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129046

Sigma-Aldrich

2,2,2-Trifluoroethylhydrazine solution

70 wt. % in H2O

Synonym(s):

Trifluoroethylhydrazine

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5 G
$105.45
25 G
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About This Item

Linear Formula:
CF3CH2NHNH2
CAS Number:
5042-30-8
Molecular Weight:
114.07
MDL number:
MFCD00007622
UNSPSC Code:
12352100
PubChem Substance ID:
24847884
NACRES:
NA.22

$105.45

List Price$111.00
Web-Only Promotion

Available to ship onApril 29, 2025Details

Request a Bulk Order

form

liquid

Quality Level

100

concentration

70 wt. % in H2O

refractive index

n20/D 1.361

transition temp

flash point 62 °C

density

1.294 g/mL at 25 °C

functional group

amine
fluoro
hydrazine

SMILES string

NNCC(F)(F)F

InChI

1S/C2H5F3N2/c3-2(4,5)1-7-6/h7H,1,6H2

InChI key

OPMFFAOEPFATTG-UHFFFAOYSA-N

Application

2,2,2-trifluoroethylhydrazine was added to myoglobin to study its interaction with heme protein[1]. It was also used to determine aldehydes and acetone simultaneously in water[2].
Building block for fluorinated pyridazines[3] and fluoroalkyl hydrazones of β-phosphonates.[4]

accessory

Product No.
Description
Pricing

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

143.6 °F

flash_point_c

62 °C

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKBC6609
MKBB6265
18824BU
13719LQ
11903KU

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As the popularity of body art including tattoo ink has increased, the safety associated with it has become an important interest. In this study, twenty volatile organic compounds (VOCs) and two aldehydes in tattoo inks were identified and quantified. Headspace
Synthetic Communications, 36, 2719-2719 (2006)
Karolina C Hernandes et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 36(12), 1808-1821 (2019-10-10)
Compounds with toxic potential may occur in beer, such as carbonyl compounds (acetaldehyde, acrolein, ethyl carbamate [EC] and formaldehyde) and furan derivatives [furfural and furfuryl alcohol (FA)]. The objective of this study was, for the first time, to validate a
Y S Choe et al.
The Journal of biological chemistry, 266(13), 8523-8530 (1991-05-05)
The oxidative reaction of equine myoglobin with alkylhydrazines results primarily in introduction of the alkyl group at the sterically hindered gamma-meso position. The gamma-meso adducts formed with ethyl- and n-butylhydrazine have been isolated and unambiguously identified. With high pressure liquid
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