| Identification | Back Directory | [Name]
Propanil | [CAS]
709-98-8 | [Synonyms]
NOX
STAM
Wham
Propa
strel
Rogue
Erban
STAM1
Farmco
FW 734
drexel
Surpur
Dipram
Herbax
vertac
s10165
Sorpur
S 10165
propjob
Erbanil
KEM-RAY
apronox
rosanil
RICENIL
STAM(R)
Prostar
RISELECT
ROGUE(R)
Propanex
PROPANIL
Supernox
SURCOPUR
stam m-4
STAMPEDE
b-30,130
bay30130
herbax3e
herbax4e
Propanid
Grascide
prop-job
Prop job
stamlv10
synprann
Synpran N
Propanide
Propanile
propanilo
BAY 30130
Stam F-34
Chem Rice
PROPASINT
Suercopur
Propanial
zgc:55725
wu:fv75b10
bayer30130
stampede3e
Stam LV 10
herbaxlv-30
Stampede CM
SURCOPUR(R)
dcpa (jmaf)
STAM F-34(R)
Cekupropanil
stamsupernox
DKFZp686J2352
farmcopropanil
drexelprop-job
herbaxtechnical
vertacpropanil3
vertacpropanil4
montrosepropanil
Montrose propanil
crystalpropanil-4
Propanil Standard
Propanil E.C.(20%)
Dichloropropionanilide
propanil (bsi,iso,wssa)
3,4-DICHLOROPROPIONANILINE
Propanil 500mg [709-98-8]
3,4-DICHLOROPROPIONANILIDE
3,4-Dichloropropiomamilide
3',4'-Dichloropropioanilide
PROPANIL TECHNICAL TOXICANT
3',4'-DICHLOROPROPIONANILIDE
3’,4’-dichloro-propionanilid
Propionanilide, 3',4'-dichloro-
propionicacid3,4-dichloroanilide
PROPIONICACID3,4-DICHLOROANILINE
N-(3,4-Dichlorphenyl)-propionamid
propionicacid-3,4-dichloroanilide
n-(3,4-dichlorophenyl)-propanamid
N-(3,4-Dichlorophenyl)propanamide
3’,4’-dichlorophenylpropionanilide
N-(3,4-Dichlorophenyl)Propionamide
Propionic acid 3,4-dichloroanilide
Propionoic acid 3,4 dichloranilide
N-93，4-dichlorophenyl) propanamide
3,4-dichloranilidkyselinypropionove
Propanamide, N-(3,4-dichlorophenyl)-
3'.4'-Dichloropropionanilide Solution
Anti-STAM antibody produced in rabbit
PROPANIL PESTANAL (3',4'-DICHLORO- PROPI
propanil (ISO) 3',4'-dichloropropionanilide
FREE SAMPLE NCV PROPANIL 60% + MCPA 7.5% DF
3'.4'-Dichloropropionanilide 500mg [709-98-8] | [EINECS(EC#)]
211-914-6 | [Molecular Formula]
C9H9Cl2NO | [MDL Number]
MFCD00018149 | [MOL File]
709-98-8.mol | [Molecular Weight]
218.08 |
| Chemical Properties | Back Directory | [Appearance]
Propanil is a colorless solid. The technical
product is a brown crystalline solid. | [Melting point ]
92-93°C | [Boiling point ]
369.9±32.0 °C(Predicted) | [density ]
1.25 | [refractive index ]
1.5680 (estimate) | [Fp ]
100 °C | [storage temp. ]
0-6°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
13.58±0.70(Predicted) | [color ]
Dark brown, blue-black | [biological source]
rabbit | [Water Solubility ]
225mg/L(room temperature) | [Merck ]
13,7896 | [BRN ]
2365645 | [Henry's Law Constant]
1.3×101 mol/(m3Pa) at 25℃, Chao et al. (2017) | [Major Application]
agriculture
environmental | [InChI]
1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13) | [InChIKey]
LFULEKSKNZEWOE-UHFFFAOYSA-N | [SMILES]
CCC(=O)Nc1ccc(Cl)c(Cl)c1 | [LogP]
3.070 | [CAS DataBase Reference]
709-98-8 | [NIST Chemistry Reference]
Propanil(709-98-8) | [EPA Substance Registry System]
Propanamide, N-(3,4-dichlorophenyl)-(709-98-8) |
| Hazard Information | Back Directory | [Chemical Properties]
Light Brown Solid | [Uses]
Propanil is a a widely used herbicide. Propanil is used mainly to control weed growth in rice fields. | [General Description]
Colorless to brown crystals. Non corrosive. Used as an herbicide. | [Air & Water Reactions]
Hydrolyzed by acid and alkaline media. | [Reactivity Profile]
Propanil is incompatible with carbamates and organophosphates. | [Hazard]
Toxic by ingestion and inhalation.
| [Potential Exposure]
Propanil is used as a postemergent
herbicide for rice and spring wheat. A potential danger
to those involved in the manufacture, formulation, and
application of this contact herbicide. | [First aid]
If this chemical gets into the eyes, remove any
contact lenses at once and irrigate immediately for at least
15 minutes, occasionally lifting upper and lower lids. Seek
medical attention immediately. If this chemical contacts the
skin, remove contaminated clothing and wash immediately
with soap and water. Seek medical attention immediately.
If this chemical has been inhaled, remove from exposure,
begin rescue breathing (using universal precautions, includ-
ing resuscitation mask) if breathing has stopped and CPR if
heart action has stopped. Transfer promptly to a medical
facility. When this chemical has been swallowed, get medi-
cal attention. Give large quantities of water and induce
vomiting. Do not make an unconscious person vomit. | [Shipping]
UN3077 Environmentally hazardous substances,
solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous
hazardous material, Technical Name Required. | [Incompatibilities]
Incompatible with oxidizers (chlorates,
nitrates, peroxides, permanganates, perchlorates, chlorine,
bromine, fluorine, etc.); contact may cause fires or explo-
sions. Keep away from alkaline materials, strong bases,
strong acids, oxoacids, epoxides. | [Waste Disposal]
Hydrolysis in acidic or basic
media yields the more toxic substance, 3,4-dichloraniline,
and is not recommended. | [Definition]
ChEBI: Propanil is an anilide resulting from the formal condensation of the carboxy group of propanoic acid with the amino group of 3,4-dichloroaniline. It is a herbicide used for the treatment of numerous grasses and broad-leaved weeds in rice, potatoes, and wheat. It has a role as a herbicide. It is an anilide and a dichlorobenzene. It is functionally related to a 3,4-dichloroaniline. | [Production Methods]
The industrial synthesis of propanil begins with the preparation of 3,4-dichloroaniline, which serves as the aromatic amine base. This compound is reacted with propionyl chloride in the presence of an acid scavenger such as pyridine or a base like triethylamine to form the amide bond. The acylation reaction is typically carried out in organic solvents such as toluene or dichloromethane under controlled temperature conditions to ensure high yield and minimize side reactions. After the reaction is complete, the crude product is purified through crystallisation or solvent extraction. | [Agricultural Uses]
Herbicide: Propanil is a post-emergence herbicide with no residual effect. It is used against numerous grasses and broadleaved weeds in rice, potatoes, and wheat. Mixing with carbamates or organophosphorus compounds is not recommended. It is also used on wheat in a mixture with MCPA. With carbaryl, it is used in citrus crops grown in sod culture. Not approved for use in EU countries (re-submitted). Registered for use in the U.S. | [Trade name]
Cekupropanil; DCPA; N-(3,4-Dichlorophenyl) propanamide; 3',4'-Dichlorophenyl propionanilide; 3,4-Dichloropropionanilide; 3',4'-Dichloropropionanilide; Dichloropropionanilide; Dipram; DPA; NSC 31312; Propanamide, N-(3,4-Dichlorophenyl)-; Propanide; Propionanilide, 3',4'-Dichloro-; Propionic acid, 3,4-dichloroanilide | [Mechanism of action]
Selective with contact action, inhibition of photosynthesis | [Environmental Fate]
Biological. In the presence of suspended natural populations from unpolluted aquatic
systems, the second-order microbial transformation rate constant determined in the laboratory was reported to be 5 × 10–10 L/organisms-hour (Steen, 1991).
Soil. Propanil degrades in soil forming 3,4-dichloroaniline (Bartha, 1968; Bartha and
Pramer, 1970; Chisaka and Kearney, 1970; Bartha, 1971; Duke et al., 1991; Pothuluri et
al., 1991) which is further degraded by microbial peroxidases to 3,3′,4,4′-tetrachloroazobenzene (Bartha and Pramer, 1967; Bartha et al., 1968; Chisaka and Kearney, 1970),
3,3′,4,4′-tetrachloroazooxybenzene (Bartha and Pramer, 1970), 4-(3,4-dichloroanilo)-
3,3′,4,4′-tetrachloroazobenzene (Linke and Bartha, 1970) and 1,3-bis(3,4-dichlorophenyl)triazine (Plimmer et al., 1970a), propanoic acid, carbon dioxide and unidentified
products (Chisaka and Kearney, 1970). Evidence suggests that 3,3′,4,4′-tetrachloroazobenzene reacted with 3,4-dichloroaniline forming a new reaction product, namely 4-(3,4-
dichloroanilo)-3,3′,4′-trichloroazobenzene (Chisaka and Kearney, 1970). Under aerobic
conditions, propanil in a biologically active, organic-rich pond sediment underwent dechlorination at the para- position forming N-(3-chlorophenyl)propanamide (Stepp et al., 1985).
Residual activity in soil is limited to approximately 3–4 months (Hartley and Kidd, 1987).
Plant. In rice plants, propanil is rapidly hydrolyzed via an aryl acylamidase enzyme
isolated by Frear and Still (1968) forming the nonphototoxic compounds (Ashton and
Monaco, 1991) 3,4-dichloroaniline, propionic acid (Matsunaka, 1969; Menn and Still,
1977; Hatzios, 1991) and a 3′,4′-dichloroaniline-lignin complex. This complex was identified as a metabolite of N-(3,4-dichlorophenyl)glucosylamine, a 3,4-dichloroaniline saccharide conjugate and a 3,4-dichloroaniline sugar derivative (Yi et al., 1968). In a rice
field soil under anaerobic conditions, however, propanil underwent amide hydrolysis and
dechlorination at the para position forming 3,4-dichloroaniline and m-chloroaniline (Pettigrew et al., 1985). In addition, propanil may degrade indirectly via an initial oxidation
step resulting in the formation of 3,4-dichlorolacetanilide which is further hydrolyzed to
3,4-dichloroaniline and lactic acid (Hatzios, 1991). In an earlier study, four metabolites
were identified in rice plants, two of which were positively identified as 3,4-dichloroaniline
and N-(3,4-dichlorophenyl)glucosylamine (Still, 1968).
Photolytic. Photoproducts reported from the sunlight irradiation of propanil (200 mg/L)
in distilled water were 3′-hydroxy-4′-chloropropionanilide, 3′-chloro-4′-hydroxypropionanilide, 3′,4′-dihydroxypropionanilide, 3′-chloropropionanilide, 4′-chloropropionanilide,
propionanilide, 3,4-dichloroaniline, 3-chloroaniline, propionic acid, propionamide,
3,3′,4,4′-tetrachloroazobenzene and a dark polymeric humic substance. The photolysis
products resulted from the reductive dechlorination, replacement of chlorine substituents
by hydroxyl groups, formation of propionamide, hydrolysis of the amide group and
azobenzene formation (Moilanen and Crosby, 1972). Tanaka et al. (1985) studied the
photolysis of propanil (100 mg/L) in aqueous solution using UV light (λ = 300 nm) or
sunlight. After 26 days of exposure to sunlight, propanil degraded forming a trichlorinated
biphenyl product (<1% yield) and hydrogen chloride (Tanaka et al., 1985).
Chemical/Physical. Hydrolyzes in acidic and alkaline media to propionic acid (Worthing and Hance, 1991) and 3,4-dichloroaniline (Sittig, 1985; Worthing and Hance, 1991).
The half-life of propanil in a 0.50 N sodium hydroxide solution at 20°C was determined
to be 6.6 days (El-Dib and Aly, 1976). | [storage]
Store at -20°C | [Pesticide Type]
Herbicide |
| Safety Data | Back Directory | [Symbol(GHS) ]
 
GHS07,GHS09 | [Signal word ]
Warning | [Hazard statements ]
H302-H400 | [Precautionary statements ]
P264-P270-P273-P301+P312-P391-P501 | [Hazard Codes ]
Xn;N,N,Xn | [Risk Statements ]
22-50 | [Safety Statements ]
2-22-61 | [RIDADR ]
UN 3077 9/PG 3 | [WGK Germany ]
3 | [RTECS ]
UE4900000 | [HazardClass ]
9 | [PackingGroup ]
III | [HS Code ]
29242990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral
Aquatic Acute 1 | [Safety Profile]
Poison by ingestion.
Moderately toxic by an unspecified route.
Mildly toxic by skin contact. Mutation data
reported. When heated to decomposition it
emits very toxic fumes of Cl and NOx. | [Hazardous Substances Data]
709-98-8(Hazardous Substances Data) | [Toxicity]
LD50 orally in rats: 1384 mg/kg (Bailey, White) |
| Questions And Answer | Back Directory | [Description]
Propanil (3,4-dichloropropionanilide) is an acetanilide post-emergency herbicide with no residual effect. It can be prepared by reaction of 3,4-dichloroaniline with propionic acid in the presence of thionyl chloride. Propanil is in toxicity class II - moderately toxic, due to its potential to irritate eyes and skin.
Propanil functionalizes by the inhibition of RNA/protein synthesis and the inhibition of anthocyanin. Propanil is used to against numerous grasses and broad-leaved weeds in rice (mainly), potatoes, and wheat. It is typically applied aerially.
| [References]
[1] S. M. Richards, G. Y. H. McClure, T. L. Lavy, J. D. Mattice, R. J. Keller, J. Gandy (2001) Propanil (3,4-Dichloropropionanilide) Particulate Concentrations Within and Near the Residences of Families Living Adjacent to Aerially Sprayed Rice Fields, Arch. Environ. Contam. Toxicol. 41, 112–116
[2] Michael A. Kamrin (1997) Pesticide Profiles: Toxicity, Environmental Impact, and Fate
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
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