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Safety Information

F4807

Sigma-Aldrich

2-Fluorobenzaldehyde

97%

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About This Item

Linear Formula:
FC6H4CHO
CAS Number:
446-52-6
Molecular Weight:
124.11
Beilstein:
507155
EC Number:
207-171-2
MDL number:
MFCD00003302
UNSPSC Code:
12352100
PubChem Substance ID:
24894872
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.521 (lit.)

bp

90-91 °C/46 mmHg (lit.)

mp

−44.5 °C (lit.)

density

1.178 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1ccccc1F

InChI

1S/C7H5FO/c8-7-4-2-1-3-6(7)5-9/h1-5H

InChI key

ZWDVQMVZZYIAHO-UHFFFAOYSA-N

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Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H302,H315

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

131.0 °F - closed cup

Flash Point(C)

55 °C - closed cup

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.

FSL

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

JAN Code

F4807-VAR:
F4807-BULK:
F4807-100G:
F4807-10G:

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Certificates of Analysis (COA)

Lot/Batch Number
0000220863
0000220667
STBK6201
0000141037
0000107370

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Jiafeng Ding et al.
Environmental science and pollution research international, 25(30), 30160-30169 (2018-08-29)
Hydroxylated polybrominated diphenyl ethers (OH-PBDEs) are ubiquitous and highly toxic emerging endocrine disruptors found in surface and subsurface soils and clay deposits. Seriously, they could be easily transformed to the more toxic dioxins (PBDD/Fs) in photochemical processes and incineration, but
Yuan Chen et al.
Polymers, 11(6) (2019-06-07)
In this paper, we report chemical modifications of inulin by seven kinds of aromatic Schiff bases, which are different from their substituent groups. The obtained inulin derivatives were confirmed by FTIR, 1H NMR, and 13C NMR. Then, we studied their

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