ChemicalBook > CAS DataBase List > Pirimicarb

Pirimicarb

Product Name
Pirimicarb
CAS No.
23103-98-2
Chemical Name
Pirimicarb
Synonyms
Primicarb;Demo;Abol;pp062;Rapid;APHOX;TOMBA;PILLY;PP 062;Fernos
CBNumber
CB8481649
Molecular Formula
C11H18N4O2
Formula Weight
238.29
MOL File
23103-98-2.mol
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Pirimicarb Property

Melting point:
90.5°C
Boiling point:
380.88°C (rough estimate)
Density 
1.1387 (rough estimate)
vapor pressure 
2.1 x 10-3 Pa (30 °C)
refractive index 
1.6081 (estimate)
Flash point:
>100 °C
storage temp. 
APPROX 4°C
solubility 
Acetone (Slightly), Chloroform (Slightly), Methanol (Slightly)
pka
4.34 (weak base)
Water Solubility 
3060 mg l-1
Merck 
13,7579
BRN 
663442
LogP
1.700
CAS DataBase Reference
23103-98-2(CAS DataBase Reference)
NIST Chemistry Reference
Pirimicarb(23103-98-2)
EPA Substance Registry System
Pirimicarb (23103-98-2)
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Safety

Hazard Codes 
T;N,N,T,Xn,F
Risk Statements 
25-50/53-36-20/21/22-11
Safety Statements 
22-37-45-60-61-36-26-16-36/37
RIDADR 
UN 2811
WGK Germany 
3
RTECS 
EZ9100000
HazardClass 
6.1(b)
PackingGroup 
III
Hazardous Substances Data
23103-98-2(Hazardous Substances Data)
Toxicity
LD50 orally in female rats: 147 (mg/kg) (Baranyovits, Ghosh)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H317May cause an allergic skin reaction

H351Suspected of causing cancer

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P202Do not handle until all safety precautions have been read and understood.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
45627
Product name
Pirimicarb
Purity
PESTANAL
Packaging
250mg
Price
$31.7
Updated
2024/03/01
Sigma-Aldrich
Product number
44719
Product name
Pirimicarb
Purity
reference material
Packaging
100mg
Price
$148
Updated
2022/05/15
Usbiological
Product number
462698
Product name
Pirimicarb
Packaging
250mg
Price
$305
Updated
2021/12/16
TRC
Product number
P508768
Product name
Pirimicarb
Packaging
250mg
Price
$50
Updated
2021/12/16
TRC
Product number
P508768
Product name
Pirimicarb
Packaging
1g
Price
$120
Updated
2021/12/16
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Pirimicarb Chemical Properties,Usage,Production

Description

Pirimicarb is a colorless solid that is moderately soluble in water, acetone, ethanol, xylene, and chloroform.
Pirimicarb is produced by reaction of 2-dimethylamino- 5,6-dimethyl-4-pyrimidone with dimethylcarbamic acid chloride in the presence of a base or phosgene and dimethylamine. Pirimicarb is a systemic, selective aphicide used largely on grain crops, but also on ornamentals, cotton, fruit, and in greenhouses.

Chemical Properties

Colorless crystalline solid. Odorless. Commercial product may be available as a liquid

Uses

Insecticide.

Uses

Pirimicarb is a systemic insecticide with contact, stomach and respiratory action. It is a selective aphicide used in cereals, fruit, ornamentals, strawberries, potatoes, sugar beet, fodder beet, cotton, oilseed rape, tobacco and glasshouse crops.

Definition

ChEBI: An aminopyrimidine that is N,N,4,5-tetramethylpyrimidin-2-amine substituted by a (dimethylcarbamoyl)oxy group at position 4.

Health Hazard

Highly toxic insecticide by oral and possibly other routes of entry; cholinesteraseinhibitor; median oral lethal doses in experimental animals ranged at 100–150 mg/kg;toxic symptoms include excessive salivation,lacrimation, slow heartbeat, blurred vision,headache, muscle twitching, tremor and convulsion; gastrointestinal effects include vomiting, nausea, abdominal pain, and diarrhea;severe poisoning can progress to death.
LD50 oral (rat): ~50 mg/kg
LD50 oral (dog): 100 mg/kg.

Agricultural Uses

Insecticide: Originally registered in the U.S. for non-food use on alfalfa grown for seed in selected. Elsewhere it is used on a wide range of cereals, potatoes, fruits, vegetables and other crop.

Trade name

ABOL®; AFICIDA®; APHOX®; FERNOS®; PIRIMIKARB; PIRIMOR®; PP 062®; PYRIMOR®; RAPID®

Potential Exposure

Primicarb is a carbamate (N-methyl) insecticide. Originally registered in the United States for non-food use on alfalfa grown for seed in selected. Elsewhere it is used on a wide range of cereals, potatoes, fruits, vegetables and other crop

Metabolic pathway

The influence on the qualitative photochemical behavior of pirimicarb which leads to the photoproducts N-formylpirimicarb and demethylpirimicarb is modified by the waxes that are extracted from nectarines, oranges, and mandarin oranges. The formation of the photoproducts is hindered by the waxes.

Shipping

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Degradation

Pirimicarb is hydrolysed in alkaline solutions (PM). Sterilised buffer solutions of unlabelled pirimicarb at pH values of 4,7 and 9 were incubated in the dark at 50 °C for 5 days. Samples were taken and analysed by HPLC. No hydrolysis of pirirnicarb was detected. At longer incubation times, some of the N-formyl derivative (2) (see Scheme 1) was produced (PSD, 1995). [14C-pyrimidinyl]Pirimicarb was dissolved in buffer solutions of pH 5,7 or 9 and exposed to natural sunlight (August in southern England) for up to 27 days. Losses of radioactivity by volatilisation were insignificant. After 3 weeks virtually all the pirimicarb was degraded. In neutral and acid solutions the main product was the N-formyl derivative (2). At pH 9 this was unstable. The N-monodemethylpirimicarb (3), aminopirimicarb (4) and the pyrimidinol(5) were also identified and some polar products were formed.
A further study under similar conditions (August 1974) afforded compounds 14 and the pyrimidinol derivatives (5, 6, 7). N,N-Dimethylguanidine (8), N-methylguanidine (9) and guanidine (10) were identified by electrophoretic methods. The guanidines were formed by opening of the pyrimidine ring (PSD, 1995). These pathways are illustrated in Scheme 1.
In other studies in which aqueous solutions or solid samples of pirimicarb were exposed to sunlight or lamps in the laboratory, the products 2, 3, 4 and 5 were also found, the first usually being the major product. Pirisi ef al. (1996) also detected a formylaminodimethylcarbamate (11) whilst Romero et al. (1994) reported that the formaminopyrimidinol (12) was formed via the N-formyl compound (2). [14C-pyrimidinyl]Pirimicarb was applied to a silty-clay loam on a thin-layer plate coated with soil. The plate was exposed under polythene to sunlight in southern England. Pirimicarb was completely degraded over 20 days. The major degradation product was the pyrimidinol (5) formed by hydrolysis of the carbamate ester group. No volatile products were detected (Hill, 1976; PSD, 1995).

Incompatibilities

May react with strong oxidizers such as chlorates, peroxides, and nitrates. May form explosive materials with phosphorus pentachloride.

Waste Disposal

Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using a licensed disposal contractor to an approved landfill. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Incineration with effluent gas scrubbing is recommended. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

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View Lastest Price from Pirimicarb manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Pirimicarb 23103-98-2
Price
US $0.00-0.00/Kg
Min. Order
1KG
Purity
99.0%
Supply Ability
500 tons
Release date
2020-04-26
Shaanxi Dideu Medichem Co. Ltd
Product
Pirimicarb 23103-98-2
Price
US $1.00-0.00/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
600 tons
Release date
2020-04-24
Career Henan Chemical Co
Product
pirimicarb 23103-98-2
Price
US $9.80/KG
Min. Order
1KG
Purity
≥98%
Supply Ability
20 tons
Release date
2020-01-09

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