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Safety Information

177814

Sigma-Aldrich

1,1,1-Trifluoro-2-iodoethane

99%

Synonym(s):

2,2,2-Trifluoroethyl iodide, 2-Iodo-1,1,1-trifluoroethane

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About This Item

Linear Formula:
CF3CH2I
CAS Number:
353-83-3
Molecular Weight:
209.94
Beilstein:
1733201
EC Number:
206-541-0
MDL number:
MFCD00001082
UNSPSC Code:
12352100
PubChem Substance ID:
24850691
NACRES:
NA.22
form:
liquid
Assay:
99%

vapor pressure

3.96 psi ( 20 °C)

Quality Level

100

Assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.401 (lit.)

bp

54.8 °C (lit.)

density

2.13 g/mL at 25 °C (lit.)

functional group

fluoro
iodo

storage temp.

2-8°C

SMILES string

FC(F)(F)CI

InChI

1S/C2H2F3I/c3-2(4,5)1-6/h1H2

InChI key

RKOUFQLNMRAACI-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

177814-500G:
177814-25G:4548173986081
177814-5G:4548173986098
177814-BULK:
177814-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
STBL4389
STBK5186
STBJ7465
STBJ7213
0000007664

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M P Bouche et al.
Clinical chemistry, 47(2), 281-291 (2001-02-13)
During low-flow or closed-circuit anesthesia with the fluorinated inhalation anesthetic sevoflurane, compound A, an olefinic degradation product with known nephrotoxicity in rats, is generated on contact with alkaline CO(2) adsorbents. To evaluate compound A formation and thus potential sevoflurane toxicity
Apeng Liang et al.
Chemical communications (Cambridge, England), 48(66), 8273-8275 (2012-07-13)
The cross-coupling reactions of 1,1,1-trifluoro-2-iodoethane with aryl and heteroaryl boronic acid esters have been successfully achieved. The new protocol allows for a convenient introduction of trifluoroethyl groups into a variety of aryl and heteroaryl moieties under mild conditions.
Roberto Morales-Cerrada et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(1), 296-308 (2018-09-20)
Thermal decarbonylation of the acyl compounds [Mn(CO)5 (CORF )] (RF =CF3 , CHF2 , CH2 CF3 , CF2 CH3 ) yielded the corresponding alkyl derivatives [Mn(CO)5 (RF )], some of which have not been previously reported. The compounds were fully

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