Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

Safety Information

282278

Sigma-Aldrich

2,6-Difluorobenzamide

97%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
F2C6H3C(O)NH2
CAS Number:
18063-03-1
Molecular Weight:
157.12
Beilstein:
2047480
EC Number:
241-972-8
MDL number:
MFCD00007972
UNSPSC Code:
12352100
PubChem Substance ID:
24857034
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

mp

145-148 °C (lit.)

solubility

ethanol: soluble 5%, clear to turbid, colorless to light yellow

functional group

amide
fluoro

SMILES string

NC(=O)c1c(F)cccc1F

InChI

1S/C7H5F2NO/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,(H2,10,11)

InChI key

AVRQBXVUUXHRMY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

2,6-Difluorobenzamide is a major metabolite of pesticide diflubenzuron and has been quantitated by HPLC/diode-array method.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

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.

JAN Code

282278-10G:
282278-VAR:
282278-50G:
282278-BULK:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
12024JR
01915PV
05615MR
28430JQ
27330JQ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

HPLC/diode-array method for the determination of the pesticide diflubenzuron and its major metabolites 2,6-difluorobenzamide, 4-chlorophenylurea, and 4-chloroaniline in forestry matrixes.
Rodriguez E, et al.
Journal of Liquid Chromatography and Related Technologies, 21(12), 1857-1870 (1998)
J Koerts et al.
Xenobiotica; the fate of foreign compounds in biological systems, 27(8), 801-817 (1997-08-01)
1. The metabolic fate of the insecticide teflubenzuron, orally dosed to the male Wistar rat, was investigated. Particular attention was paid to the metabolic fate of the benzoyl and aniline moiety after hydrolysis of the urea bridge. 2. The 0-48-h
C Eriksson et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 30(10), 871-877 (1992-10-01)
The herbicides dichlobenil (2,6-dichlorobenzonitrile), chlorthiamid (2,6-dichlorothiobenzamide) and their environmental degradation product 2,6-dichlorobenzamide are irreversibly bound and toxic to the olfactory mucosa following single injections in mice (Brandt et al., Toxicology and Applied Pharmacology 1990, 103, 491-501; Brittebo et al., Fundamental
Varahenage R Perera et al.
Biochimica et biophysica acta, 1840(9), 2851-2861 (2014-05-14)
Gram-positive bacteria in the phylum Firmicutes synthesize the low molecular weight thiol bacillithiol rather than glutathione or mycothiol. The bacillithiol transferase YfiT from Bacillus subtilis was identified as a new member of the recently discovered DinB/YfiT-like Superfamily. Based on structural

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service