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Aldicarb

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Identification
Molecular formula
C7H14N2O2S
CAS number
116-06-3
IUPAC name
[(2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate
State
State

At room temperature, Aldicarb is in a solid state.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
435.00
Boiling point (Kelvin)
708.15
General information
Molecular weight
190.27g/mol
Molar mass
190.2670g/mol
Density
1.1958g/cm3
Appearence

Aldicarb appears as a colorless crystalline solid. Its appearance can also be described as a white powder in its pure form. As a pesticide, it might be distributed in granulated forms mixed with inert materials.

Comment on solubility

Solubility of [(2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate

The solubility of the compound [(2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate (C7H14N2O2S) can be characterized by several factors, given its unique structure and components:

  • Polarity: This compound contains a mixture of polar and nonpolar groups, which may influence its solubility in various solvents.
  • Hydrogen bonding: The presence of the carbamate functional group allows for potential hydrogen bonding with solvents such as water, suggesting some degree of solubility.
  • Medium solubility: While it may exhibit solubility in organic solvents (e.g., ethanol or acetone), it may show limited solubility in water due to its hydrophobic alkyl groups.

In general, the solubility of this compound is expected to be moderate, being more soluble in organic media compared to aqueous solutions. Factors such as temperature and pH can further affect its solubility characteristics.

Overall, understanding the solubility profile of [(2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate is crucial for its applications in chemical formulations and reactions.

Interesting facts

Interesting Facts about [(2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate

[ (2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate, while not as well-known as many other chemical compounds, has garnered attention due to its unique structure and potential applications. Here are some fascinating aspects of this compound:

  • Structural Composition: The compound features a complex arrangement that includes a carbamate functionality. This characteristic makes it interesting for studying the reactivity of nitrogen-containing organic compounds.
  • Potential Applications: Carbamates are often used in agriculture as pesticides. The unique branch of the sulfonyl group in this compound indicates that it may possess specific properties that can enhance pest resistant qualities.
  • Synthesis and Chemistry: Synthesizing carbamates can be an exciting challenge in the laboratory. The method often involves combining alcohols with isocyanates, offering students an excellent opportunity to practice organic synthesis techniques.
  • Biological Relevance: Carbamate compounds can interact with enzymes and neurotransmitter systems. This makes them of interest in pharmacology and toxicology, particularly in their ability to affect cholinergic activity.
  • Environmental Impact: The application of carbamate pesticides has raised discussions about their environmental persistence and impacts on non-target organisms. Understanding their breakdown and ecological footprint is vital for sustainable practices.

In the world of chemistry, the exploration of compounds like [(2-methyl-2-methylsulfanyl-propylidene)amino] N-methylcarbamate not only broadens our knowledge of organic chemistry but also aids in the development of safer and more effective agricultural practices. As students and researchers dive deeper, they continue to uncover the myriad possibilities held within this intriguing compound.

Synonyms
aldicarb
Temik
116-06-3
Aldicarb [ISO]
Carbamyl
Sulfone aldoxycarb
Aldicarbe [French]
Aldicarbe
Temik G10
Caswell No. 011A
Temik 10 G
TEMIK G
Union carbide 21149
2-Methyl-2-(methylthio)propionaldehyde O-(methylcarbamoyl)oxime
RCRA waste number P070
CCRIS 17
Union carbide UC-21149
ENT-27,093
UNII-8V071SH05P
UC-21149
HSDB 1510
UC-21,149
OMS-771
8V071SH05P
NCI-C08640
ALDICARB [HSDB]
ALDICARB [IARC]
ALDICARB [MI]
EINECS 204-123-2
ENT 27093
RCRA waste no. P070
EPA Pesticide Chemical Code 098301
NSC 379586
AI3-27093
CHEBI:2555
DTXSID0039223
NSC-379586
ALDICARB (IARC)
2-Methyl-2-(methylthio)propanal O-[(methylamino)carbonyl]oxime
2-Metil-2-tiometil-propionaldeid-O-(N-metil-carbamoil)-ossima
2-Metil-2-tiometil-propionaldeid-O-(N-metil-carbamoil)-ossima [Italian]
ALDICARBE (FRENCH)
2-Methyl-2-methylthio-propionaldehyd-O-(N-methyl-carbamoyl)-oxim [German]
Carbamic acid, methyl-, O-((2-methyl-2-(methylthio)propylidene)amino) deriv.
Aldecarb
Temic
2-METHYL-2-(METHYLTHIO)PROPANAL O-((METHYLAMINO)CARBONYL)OXIME
Propionaldehyde, 2-methyl-2-(methylthio)-, O-(methylcarbamoyl)oxime
Temik G 10
2-Methyl-2-methylthio-propionaldehyd-O-(N-methyl-carbamoyl)-oxim
DTXCID1039
ENT 27,093
UC 21149
[(2-methyl-2-methylsulfanylpropylidene)amino] N-methylcarbamate
(E)-(2-methyl-2-(methylsulfanyl)propylidene)amino N-methylcarbamate
(E)-[2-methyl-2-(methylsulfanyl)propylidene]amino N-methylcarbamate
2-METHYL-2-METHYLTHIO-PROPIONALDEHYD-O-(N-METHYL-CARBAMOYL)-OXIM (GERMAN)
2-METIL-2-TIOMETIL-PROPIONALDEID-O-(N-METIL-CARBAMOIL)-OSSIMA (ITALIAN)
Temik 10G
TEMIK TSK
Spectrum_001913
SpecPlus_000544
Spectrum3_000852
Spectrum4_000692
Union carbide UC21149
Pesticide Code: 098301
KBioGR_001183
KBioSS_002455
DivK1c_006640
2-Methyl-2-methylthio-propionaldehyd-O-(N-methyl-carbamoyl)-oxime
OMS771
CHEMBL3182309
KBio1_001584
KBio2_002448
KBio2_005016
KBio2_007584
KBio3_001963
OMS 771
QGLZXHRNAYXIBU-UHFFFAOYSA-N
FA29243
UN 2757
Aldicarb 100 microg/mL in Acetonitrile
2Metil2tiometilpropionaldeidO(Nmetilcarbamoil)ossima
2Methyl2methylthiopropionaldehydO(Nmethylcarbamoyl)oxim
Q63088093
2Methyl2(methylthio)propanal, O((methylamino)carbonyl)oxime
2Methyl2(methylthio)propionaldehyde O(methylcarbamoyl)oxime
N-methylcarbamoyloxime,2-methylthio-2-methylpropionaldehyde
O-(Methylcarbamoyl)-2-methyl-2-(methylthio)propionaldehyd-oxime
Propanal, 2methyl2(methylthio), O((methylamino)carbonyl)oxime
2-methyl-2-(methylthio) propionaldehyde O-(methylcarbamoyl) oxime
O-(Methylcarbamoyl)-2-methyl-2-(methylthio)propionaldehyde-oxime
2-METHYL-2-(METHYLTHIO)PROPANAL, O-((METHYLAMINO)CARBONYL) OXIME
2-METHYL-2-(METHYLTHIO)PROPANAL, O-((METHYLAMINO)CARBONYL))OXIME
Carbamic acid, methyl, O((2methyl2(methylthio)propylidene)amino) deriv.
CARBAMIC ACID, METHYL-, O-((2-METHYL-2-(METHYLTHIO)PROPYLIDENE) AMINO) DERIVATIVE
PROPANAL, 2-METHYL-2-(METHYLTHIO)-, O-((METHYLAMINO)CARBONYL) OXIME
PROPIONALDEHYDE, 2-METHYL-2-(METHYLTHIO)-, O-(METHYL-CARBAMOYL)OXIME
204-123-2