All Photos(1)
About This Item
Linear Formula:
CF3COOD
CAS Number:
Molecular Weight:
115.03
Beilstein:
1768662
EC Number:
MDL number:
UNSPSC Code:
12142201
PubChem Substance ID:
Recommended Products
isotopic purity
99 atom % D
form
liquid
technique(s)
NMR: suitable
impurities
≤0.5000% water
water
refractive index
n20/D 1.3 (lit.)
bp
75 °C (lit.)
mp
-15 °C (lit.)
density
1.493 g/mL at 25 °C (lit.)
mass shift
M+1
SMILES string
[2H]OC(=O)C(F)(F)F
InChI
1S/C2HF3O2/c3-2(4,5)1(6)7/h(H,6,7)/i/hD
InChI key
DTQVDTLACAAQTR-DYCDLGHISA-N
Looking for similar products? Visit Product Comparison Guide
General description
Trifluoroacetic acid-d (d-TFA) is trifluoroacetic acid with hydrogen of the –OH group replaced by deuterium. It is usually added to other NMR solvents to shift the active hydrogen of organic compounds to low field. Trifluoroacetic acid is a non-oxidizing acid and a non-aqueous solvent which is miscible with many organic solvents. It has the ability to dissolve proteins and some polymers.
Application
Trifluoroacetic acid-d may be used as a 1H NMR and 13C NMR solvent.
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Homogeneous synthesis of amino-reserved chitosan-graft-polycaprolactone in an ionic liquid and the application in cell cultivation.
Yang L, et al.
Polymer International, 64(8), 1045-1052 (2015)
Synthesis and evaluation of cationically modified poly (styrene-alt-maleic anhydride) nanocarriers for intracellular gene delivery.
Alex MRA, et al.
Royal Society of Chemistry Advances, 5(28), 21931-21944 (2015)
Poly (ornithine-co-arginine-co-glycine-co-aspartic Acid): Preparation via NCA Polymerization and its Potential as a Polymeric Tumor-Penetrating Agent.
Yu H, et al.
Macromolecular Bioscience, 15(6), 829-838 (2015)
Hydrolytic degradation of cellulose-graft-poly (l-lactide) copolymers.
Yan C, et al.
Polymer Degradation and Stability, 118, 130-136 (2015)
Emeleus HJ and Sharpe AG.
Advances in inorganic chemistry and radiochemistry, 2-4 (1975)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service