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Fenpropidin

CAS No.
67306-00-7
Chemical Name:
Fenpropidin
Synonyms
fenpropidine;TERN;patrol;SPONSOR;COLUMBIA;ro12-3049;cga114900;Fenproidin;FENPROPIDIN;Brn 1245248
CBNumber:
CB1283550
Molecular Formula:
C19H31N
Molecular Weight:
273.46
MDL Number:
MFCD28046835
MOL File:
67306-00-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-31 15:25:14

Fenpropidin Properties

Melting point 25°C
Boiling point bp0.2 117°; bp0.045 125°; bp0.032 104°
Density 0.9112 (rough estimate)
vapor pressure 1.7 x 10-2 Pa (25 °C)
refractive index 1.4900 (estimate)
storage temp. Refrigerator
solubility Chloroform, Ethyl Acetate (Slightly)
form Liquid
pka 10.1
Water Solubility 530 mg l-1 (pH 7 at 25 °C)
color Clear Colourless
Merck 13,4020
BRN 5336091
Henry's Law Constant 7.1×102 mol/(m3Pa) at 25℃, Feigenbrugel and Calvé (2021)
Major Application agriculture
environmental
InChI 1S/C19H31N/c1-16(15-20-12-6-5-7-13-20)14-17-8-10-18(11-9-17)19(2,3)4/h8-11,16H,5-7,12-15H2,1-4H3
InChIKey MGNFYQILYYYUBS-UHFFFAOYSA-N
SMILES CC(CN1CCCCC1)Cc2ccc(cc2)C(C)(C)C
CAS DataBase Reference 67306-00-7
FDA UNII 845XW54F31
NIST Chemistry Reference Fenpropidin(67306-00-7)
EPA Substance Registry System Piperidine, 1-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]- (67306-00-7)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS05,GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H302+H332-H317-H318-H335-H373-H410
Precautionary statements  P273-P280-P301+P312-P304+P340+P312-P305+P351+P338-P314
target organs Central nervous system, Respiratory system
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xn
Risk Statements  21/22-36
Safety Statements  26-36/37
RIDADR  2902
WGK Germany  3
RTECS  TM7292000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29333990
Storage Class 10 - Combustible liquids
Hazard Classifications Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Eye Dam. 1
Skin Sens. 1B
STOT RE 2
STOT SE 3

Fenpropidin price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 46017 Fenpropidin PESTANAL 67306-00-7 50mg $171 2026-04-30 Buy
ChemScene CS-0092562 Fenpropidin 99.48% 67306-00-7 5mg $43 2026-06-04 Buy
ChemScene CS-0092562 Fenpropidin 99.48% 67306-00-7 10mg $65 2026-06-04 Buy
ChemScene CS-0092562 Fenpropidin 99.48% 67306-00-7 25mg $87 2026-06-04 Buy
ChemScene CS-0092562 Fenpropidin 99.48% 67306-00-7 50mg $103 2026-06-04 Buy
Product number Packaging Price Buy
46017 50mg $171 Buy
CS-0092562 5mg $43 Buy
CS-0092562 10mg $65 Buy
CS-0092562 25mg $87 Buy
CS-0092562 50mg $103 Buy

Fenpropidin Chemical Properties, Uses, Production

Description

fenpropidine, a piperidine derivative, and spiroxamine, a dioxolanemethyleneamine derivative introduced in 1996 , belong to the same group of fungicides.

Chemical Properties

Pure phenyl rustidine is light yellow, viscous, odorless liquid. Boiling point:>250°C,70.2°C/1.1Pa.Distribution coefficient KowlgP(25°C,pH 7)=2.9,Henry's constant 10.7 Pa-m3/mol(25°C,calculated). Relative density 0.91(20℃). Solubility in water(g/m3,25℃):530(pH 7),6.2(pH 9);Freely soluble in acetone,ethanol,toluene,n-octanol,n-hexane and other organic solvents. Stable for at least 3 years in closed containers at room temperature, its aqueous solution is UV stable and not hydrolyzed. Strong base,pKa10.1, flash point 156℃.

Uses

Fenpropidin is a fungicide.

Uses

Agricultural fungicide.

Uses

Fenpropidin is both a contact and a systemic fungicide which provides effective eradicant control of powdery mildew, rusts and leaf blotch in cereal.

Production Methods

Fenpropidin is commercially synthesised through a multi-step process involving alkylation and cyclization reactions. The synthesis begins with 1-(2-methyl-3-phenylpropyl)piperidine, which is dissolved in methylene chloride and treated with concentrated sulfuric acid under cooling to maintain an internal temperature around 10 DegC. After acidification, tert-butanol is added to the mixture, which is then allowed to react at room temperature for several hours. The reaction mixture is subsequently neutralized, extracted, and purified, typically via fractional distillation using a Goodloe silver column, to yield high-purity fenpropidin.

Definition

ChEBI: A member of the class of piperidines that is N-isobutylpiperidine in which a hydrogen of one of the methyl groups is replaced by a p-tert-butylphenyl group.

Hazard

Moderately toxic by ingestion, inhalation, and skin contact.

Mechanism of action

Systemic with curative and protective action. Inhibits sterol biosynthesis in membranes.

Metabolic pathway

Limited data are available in the open literature. Information presented in this summary is abstracted from the data evaluation published by the Pesticide Safety Directorate (PSD, 1993). Fenpropidin is stable to aqueous hydrolysis and photodegradation. Hydroxylation of the piperidine ring is the primary metabolic pathway in soil and wheat plants. Hydroxylation and oxidation of one of the methyl groups of the tert-butyl moiety are the major reactions in rats and lactating goats. The primary metabolic pathways of fenpropidin are presented in Scheme 1.

Degradation

Fenpropidin (1)i s stable to hydrolytic degradation (50 °C)in the pH range of 3-9 and when exposed to UV light in pH 5 buffer solution.

Pesticide Type

Fungicide

Fenpropidin Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 93)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Syntechem Co.,Ltd info@syntechem.com China 12973 57
Sichuan Kulinan Technology Co., Ltd 400-1166-196 18981987031 cdhxsj@163.com China 11674 57
Tianjin Derchemist Science & Technology Co., Ltd. 22-58627059 13920586291 zdcomcon@126.com China 4094 50
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29977 65
Nanjing Sunlida Biological Technology Co., Ltd. 025-57798810 18652991625 sales@sunlidabio.com China 3223 55
Shanghai JONLN Reagent Co., Ltd. 400-0066400 13621662912 422131432@qq.com China 9970 55
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. 025-66028182 17714375163 yftan@aikonchem.com China 16674 50
Alta Scientific Co., Ltd. 022-6537-8550 15522853686 sales@altasci.com.cn China 4508 55
VWR(Shanghai) Co., Ltd 400-821-8006 info_china@vwr.com China 3036 75

View Latest Price from Fenpropidin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fenpropidin pictures 2026-07-15 Fenpropidin
67306-00-7
$31.00-64.00 98.58% 10g TargetMol Chemicals Inc.
Fenpropidin pictures 2019-12-25 Fenpropidin
67306-00-7
$1.00 1KG 98%HPLC 10t Career Henan Chemical Co
  • Fenpropidin pictures
  • Fenpropidin
    67306-00-7
  • $31.00-64.00
  • 98.58%
  • TargetMol Chemicals Inc.
  • Fenpropidin pictures
  • Fenpropidin
    67306-00-7
  • $1.00
  • 98%HPLC
  • Career Henan Chemical Co
TERN SPONSOR 1-(3-(4-(1,1-dimethylethyl)phenyl)-2-methylpropyl)-piperidin 1-(3-(4-(1,1-dimethylethyl)phenyl)-2-methylpropyl)piperidine 1-(3-(4-tert-butylphenyl)-2-methylpropyl)piperidine cga114900 patrol ro12-3049 FENPROPIDIN COLUMBIA (RS)-1-[3-(4-tert-butylphenyl)-2-methyl-propyl]piperidine Fenproidin FENPROPIDIN PESTANAL, 250 MG Piperidine, 1-3-4-(1,1-dimethylethyl)phenyl-2-methylpropyl- fenpropidin (bsi, iso) Fenpropidin Solution, 1000ppm Brn 1245248 Fenpropidine [iso-french] Fenpropidin 0 Fenpropidin Solution Fenpropidin@100 μg/mL in Methanol Inhibitor,Fungal,fungicide,sterol biosynthesis inhibitor,Fenpropidin,inhibit Fenpropidin Solution in Methanol Fenpropidin Solution in Acetonitrile C13537000 Fenpropidin Fenpropidin 10.0 μg/ml Cyclohexane Fenpropidin 100 μg/ml Acetonitrile XA13537000CY Fenpropidin 100μg/mLin Cyclohexan Fenpropidin in Methanol Fenpropidin in Acetonitrile Carenoprazan Impurity 5 D-trans-Chloproparthrin Fenpropidin 100 μg/mL in Cyclohexane fenpropidine 67306-00-7 C19H31N Alpha sort E-GAlphabetic F FA - FLPesticides Fungicides Others Pesticides&Metabolites