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ChemicalBook >> CAS DataBase List >>Fenarimol

Fenarimol

CAS No.
60168-88-9
Chemical Name:
Fenarimol
Synonyms
Bloc;EL-222;BLOC(R);RUBIGAN;Rimidin;FENARIMOL;RUBIGAN-4;RUBIGAN(R);RUBIGAN12EC;Fenarimol Standard
CBNumber:
CB9431616
Molecular Formula:
C17H12Cl2N2O
Molecular Weight:
331.2
MDL Number:
MFCD00055325
MOL File:
60168-88-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:36:41
Product description Number Pack Size Price
Fenarimol PESTANAL 45484 250mg $191
Fenarimol 164171 250mg $396
Fenarimol 98% CS-0064639 5mg $108
Fenarimol 98% CS-0064639 10mg $179
Fenarimol 98% CS-0064639 25mg $357
More product size

Fenarimol Properties

Melting point 117-119°C
Boiling point 0°C
Density 1.3886 (rough estimate)
vapor pressure 6.5 x 10-5 Pa at 25 °C
refractive index 1.5490 (estimate)
Flash point 0°C
storage temp. 0-6°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka 2.58
Water Solubility 14.6 mg l-1 (pH 3), 13.7 mg l-1 (pH 7), 13.8 mg l-1 (pH 10) at 25 °C
color Off-White to Light Yellow
Merck 13,3986
BRN 5972869
Henry's Law Constant 1.4×103 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
Major Application agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care
InChI 1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H
InChIKey NHOWDZOIZKMVAI-UHFFFAOYSA-N
SMILES OC(c1ccc(Cl)cc1)(c2cncnc2)c3ccccc3Cl
CAS DataBase Reference 60168-88-9(CAS DataBase Reference)
EWG's Food Scores 4
FDA UNII O088GU930Q
NIST Chemistry Reference 5-Pyrimidinemethanol, «alpha»-(2-chlorophenyl)-«alpha»-(4-chlorophenyl)-(60168-88-9)
EPA Substance Registry System Fenarimol (60168-88-9)
Pesticides Freedom of Information Act (FOIA) Fenarimol
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)Environment (GHS09)
GHS08,GHS09
Signal word  Warning
Hazard statements  H361fd-H362-H411
Precautionary statements  P202-P260-P263-P264-P273-P308+P313
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  Xn;N,N,Xn
Risk Statements  51/53-62-63-64
Safety Statements  36/37-61
RIDADR  UN 3017/3077
WGK Germany  2
RTECS  UV9279400
TSCA  TSCA listed
Storage Class 11 - Combustible Solids
Hazard Classifications Aquatic Chronic 2
Lact.
Repr. 2
Toxicity LD50 in mice, rats (mg/kg): 4500, 2500 orally (Beraud)

Fenarimol price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 45484 Fenarimol PESTANAL 60168-88-9 250mg $191 2026-04-30 Buy
Usbiological 164171 Fenarimol 60168-88-9 250mg $396 2026-06-03 Buy
ChemScene CS-0064639 Fenarimol 98% 60168-88-9 5mg $108 2026-06-04 Buy
ChemScene CS-0064639 Fenarimol 98% 60168-88-9 10mg $179 2026-06-04 Buy
ChemScene CS-0064639 Fenarimol 98% 60168-88-9 25mg $357 2026-06-04 Buy
Product number Packaging Price Buy
45484 250mg $191 Buy
164171 250mg $396 Buy
CS-0064639 5mg $108 Buy
CS-0064639 10mg $179 Buy
CS-0064639 25mg $357 Buy

Fenarimol Chemical Properties,Uses,Production

Chemical Properties

Pure product is white crystal. m.p. 117～119℃, vapor pressure 1.33×10-5Pa (25℃). Soluble in acetone, acetonitrile, benzene, methanol, chloroform and other organic solvents; insoluble in water. Stable to acid, alkali, heat, sensitive.

Uses

Fenarimol is a pyrimidine based fungicide which acts against rusts, blackspot and mildew fungi and it works by inhibiting the fungus’s biosynthesis of important steroid molecules.

Uses

Fenarimol is a broad spectrum pyrimidine carbinol fungicide with protective, curative and eradicative activities against powdery mildew (Erysiphe spp., Pudusphaera leucutricha, Uncinula necatur, Sphaerutheca spp., Leveillula spp.) and scab (Venturia spp.) in many crops. It also controls powdery mildew (Sphaerutheca pannusa) in ornamentals and Fusarium patch (Micruduccium niuale), Take-all patch (Laefisaria fuciformis), Dollar spot (Sderutina humeucavpa) and red thread (Gaeumannumyces graminis) in turf and amenity grasses.

Uses

Plant fungicide.

Definition

ChEBI: (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol is a member of the class of pyrimidines that is pyrimidin-5-ylmethanol in which one of the hydrogens attached to the carbon bearing the hydroxy group is replaced by a 2-chlorophenyl group while the other is replaced by a 4-chlorophenyl group. It is a tertiary alcohol, a member of monochlorobenzenes and a member of pyrimidines.

General Description

Pure white crystalline solid. Used as a fungicide. Irritates skin and mucous membranes.

Reactivity Profile

Fenarimol produces toxic gases when heated to decomposition.

Safety Profile

Moderately toxic by ingestion. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of Cland NOx.

Metabolic pathway

The primary dissipation mechanism of fenarimol in the environment involves photolysis on plants/soil surfaces and water. More than 80 photoproducts have been observed, resulting from the reduction of the pyrimidine ring, hydrolysis, ring migration and cleavage of the phenyl and pyrimidine ring moieties. Under laboratory conditions in the dark, fenarimol is relatively persistent in soil, but a more rapid dissipation was observed under field conditions with DT50 values of 18-140 days, attributed to photolysis of fenarimol on the soil surface. Fenarimol degrades in/on plant foliage/fruit surfaces mainly by photochemical processes. In animals, fenarimol is metabolised extensively to yield hydroxylated, cleavage and dechlorination products. The primary photolytic and metabolic pathways of fenarimol are presented in Schemes 1 and 2.

Degradation

Fenarimol(1) is stable in sterile buffered water in the dark at pH 3,6 and 9 at 25 °C, 37 °C and 52 °C for 28 days (Decker and Sullivan, 1975) but is readily degraded via photolysis. The photolytic DT50 in distilled water under natural sunlight and clear sky conditions at 40°N in mid-summer was approximately 12 hours (Day, 1975). The primary aqueous photolysis reaction involved the migration of the pyrimidine ring to one of the chlorophenyl rings, followed by the oxidation of the carbinol moiety to the corresponding ketone to yield 4-chloro-2-(5-pyrimidyl)-2'-chlorobenzophenone (2).
Fenarimol was extensively photodegraded on solid surfaces. More than 80 photodegradation products were formed when fenarimol was exposed to sunlight on a stainless steel surface for up to 200 hours (Althaus and Bewley, 1978a). All photoproducts were formed at very low levels (less than 3% each) and 14 were identified. An abbreviated photogradation pathway of fenarimol is presented in Scheme 1. These products were generated from the following reactions: the migration of the pyrimidine ring to one of the chlorophenyl rings, followed by the oxidation of the carbinol moiety to yield compound 2; cleavage of either one of the chlorophenyl (to yield 3,4) or pyrimidine rings (5,6); aryl hydroxylation of one of the chlorophenyl rings (7); carbinol dehydroxylation reaction to yield 8 and a bridged fluorene product (9) from the dechlorination reaction. Various cleavage products (carboxylic acids) derived from the chlorophenyl (10-13) and the pyrimidine moieties (14) were also observed.

103686-55-1
694-80-4
60168-88-9
Synthesis of Fenarimol from Methanone, (4-chlorophenyl)-5-pyriMidinyl- and 2-Bromochlorobenzene

Fenarimol Preparation Products And Raw materials

Global( 115)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd. 		+86-（0）57185586718 +86-13336195806 sales@capot.com China 29640 60
CONIER CHEM AND PHARMA LIMITED 		+8618523575427 sales@conier.com China 49979 58
career henan chemical co 		+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
TargetMol Chemicals Inc. 		+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32466 58
Hefei TNJ Chemical Industry Co.,Ltd. 		+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
Hebei Zhanyao Biotechnology Co. Ltd 		15369953316 +8615369953316 admin@zhanyaobio.com China 2123 58
HANGZHOU LEAP CHEM CO., LTD. 		+86-571-87711850 market18@leapchem.com China 24597 58
Henan Aochuang Chemical Co.,Ltd. 		+86-0371-63689365 +8618638391208 sales@aochuangchem.com China 9333 58
SUZHOU SENFEIDA CHEMICAL CO.,LTD 		+86-0512-83500002 +8618662433356 3899766280@qq.com China 26362 58
Shanghai Acmec Biochemical Technology Co., Ltd. 		+86-18621343501; +undefined18621343501 product@acmec-e.com China 33324 58

View Lastest Price from Fenarimol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fenarimol pictures 2025-04-04 Fenarimol
60168-88-9
 $5.00 1g 97% 100kg Henan Aochuang Chemical Co.,Ltd.
2-Chloronicotinamide pictures 2021-10-15 2-Chloronicotinamide
60168-88-9
 $10.00 1KG 99% 20 Tons Hebei Zhanyao Biotechnology Co. Ltd
Fenarimol pictures 2020-01-05 Fenarimol
60168-88-9
 $1.00 1KG 95-99% 1ton Career Henan Chemical Co
  • Fenarimol pictures
  • Fenarimol
    60168-88-9
  • $5.00
  • 97%
  • Henan Aochuang Chemical Co.,Ltd.
  • Fenarimol pictures
  • Fenarimol
    60168-88-9
  • $1.00
  • 95-99%
  • Career Henan Chemical Co
(2-Chlorophenyl)(4-chlorophenyl)5-pyrimidinylmethanol (2-Chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidinemethanol .alpha.-(2-chlorophenyl)-.alpha.-(4-chlorophenyl)-5-Pyrimidinemethanol 2,4’-dichloro-alpha-(pyrimidin-5-yl)benzhydrylalcohol 5-Pyrimidinemethanol, alpha-(2-chlorophenyl)-alpha-(4-chlorophenyl)- 2，4-Dichloro-α-(pyrimidin-5-y1)diphenylmethanol 2,4'-DICHLORO-A-(PYRIMIDIN-5-YL)DIPHENYLMETHANOL 2,4'-dichloro-alpha-(5-pyrimidinyl)benzhydryl alcohol EL-222 FENARIMOL BLOC(R) A-(2-CHLOROPHENYL)-A-(4-CHLOROPHENYL)-5-(PYRIMIDINEMETHANOL) RUBIGAN RUBIGAN(R) (±)2-(2-chlorophenyl)-2-(4-chlorophenyl)-5-pyrimidinemethanol (±)2,4-dichloro-α-(pyrimidin-5-yl)benzhydryl alcohol FENARIMOL, 100MG, NEAT FENARIMOL PESTANAL (2,4'-DICHLORO- A-(PY fenarimol (bsi,iso,ansi) RUBIGAN-4 RUBIGAN12EC .alpha.-(2-chlorophenyl)-.alpha.-(4-chlorophenyl)-5-Pyrimidinemethanol .alpha.-(2-Chlorophenyl)-.alpha.-(4-chlorophenyl)-5-pyrimidinemethanol fenarimol (ISO) 2,4'-dichloro-α-(pyrimidin-5-yl)benzhydryl alcohol alpha-(2-chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidinemethano alpha-(2-Chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidinemethanol Bloc Rimidin 2，4'-dichloro-α-(pyrimidin-5-yl) dipehenylmethanol (2-Chlorophenyl)-(4-chlorophenyl)-pyrimidin-5-yl-methanol alpha-(2-Chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidineme α-(2-Chlorophenyl)-α-(4-chlorophenyl)-5-pyrimidinemethanol α-(2-Chlorophenyl)α-(4-chlorophenyl)-5-pyrimidinemethanol Fenarimol 100mg [60168-88-9] Fenarimol Standard Fenarimol Solution, 1000ppm Bloc @100 μg/mL in MeOH Fenarimol@1000 μg/mL in Acetone 5-Pyrimidinemethanol, α-(2-chlorophenyl)-α-(4-chlorophenyl)- Fenarimol ISO 9001：2015 REACH Fenarimol in Acetone Fenarimol 100 μg/ml Acetonitrile L13430000CY FenarimoL10μg/mLin Cyclohexane L13430000EA FenarimoL10μg/mLin EthyLacetate XA13430000CY FenarimoL100μg/mLin Cyclohexane Pioglitazone Impurity 33 Fenarimol 10 μg/mL in Cyclohexane Fenarimol 100 μg/mL in Cyclohexane Fenarimol 10 μg/mL in Ethyl acetate 60168-88-9 C17H12Cl2NO FA - FLPesticides Alpha sort E-GAlphabetic F Fungicides Pesticides&Metabolites Pyrimidines Alphabetic
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