CompoundList

Fomesafen

Also known as Fomesafene, 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide, 5-(2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-N-mesyl-2-nitrobenzamide

Fomesafen chemical structure, C15H10ClF3N2O6S, CAS 72178-02-0
2D chemical structure

Key facts

What buyers check first

Appearance
White crystalline solid
Melting point
220 °C
Boiling point
100.6 °C
Density
1.28 g/cm³ at 20 °C
Solubility
In water, 50 mg/L at 20 °C
HS code
293590
Category
Herbicides
Illustrative photo, colourless crystals in small glass vials on a laboratory bench
Typical packagingIllustrative packaging image, not the actual product

What is Fomesafen?

Plain description, key identifiers and synonyms

Fomesafen is an N-sulfonylcarboxamide that is N-(methylsulfonyl)benzamide in which the phenyl ring is substituted by a nitro group at position 2 and a 2-chloro-4-(trifluoromethyl)phenoxy group at position 5. A protoporphyrinogen oxidase inhibitor, it was specially developed for use (generally as the corresponding sodium salt, fomesafen-sodium) for post-emergence control of broad-leaf weeds in soya. It has a role as a herbicide, an agrochemical and an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor. It is a member of phenols, an aromatic ether, a C-nitro compound, an organofluorine compound, a member of monochlorobenzenes and a N-sulfonylcarboxamide. It is a conjugate acid of a fomesafen(1-).

Identifiers

Registry numbers, names and line notations, tap to copy

IUPAC name
5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-methylsulfonyl-2-nitrobenzamide
CAS number
72178-02-0 CAS number cross-checked
EC number
276-439-9
Molecular formula
C15H10ClF3N2O6S
UNII
M0A3U4CDTF
MDL number
MFCD01632756
InChIKey
BGZZWXTVIYUUEY-UHFFFAOYSA-N
InChI
InChI=1S/C15H10ClF3N2O6S/c1-28(25,26)20-14(22)10-7-9(3-4-12(10)21(23)24)27-13-5-2-8(6-11(13)16)15(17,18)19/h2-7H,1H3,(H,20,22)
SMILES (canonical and isomeric)
CS(=O)(=O)NC(=O)C1=C(C=CC(=C1)OC2=C(C=C(C=C2)C(F)(F)F)Cl)[N+](=O)[O-]

Synonyms

  • Fomesafene
  • 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide
  • 5-(2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-N-mesyl-2-nitrobenzamide
  • 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide
  • Benzamide, 5-(2-chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitro-
  • 5-(2-chloro-4-(trifluoromethyl)-phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide
  • Reflex
  • 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-methylsulfonyl-2-nitrobenzamide
  • Flex, Flexstar, PP021, Reflex
  • Fomesafene [ISO-French]
  • 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulphonyl)-2-nitrobenzamide
  • 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-N-methylsulfonyl-2-nitrobenzamide
  • 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methanesulfonyl)-2-nitrobenzamide
  • 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulphonyl)-2-nitrobenzamide
  • C15H10ClF3N2O6S
  • Fomesafen (Standard)
  • 5-(2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyloxy)-N-methylsulphonyl-2-nitrobenzamide
  • 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-methylsulfonyl-2-nitro-benzamide
  • Fomesafen 10 microg/mL in Acetonitrile
  • Fomesafen, PESTANAL(R), analytical standard
  • 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-mesyl-2-nitrobenzamide
  • 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitro-N-methanesulphonyl benzamide
  • 5-(2chloro-4-trifluoromethylphenoxy)-2-nitro-N-methansulphonyl benzamide
  • 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-N-methanesulfonyl benzamide
  • N-methylsulfonyl-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-benzamide
Show all 27 synonyms
  • 5-[2-chloro-4-(trifiuoromethyl)phenoxyl]-N-(methylsulphony)-2-nitrobenzamide
  • 5-[2-chloro-4-(trifluoromethyl)phenoxyl]-N-(methylsulphonyl)-2-nitrobenzamide

Physical and chemical properties

Measured values and descriptors computed from the structure

Physical and chemical properties

Measured values, check the supplier specification for your grade

Appearance
White crystalline solidexp.
Melting point
220 °Cexp.
Boiling point
100.6 °Cexp.
Density
1.28 g/cm³ at 20 °Cexp.
Solubility
In water, 50 mg/L at 20 °Cexp.
Vapour pressure
<4 × 10⁻³ mPa /<3.0 × 10⁻⁸ mm Hg/ at 20 °Cexp.

Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.

Computed descriptors

Calculated from the structure, useful for screening and formulation

Molecular weight
438.77 g/molcalc.
Exact mass
437.99 Dacalc.
LogP (octanol/water)
3.75calc.
Topological polar surface area
115.6 Ųcalc.
Hydrogen bond donors
1calc.
Hydrogen bond acceptors
6calc.
Rotatable bonds
5calc.
Heavy atoms
28calc.
Rings
2calc.
Aromatic rings
2calc.
Fraction sp3 carbons
0.13calc.
Formal charge
0calc.
Stereocentres
0calc.
Lipinski rule of five
Passes (0 violations)calc.

Calculated for screening. Confirm critical figures with the supplier.

Murcko scaffold

The ring system that remains when every side chain is removed

Murcko scaffold of this chemical, c1ccc(Oc2ccccc2)cc1

c1ccc(Oc2ccccc2)cc1

2 rings, 13 atoms, the Diphenyl ether ring system.

9,579 other chemicals share this scaffold

Safety and hazards

GHS classification summary, not a safety data sheet

GHS signal word
Warning
GHS07: Harmful or irritant
Harmful or irritant

Hazard statements

  • H302Harmful if swallowed.
Precautionary statements (5)
  • P264Wash skin thoroughly after handling.
  • P270Do not eat, drink or smoke when using this product.
  • P301 + P317If swallowed: Get medical help.
  • P330Rinse mouth.
  • P501Dispose of contents and container in accordance with local regulations.

GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.

Full safety data and first aid

Fomesafen suppliers

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Where suppliers are based

94 suppliers in 16 countries

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Fomesafen price

Indicative price range per kg from live supplier offers

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Uses and applications

What the substance is used for, by industry and function

Postemergence herbicide, over the top, on soybeans.

Field experiments were conducted from 1991 to 1993 to evaluate eclipta, Eclipta prostrate L., control and peanut, Arachis hypogaea L., response to herbicide treatments. Formesafen (5-(2-chloro-4-(trifluoromethyl)phenoxy)-N-(methylsulfonyl)-2-nitrobenzamide) applied at cracking was the only preemergence-applied herbicide which provided season-long control (>84%). Herbicides applied postemergence were more effective when the eclipta was less than 5 cm in height. Minor peanut injury was observed at the early season rating from several herbicides, however, all injury had disappeared by the late season rating. Eclipta control did not consistently improve peanut pod yield.

Roles

  • agrochemical
  • enzyme inhibitor
  • herbicide
  • pesticide

Functional uses

  • Biocide

How it is made

Fomesafen is manufactured by reaction of 2-chloro-4-trifluoromethylphenolate with 4-chloro-N-methylsulfonyl-2-nitrobenzamide.

Acifluorfen + ammonia + methanesulfonyl chloride (amide formation/sulfonamide formation).

Regulatory status

Inventories, regulations and trade controls that list this substance

Europe

  • EU harmonised classification (CLP Annex VI)
    Index no: 604-040-00-5

HS code and trade data

Customs classification and reported world trade statistics

Global trade

World import and export statistics for the HS code Fomesafen is traded under.

HS 2935.90Indicative HS code

Sulphonamides, other

World exports in 2024
$5.64B
−11.0% vs 2023, imports $8.56B
2019 to 2024
Top exporters
  1. Ireland43.1%
  2. China12.0%
  3. India * partner reported9.5%
Top importers
  1. United States23.6%
  2. Slovenia19.1%
  3. Spain11.7%

* Partner reported figures, a lower bound.

Reported customs values in USD, not prices.Full trade data

The HS code shown for Fomesafen is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.

Frequently asked questions

Quick answers about Fomesafen, based on the data on this page

What is Fomesafen?

Fomesafen is an N-sulfonylcarboxamide that is N-(methylsulfonyl)benzamide in which the phenyl ring is substituted by a nitro group at position 2 and a 2-chloro-4-(trifluoromethyl)phenoxy group at position 5.

What is the CAS number of Fomesafen?

The CAS registry number of Fomesafen is 72178-02-0.

What is the molecular formula and weight of Fomesafen?

The molecular formula of Fomesafen is C15H10ClF3N2O6S and its molar mass is 438.77 g/mol.

What is Fomesafen used for?

Postemergence herbicide, over the top, on soybeans. Field experiments were conducted from 1991 to 1993 to evaluate eclipta, Eclipta prostrate L., control and peanut, Arachis hypogaea L., response to herbicide treatments.

Is Fomesafen hazardous?

Fomesafen carries the GHS signal word "Warning". Main hazards: harmful if swallowed. This summary is not an SDS, always read the supplier safety data sheet.

What is the HS code of Fomesafen?

Fomesafen is usually classified under HS code 293590 (Sulphonamides, other). This is indicative, confirm it with your customs broker before shipping.

Where can I buy Fomesafen?

CompoundList lists 94 suppliers of Fomesafen in Brazil, China, United States, India and 12 more. Send one free request to get and compare quotes. Your contact details stay private until you accept a quote.

Where can I buy Fomesafen in India?

4 suppliers in India list Fomesafen on CompoundList. Filter the suppliers list by country and send a request to compare prices, grades and delivery times.

What is the price of Fomesafen?

Suppliers quote Fomesafen on request because prices depend on grade, purity, quantity and destination. A free request on CompoundList gets you several quotes to compare.

Guides for buyers

Practical guides that help when you source, ship or handle Fomesafen

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Data last updated 7 Oct 2026. Details may have changed, please confirm them with the supplier. Report an error on this page
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