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Merck
CN

91719

Trifluoroacetic anhydride

derivatization grade (GC derivatization), LiChropur, ≥99.0% (GC)

Synonym(s):

TFAA

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About This Item

Linear Formula:
(CF3CO)2O
CAS Number:
Molecular Weight:
210.03
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-982-9
Beilstein/REAXYS Number:
746197
MDL number:
Assay:
≥99.0% (GC)
Grade:
derivatization grade (GC derivatization)
Technique(s):
gas chromatography (GC): suitable (ECD)
Bp:
39.5-40 °C (lit.)
Vapor pressure:
6.28 psi ( 20 °C)
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grade

derivatization grade (GC derivatization)

Quality Level

vapor pressure

6.28 psi ( 20 °C)

assay

≥99.0% (GC)

form

liquid

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations, reagent type: derivatization reagent
reaction type: Esterifications

technique(s)

gas chromatography (GC): suitable (ECD)

refractive index

n20/D 1.3 (lit.)

bp

39.5-40 °C (lit.)

mp

−65 °C (lit.)

density

1.511 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI

1S/C4F6O3/c5-3(6,7)1(11)13-2(12)4(8,9)10

InChI key

QAEDZJGFFMLHHQ-UHFFFAOYSA-N

Application

Learn more in the Product Information
Suitable for derivatization of amines, aryl amines, phenolic amines, primany amines, tertiary aromatic amines, amino acids, aminoalkylphosphoric acids, 2-aminoethylphosphoric acid, 1-hydroxy-2-aminoethylphosponic acid, amphetamine, beta blocker drugs, creatinine, desipramine, dopamine, glutathione, glycol (MOPEG), guanidine drugs, histidine, n-hydroxy-2-fluorenylacetamide, n-hydroxylamines, hydroxy acids, p-hydroxyamphetamine, 4-hydroxycoumarins, p-hydroxynorephedrine, hydroxysteroids, 5-hydroxytryptamine, indoles, Iodoamino acids, carbaryl and hydroxylated metabolites, metanephrine, methylphenidate, norepinephrine, normetanephrine, peptide amide, phenformin, phenols, phentermine, phenylthiohydantoin amino acid, propranolol, sulfonamides, sulfonylureas, thiamine, vanillymandelic acid, trisubstituted ureas and urea.

Other Notes

For the protection of prim. and sec. amines; derivatives are more volatile
Reagent for cabethoxy, butyl ester, n-methyl, methyl ester, di(trifluoroacetyl), hexafluoroisopropyl ester, acetyl or trifluoroacetyl phenylthihydantoins, trifluoroacetyl (2-hydroxy-2-methyl)ethyl, n-trifluoroacetyl, trifluoroacetyl (TFA), trifluoroacetamide, 4-trifluoromethyl-2, 6-diamino-1,3,5-triazineacetyl and trifluoroacetyl vanillin.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

supp_hazards

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 2

ppe

Faceshields, Gloves, Goggles

Regulatory Information

危险化学品

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Related Content


Phosphonoglycan. A major polysaccharide constituent of the amoeba plasma membrane contains 2-aminoethylphosphonic acid and 1-hydroxy-2-aminoethylphosphonic acid.
E D Korn et al.
The Journal of biological chemistry, 248(6), 2257-2259 (1973-03-25)
Mass fragmentography of creatinine proposed as a reference method.
I Björkhem et al.
Clinical chemistry, 23(11), 2114-2121 (1977-11-01)
T.W. Greene et al.
Protective Groups in Organic Synthesis null



Global Trade Item Number

SKUGTIN
91719-1ML04061837811869
91719-10ML04061833263655
91719-10X1ML04061833263693
91719-50ML04061833263716