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196878

3-(Trifluoromethyl)benzaldehyde

97%

Synonym(s):

α,α,α-Trifluoro-m-tolualdehyde

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About This Item

Linear Formula:
CF3C6H4CHO
CAS Number:
454-89-7
Molecular Weight:
174.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24851803
EC Number:
207-228-1
Beilstein/REAXYS Number:
2327537
MDL number:
MFCD00003373
Assay:
97%
Form:
liquid
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Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.465 (lit.)

bp

83-86 °C/30 mmHg (lit.)

density

1.301 g/mL at 25 °C (lit.)

functional group

aldehyde, fluoro

SMILES string

[H]C(=O)c1cccc(c1)C(F)(F)F

InChI

1S/C8H5F3O/c9-8(10,11)7-3-1-2-6(4-7)5-12/h1-5H

InChI key

NMTUHPSKJJYGML-UHFFFAOYSA-N

General description

Aldol reaction of 3-(trifluoromethyl)benzaldehyde with hydroxyacetone in the aldolase antibody 38C2-ionic liquid system has been investigated.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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.

Group 4: Flammable liquids + Type 2 petroleums + Hazardous rank III + Water insoluble liquid

fsl

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB7619
SDBB4431
SDBB0649
STBK5506
STBJ1666

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Synthesis of fluorinated materials catalyzed by proline or antibody 38C2 in ionic liquid.
Kitazume T, et al.
Journal of Fluorine Chemistry, 121(2), 205-212 (2003)
Kazuhiro Takano et al.
Development, growth & differentiation, 53(1), 37-47 (2011-01-26)
This study investigated the development of Ca²(+) signaling mechanisms and their role in initiating morphogenetic cell movement in the presumptive ectoderm of Japanese newt (Cynops pyrrhogaster) during gastrulation. Histochemical staining using fluorescently labeled ryanodine and dihydropyridine probes revealed that dihydropyridine