  • ethyl 3,3,3-trifluoroprionate
  • N-trifluoropropionyl-D-mannosamine
  • 3,3,3-trifluoropropanoyl chloride

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

198.0 °F - closed cup

flash_point_c

92.22 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9537
BCCN2687
BCCJ8851
BCCH2103
BCCD1734

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Synthesis of ethyl 3,3,3-trifluoropropionate from 2-bromo-3,3,3-trifluoropropene.
Inoue M, et al.
Journal of Fluorine Chemistry, 167, 135-138 (2014)
Bi-phobic cellulose fibers derivatives via surface trifluoropropanoylation.
Cunha AG, et al.
Langmuir, 23(21), 10801-10806 (2007)
Yanbin Pan et al.
Carbohydrate research, 339(12), 2091-2100 (2004-07-29)
N-Acetyl-D-neuraminic acid (NeuNAc) aldolase is an important enzyme for the metabolic engineering of cell-surface NeuNAc using chemically modified D-mannosamines. To explore the optimal substrates for this application, eight N-acyl derivatives of D-mannosamine were prepared, and their accessibility to NeuNAc aldolase
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Global Trade Item Number

SKUGTIN
498203-25ML04061836692582
498203-5ML04061836692599