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Promecarb

HCID 17516
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
2631-37-0
Standard SMILES
CNC(=O)Oc1cc(C)cc(C(C)C)c1
InChIKey
DTAPQAJKAFRNJB-UHFFFAOYSA-N
Molecular formula
C12H17NO2
Average molar mass
207.27 g/mol
Monoisotopic mass
207.12592879

Overview

Almost odorless, colorless crystalline solid. Used as a non-systemic contact insecticide. Not for sale or use in the USA. (EPA, 1998)

Names & identifiers

Preferred name
Promecarb
IUPAC
(3-methyl-5-propan-2-ylphenyl) N-methylcarbamate
English name
PROMECARB
Molecular formula
C12H17NO2
Molecular weight
207.27

Names & synonyms

PROMECARB2631-37-0CarbamultMinacidePromecarbem-Cym-5-yl methylcarbamateMorton EP-316Schering 346153-Isopropyl-5-methylphenyl methylcarbamateNor-AmSch 34615Union carbide UC-9880
Show more names
ITCt-32ep316oms716Sn-316uc9880sn34615UC 9880
OMS 7165-Methyl-m-cumenyl methylcarbamateENT 27,300-aCaswell No. 271C3-Methyl-5-isopropylphenyl methylcarbamateEP 316Carbamic acid, methyl-, m-cym-5-yl ester3-Isopropyl-5-methylphenyl N-methylcarbamate

Database identifiers

CAS
2631-37-0
PubChem CID
17516
DTXSID
DTXSID4037617
ChEMBL
CHEMBL1076537
ChEBI
CHEBI:82096
UNII
1QRP20775S
EC Number
220-113-0
Nikkaji
J3.034A

Properties

Computed structural properties

XLogP
3.1
Topological polar surface area
38.3 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
2
Rotatable bonds
3
Heavy atoms
15
Formal charge
0
Complexity
216

Experimental & physicochemical properties

SpringerMaterials PropertiesFusion temperature
Pesticides · 4 items

Insecticides

Active substance -> EU Pesticides database: Not approved

Pesticides -> Carbamate Insecticides

Pesticide (Promecarb) -> USDA PDB

LogP · 2 items

log Kow= 3.10 (measured)

3.1

OdorALMOST ODORLESS
Color/FormCOLORLESS CRYSTALLINE SOLID
Solubility · 2 items

SOL IN POLAR ORG SOLVENTS

91 MG/L IN WATER @ ROOM TEMP; 100-200 G/L IN CARBON TETRACHLORIDE, XYLENE; 200-400G/L IN CYCLOHEXANOL, CYCLOHEXANONE, 2-PROPANOL, METHANOL; 400-600 G/L IN ACETONE, DIMETHYLFORMAMIDE, 1,2-DICHLOROETHANE

CorrosivityNon-corrosive
Boiling Point · 3 items

243 °F at 0.01 mmHg (EPA, 1998)

117 °C AT 0.1 MM HG

345 °C @760 [mm Hg]

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Danger

H301: Toxic if swallowed [Danger Acute toxicity, oral]

P264, P270, P273, P301+P316, P321, P330, P391, P405, and P501 (click each P-code to see the statement)

Danger

H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral]

P264, P270, P273, P301+P316, P321, P330, P391, P405, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 2 items

2002/2076

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - Phenol, 3-methyl-5-(1-methylethyl)-, methyl carbamate: Environment tier I assessment
DOT LabelPoison
Fire Hazards · 1 item

(Non-Specific -- Carbamate Pesticide, Solid, n.o.s.) Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Hydrolyzed by alkalis. Stable. No changes observed on storage for 140 hours at122F. (EPA, 1998)

Health HazardsPromecarb is highly toxic by ingestion and is absorbed through the intact skin. It is a reversible cholinesterase inhibitor and its effects are related to action on the nervous sysem. (EPA, 1998)
Hazards Summary · 1 item

A cholinesterase inhibitor; Most of the aromatic carbamate insecticides have low dermal absorption; Rats receiving 5 mg orally every day for 1.5 years showed no adverse effects; Most rats die after doses of 50 mg/kg/day for 3 months; [HSDB] A reversible cholinesterase inhibitor; Can be absorbed through skin; [CAMEO] May cause irritation; Can be absorbed through skin; [MSDSonline] See CARBAMATE INSECTICIDES.

Chemistry & industry

Pharmacology

Mechanism of Action · 2 items

Carbamylation of acetylcholinesterase produces accumulation of acetylcholine and the picture of muscarine and nicotinic poisoning. /Carbamate pesticides/

Cholinesterase inhibitor.

Metabolism/Metabolites · 5 items

Promecarb was rapidly metabolized and eliminated when administered orally to rats. By 96 hours after administration, over 90% had been recovered from the urine and feces, mainly the former. Promecarb equivalent radioactivity in the tissues did not exceed 0.02 ppm.

(5-(14)C)Promecarb was administered orally to male Sprague Dawley rats. Within 4 days, about 88% of the dose was eliminated in the urine. In addition to isothymol, there were unidentified metabolites. Hydrolysis with glucuronidase indicated the conjugation of isothymol with glucuronic acid. Other conjugates present were not identified.

Promecarb was applied to soil and then corn seedlings were planted. Analyses of stem and leaves of the plants indicated the presence of isothymol and four unidentified metabolites as early as 15 days after application.

Spontaneous hydrolysis of the carbamate-cholinesterase complex occurs in vivo, leading to the disappearance of clinical effects within 24 hr. /Carbamate pesticides/

The carbamates are hydrolyzed enzymatically by the liver; degradation products are excreted by the kidneys and the liver. (L793)

Absorption, Distribution and Excretion · 3 items

... /CARBAMATE INSECTICIDES/ ARE RAPIDLY METABOLIZED, 80% OF DOSE BEING ELIMINATED IN URINE, MAINLY AS SULFATE OR GLUCURONIDE CONJUGATE, WITHIN 24 HR; 0.5 TO 1.5% IS FOUND IN FECES, 0.1 TO 1.0% IN THE MILK. /CARBAMATES/

In order to learn why cholinesterase remains inhibited longer in workers exposedto promecarb than in those exposed to propoxur, dogs were injected im or iv with approximately equitoxic doses of the compounds. It required 3 full days for cholinesterase activity to return to normal in a dog that received promecarb intramuscularly at a rate of 60 mg/kg, but recovery of cholinesterase activity was rapid after doses of propoxur sufficient to cause convulsions and marked ataxia. However, inhibition of cholinesterase activity was transient following intravenous administration of promecarb. It was concluded that prolonged inhibition of cholinesterase activity in days following im injection was the result of slow, continuing absorption and that, by extension, prolonged inhibition in workers has the same cause.

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Melting Point · 2 items

189 to 190 °F (EPA, 1998)

87-87.5 °C

Vapor Pressure · 4 items

3e-05 mmHg at 77 °F (EPA, 1998)

0.00003 [mmHg]

3X10-5 mm Hg @ 25 °C

0.00003 [mm Hg] @25 °C

Physical Description · 2 items

Almost odorless, colorless crystalline solid. Used as a non-systemic contact insecticide. Not for sale or use in the USA. (EPA, 1998)

Colorless solid; [Hawley]

Stability/Shelf Life · 2 items

No change at 50 °C for 140 hr, half life @ pH 7, 310 hr & @ pH 9, 5.7 hr.

Hydrolyzed in alkalies

Physicochemical properties

Melting point
87.5 ℃ · 87.5℃
Boiling point
117 ℃ · 117℃ (10-12 Torr)
Density
1.0681 · 1.0681 (rough estimate)
refractive index
1.522 · 1.5220 (estimate)
storage temp.
0 · 0-6°C
solubility
Chloroform (Slightly), Methanol (Slightly)
pka
12.37 · 12.37±0.46(Predicted)
form
Crystalline
color
White to Off-White
Water Solubility
92 mg/L · 92mg/L(room temperature)
Merck
13 · 13,7875
BRN
2111695 · 2111695
Henry's Law Constant
1.1 · 1.1×102 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
InChI
1S/C12H17NO2/c1-8(2)10-5-9(3)6-11(7-10)15-12(14)13-4/h5-8H,1-4H3,(H,13,14)
InChIKey
DTAPQAJKAFRNJB-UHFFFAOYSA-N
SMILES
CNC(=O)Oc1cc(C)cc(c1)C(C)C
CAS DataBase Reference
2631 · 2631-37-0(CAS DataBase Reference)
EWG's Food Scores
1 · 1
FDA UNII
1 QRP20775S · 1QRP20775S
EPA Substance Registry System
Promecarb (2631-37-0)
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
6 · GHS06,GHS09
Signal word
Danger
Hazard statements
301 · H301-H410
Precautionary statements
264 · P264-P270-P273-P301+P310-P330-P391-P405-P501
Hazard Codes
T,N
Risk Statements
25 · 25-50/53
Safety Statements
24 · 24-37-45-60-61
RIDADR
2757 · 2757
WGK Germany
3 · 3
RTECS
8050000 · FB8050000
HazardClass
6.1 · 6.1(a)
PackingGroup
II
Storage Class
6.1 A · 6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
Hazard Classifications
2 OralAcute · Acute Tox. 2 OralAcute Tox. 3 DermalAquatic Acute 1Aquatic Chronic 1
Hazardous Substances Data
2631 · 2631-37-0(Hazardous Substances Data)
Toxicity
50 in · LD50 in mice, rats (mg/kg): 39.5, 60 orally (Miyao)
Reactive GroupCarbamates
Reactivity Profile · 1 item

PROMECARB is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.

DOT Hazard Classification · 2 items

Promecarb

Marine pollutant

Air and Water ReactionsNo rapid reaction with air. No rapid reaction with water.
Hazard Classes and Categories · 4 items

Acute Tox. 3 (97.6%)

Acute toxicity - category 3

Acute toxicity (Oral) - Category 2

Acute Tox. 3 *

Shipment Methods and Regulations · 3 items

No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./

The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials.

The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article.

Safety & protection

Fire Fighting · 1 item

(Non-Specific -- Carbamate Pesticide, Solid, n.o.s.) Stay upwind; keep out of low areas. Move container from fire area if you can do it without risk. Fight fire from maximum distance. Dike fire control water for later disposal; do not scatter the material. Wear positive pressure breathing apparatus and special protective clothing.

First AidNote: Promecarb is a cholinesterase inhibitor.
Exposure Control and Personal Protection · 1 item

Biological Exposure Indices (BEI) [ACGIH] - Acetylcholinesterase activity in red blood cells = 70% of individual's baseline; Butylcholinesterase activity in serum or plasma = 60% of individual's baseline; Sample at end of shift; [TLVs and BEIs]

Nonfire Spill Response · 1 item

(Non-Specific -- Carbamate Pesticide, Solid, n.o.s.) Keep unnecessary people away; isolate hazard areas and deny entry. Stay upwind and keep out of low areas. Do not touch spilled material or breathe the dusts, vapors, or fumes from burning materials. Use water spray to reduce vapors. Do not handle broken packages without protective equipment. Wash away any material that may have contacted the body with soap and water. Take up small spills with sand or other noncombustible absorbent material and place in containers for later disposal.

Disposal MethodsHydrolysis: Promecarb should be treated with alkali and then buried. Recommendable methods: Incineration & landfill.
Preventive MeasuresCarefully wash with soap & water any parts or the skin contracted with promecarb.
Isolation and EvacuationExcerpt from ERG Guide 151 [Substances - Toxic (Non-Combustible)]:
Protective Action Criteria (PAC) · 3 items

0.11 [mg/m3]

1.2 [mg/m3]

7.1 [mg/m3]

Personal Protective Equipment (PPE) · 2 items

For emergency situations, wear a positive pressure, pressure-demand, full facepiece self-contained breathing apparatus (SCBA) or pressure- demand supplied air respirator with escape SCBA and a fully-encapsulating, chemical resistant suit. (EPA, 1998)

Wear protective clothing when working with undiluted preparation.

Toxicology

Treatment · 1 item

If the compound has been ingested, rapid gastric lavage should be performed using 5% sodium bicarbonate. For skin contact, the skin should be washed with soap and water. If the compound has entered the eyes, they should be washed with large quantities of isotonic saline or water. In serious cases, atropine and/or pralidoxime should be administered. Anti-cholinergic drugs work to counteract the effects of excess acetylcholine and reactivate AChE. Atropine can be used as an antidote in conjunction with pralidoxime or other pyridinium oximes (such as trimedoxime or obidoxime), though the use of '-oximes' has been found to be of no benefit, or possibly harmful, in at least two meta-analyses. Atropine is a muscarinic antagonist, and thus blocks the action of acetylcholine peripherally.

Health Effects · 1 item

Acute exposure to cholinesterase inhibitors can cause a cholinergic crisis characterized by severe nausea/vomiting, salivation, sweating, bradycardia, hypotension, collapse, and convulsions. Increasing muscle weakness is a possibility and may result in death if respiratory muscles are involved. Accumulation of ACh at motor nerves causes overstimulation of nicotinic expression at the neuromuscular junction. When this occurs symptoms such as muscle weakness, fatigue, muscle cramps, fasciculation, and paralysis can be seen. When there is an accumulation of ACh at autonomic ganglia this causes overstimulation of nicotinic expression in the sympathetic system. Symptoms associated with this are hypertension, and hypoglycemia. Overstimulation of nicotinic acetylcholine receptors in the central nervous system, due to accumulation of ACh, results in anxiety, headache, convulsions, ataxia, depression of respiration and circulation, tremor, general weakness, and potentially coma. When there is expression of muscarinic overstimulation due to excess acetylcholine at muscarinic acetylcholine receptors symptoms of visual disturbances, tightness in chest, wheezing due to bronchoconstriction, increased bronchial secretions, increased salivation, lacrimation, sweating, peristalsis, and urination can occur. Chronically high (>10 years) exposure leads to neuropsychological consequences including disturbances in perception and visuo-motor processing (A15321).

Ecotoxicity Values · 3 items

LC50 Trout 0.3 mg/l/96 hr /Conditions of bioassay not specified/

LC50 Carp 4.3 mg/l/96 hr /Conditions of bioassay not specified/

LD50 Duck oral 3.5 mg/kg

Environmental Fate · 3 items

TERRESTRIAL FATE: The N-methylcarbamate pesticides (of which promecarb is a member) are generally biodegradable and of low soil persistence(1). Chemical degradation of promecarb in moist soil is expected to proceed via hydrolysis. The aqueous hydrolysis half-life has been estimated to be 1.2 days at 25 °C and pH 7; the hydrolysis rate is expected to increase under alkaline conditions, but decrease with acidity in soil. Promecarb is expected to have low to moderate soil mobility which suggests that some leaching may be possible. Leaching in neutral and alkaline soils may not be significant, however, due to concurrent hydrolysis(SRC).

AQUATIC FATE: Hydrolysis appears to be an important degradation process for promecarb in water. The aqueous hydrolysis half-life has been estimated to be 1.2 days at 25 °C and pH 7(1); the hydrolysis rate is expected to increase under alkaline conditions, but may decrease significantly in acidic in natural waters.

ATMOSPHERIC FATE: Based upon a vapor pressure of 0.00003 mm Hg at 25 °C(1), promecarb can be expected to exist in both the gas phase and particulate phase in the ambient atmosphere(2,SRC). Gas phase promecarb is expected to degrade rapidly in air by reaction with photochemically produced hydroxyl radicals; the half-life for this reaction in an average atmosphere has been estimated to be about 5 hr. Particulate phase promecarb may be physically removed from air via wet and dry deposition(SRC).

Food Survey ValuesAnalysis by the US Food and Drug Administration of 7,893 samples of domestic and imported fruits and 165 ready to eat fruit composites of the Total Diet Study for fiscal years 1970-1976 found promecarb in only one large fruit sample(1).
Adverse EffectsOther Poison - Carbamate
Exposure RoutesInhalation (L793) ; oral (L793); dermal (L793)
Toxicity Summary · 1 item

Promecarb is a cholinesterase or acetylcholinesterase (AChE) inhibitor. Carbamates form unstable complexes with chlolinesterases by carbamoylation of the active sites of the enzymes. This inhibition is reversible. A cholinesterase inhibitor suppresses the action of acetylcholine esterase. Because of its essential function, chemicals that interfere with the action of acetylcholine esterase are potent neurotoxins, causing excessive salivation and eye-watering in low doses. Headache, salivation, nausea, vomiting, abdominal pain and diarrhea are often prominent at higher levels of exposure. Acetylcholine esterase breaks down the neurotransmitter acetylcholine, which is released at nerve and muscle junctions, in order to allow the muscle or organ to relax. The result of acetylcholine esterase inhibition is that acetylcholine builds up and continues to act so that any nerve impulses are continually transmitted and muscle contractions do not stop.

Signs and Symptoms · 1 item

As with organophosphates, the signs and symptoms are based on excessive cholinergic stimulation. Unlike organophosphate poisoning, carbamate poisonings tend to be of shorter duration because the inhibition of nervous tissue acetylcholinesterase is reversible, and carbamates are more rapidly metabolized. Muscle weakness, dizziness, sweating and slight body discomfort are commonly reported early symptoms. Headache, salivation, nausea, vomiting, abdominal pain and diarrhea are often prominent at higher levels of exposure. Contraction of the pupils with blurred vision, incoordination, muscle twitching and slurred speech have been reported. (L795)

Soil Adsorption/Mobility · 1 item

Utilizing soil thin-layer chromatography, the Rf value of promecarb in Hagerstown silty clay loam soil was measured to be 0.34 which is suggestive of low to moderate soil mobility(1). Based upon a water solubility of 91 ppm at 25 °C(2) and a measured log Kow of 3.10(3), the Koc value for promecarb can be estimated to range from 365 to 1240 from various regression-derived equations(4,SRC). These estimated Koc values also indicate low to medium soil mobility(5).

Human Toxicity Excerpts · 4 items

Symptomatology: 1. Nausea, vomiting, abdominal cramps, diarrhea & excessive salivation ... sweating. 2. Lassitude & weakness. 3. Rhinorrhea and sensation of tightness in chest may occur with inhalation exposure. 4. Blurring or dimness of vision. Miosis ... tearing, ciliary muscle spasm, loss of accommodation and ocular pain. None of these ... signs ... is dependable for diagnosis. Mydriasis may be seen ... . 5. Loss of muscle coordination, slurring of speech, fasciculation & twitching of muscles. 6. Difficulty in breathing, excessive secretions of saliva and of resp tract mucus, oronasal frothing, cyanosis, pulmonary rales & rhonchi, and hypertension. 7. ... Jerky movements, incontinence, convulsions and coma. 8. Death ... due to resp arrest of central origin, paralysis of resp muscles, intense bronchoconstriction or all three. /Carbaryl/

... MOST OF AROMATIC CARBAMATE ESTER INSECTICIDES HAVE LOW DERMAL TOXICITIES. /CARBAMATES/

Promecarb was tried on a village scale at the WHO Insecticide Testing Unit in Nigeria, in 1965. Its residual action against adult mosquitos was found very effective. Three spraymen spent 3 days spraying empty houses and then 3 more days spraying an inhabited village. They were under constant medical supervision. There were no complaints, and clinical examination failed to reveal any signs. All the 90 inhabitants of the sprayed village were examined clinically at least once within the fortnight after spraying. The only findings were discrete skin eruptions in two young men. These eruptions, of an obvious contact dermatitis type, caused moderate itching that was relieved by calamine lotion; they disappeared completely in 5 to 6 days. ... The plasma cholinesterase levels were studied among the spraymen and residents by the electrometric, spectrophotometric, and Acholest methods; a significant depression of activity was demonstrated by all three. The plasma cholinesterase activity of the three spraymen was measured daily. All showed depressions from the first day onward. During 3 days of consecutive spraying, the level of activity went steadily down in two of the three spraymen. On the last day of the operation, the plasma cholinesterase activity of one sprayman was about 40.% of its original level when measured by the spectrophotometric and Acholest methods. Three to four days after the end of exposure, plasma cholinesterase activity among the spraymen had not quite returned to the level measured before exposure, but it was normal in 5 days. Among the residents, there was a decrease of plasma cholinesterase activity to about 50% of the prespraying level a week after the end of the spraying operations One month later, there was a general rise, but the plasma cholinesterase levels were still far below the original values.

When tested for malaria control, promecarb caused cholinesterase inhibition amoung both sprayers and villagers but no signs or symptoms in either except for contact dermatitis in two male villagers.

Artificial Pollution SourcesPromecarb is used as a non-systemic contact insecticide against lepidopterous pests and leaf miners of fruits(1). Insecticidal applications of promecarb release the compound directly into the environment(SRC).

Safety data

wgk
3
rtecs
FB8050000
ridadr
2757
Toxicity
LD50 in mice, rats (mg/kg): 39.5, 60 orally (Miyao)
risk_code
25-50/53
Signal word
Danger
Symbol(GHS)
GHS06,GHS09
hazard_code
T,N
safety_code
24-37-45-60-61
hazard_class
6.1(a)
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
packing_group
II
Hazard statements
H301-H410
Hazard Classifications
Acute Tox. 2 OralAcute Tox. 3 DermalAquatic Acute 1Aquatic Chronic 1
Precautionary statements
P264-P270-P273-P301+P310-P330-P391-P405-P501
Hazardous Substances Data
2631-37-0(Hazardous Substances Data)

Penetration of the blood-brain barrier by the carbamates is insignificant; for this reason, fewer CNS symptoms occur. /Carbamate pesticides/

Uses & manufacturing

Uses · 6 items

Used as contact insecticide (outside the US); Likely discontinued for pesticide use worldwide; [HSDB]

Not sold or used in the US; [CAMEO]

Farming (Pesticides) [Category: Industry]

INSECTICIDE (NON-US USE ONLY)

Promecarb is used as a non-systemic contact insecticide against lepidopterous pests and leaf miners of fruits.

For Colorado potato beetle, ... corn rootworm.

Methods of Manufacturing · 2 items

REACTION OF 3-ISOPROPYL-5-METHYLPHENOL & METHYL ISOCYANATE

/PROMECARB IS/ MADE BY REACTION OF 5-ISOPROPYL-M-CRESOL WITH METHYL ISOCYANATE ... .

Formulations/PreparationsEMULSIFIABLE CONCENTRATE (200 G ACTIVE INGREDIENT/L); WETTABLE POWDER (375 AND 500 G/KG).
General Manufacturing Information · 4 items

The WHO Recommended Classification of Pesticides by Hazard identifies Promecarb (technical grade) as an active ingredient believed to be obsolete or discontinued for use as a pesticide.

WEST GERMAN PATENT 1,156,272; BRITISH PATENT 916,707

PROMECARB IS A NON-SYSTEMIC CONTACT INSECTICIDE EFFECTIVE AGAINST COLEOPTEROUS PESTS SUCH AS POST-EMBRYONIC STAGES OF LEPTINOTARSA DECEMLINEATA @ 450 G ACTIVE INGREDIENT/HECTARE, AGAINST LEPIDOPTEROUS PESTS AND LEAF MINERS OF FRUIT @ 50-100 G/L.

INCOMPATIBLE WITH ALKALINE PREPARATIONS.

Applications · 3 items

UsesPromecarb is a carbamate pesticide.

UsesInsecticide.

General DescriptionAlmost odorless, colorless crystalline solid. Used as a non-systemic contact insecticide. Not for sale or use in the USA.

Suppliers30 total

阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
广州佳途科技股份有限公司81960175-877 18933936954 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
南通合润生物科技有限公司18362409333 · [email protected]
上海毕楷科技有限公司18516304666 · [email protected]
四川库利南科技有限公司400-1166-196 18981987031 · [email protected]
艾科试剂4008-755-333 18080918076 · [email protected]
Clearsynth Labs Limited+91-22-26355700 · [email protected]
南京生利德生物科技有限公司025-57798810 18652991625 · [email protected]
天津阿尔塔科技有限公司022-65378550-8551 · [email protected]
天津荣燊化工有限公司18317763565; 18317763565 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
陕西缔都医药化工有限公司029-029-81120477 17792793610 · [email protected]
南通市苏北化工原料有限公司0513-85290972 18762756250 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
南京罗迈美生物科技有限公司[email protected]
山东小野化学股份有限公司0539-6362799 20)
上海百舜生物科技有限公司021-37581181 · [email protected]
厦门盈融达化工有限公司+86-0592-6210733 · [email protected]
深圳聚合生化科技有限公司+86-400-002-6226 13028896684 · [email protected]
Aladdin Scientific[email protected]
爆牛贸易重庆有限公司+86-023-6139-8061 +86-86-13650506873 · [email protected]
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.+8618950047208 · [email protected]
SUZHOU SENFEIDA CHEMICAL CO.,LTD+86-0512-83500002 +86-15195660023 · [email protected]
上海宝杨宝欣生物科技有限公司021-56698539 19921169802 · [email protected]
上海安谱实验科技股份有限公司18502138905 · [email protected]
上海杰股生物科技有限公司021-51698675 · [email protected]
亚索试剂400-873-6778 18660992876 · [email protected]
南通众合化工新材料有限公司0513-85666561 15950816326 · [email protected]

Additional notes

DefinitionChEBI: Promecarb is an alkylbenzene.