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Propineb

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Identification
Molecular formula
C10H18N2O4
CAS number
18691-97-9
IUPAC name
[2-(carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate
State
State

At room temperature, Propineb is in a solid state. It exists as a powder that is often formulated into a suspension concentrate or wettable powder for agricultural purposes.

Melting point (Celsius)
107.00
Melting point (Kelvin)
380.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
265.36g/mol
Molar mass
265.3610g/mol
Density
1.6000g/cm3
Appearence

Propineb appears as a white to greyish-white powder with no characteristic odor. The solid is usually supplied in granulated form to reduce dustiness for handling safety.

Comment on solubility

Solubility of [2-(carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate

The solubility of [2-(carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate can be influenced by several factors, including its molecular structure, polarity, and the presence of functional groups.

Typically, the solubility of a compound can be assessed based on:

  • Polarity: Compounds with polar functional groups tend to be more soluble in polar solvents (e.g., water), whereas non-polar compounds are usually soluble in non-polar solvents (e.g., organic solvents).
  • Hydrogen bonding: The presence of carbamate functional groups in this compound suggests that hydrogen bonding may occur, potentially enhancing solubility in water and other protic solvents.
  • Molecular size: Larger molecules can sometimes hinder solubility due to steric hindrance, which may limit interaction with solvent molecules.

In summary, while the exact solubility values for [2-(carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate will depend on experimental conditions, it can generally be anticipated that:

  • It may exhibit moderate solubility in polar solvents due to its carbamate groups.
  • Solubility could also depend on temperature and the specific solvent used.

To explore its solubility further, empirical testing in various solvents is recommended, as the structure suggests it can interact favorably with polar solvents through hydrogen bonding and dipole-dipole interactions.

Interesting facts

Interesting Facts about [2-(Carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate

[2-(Carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate is a fascinating compound that exhibits unique chemical properties and potential applications. Here are some intriguing aspects of this compound:

  • Functional Groups: This compound contains multiple functional groups, including a carbamate moiety, which is known for its versatility in organic chemistry. Carbamates are often utilized in the synthesis of pharmaceuticals and pesticides.
  • Application in Drug Development: Due to its structural characteristics, [2-(Carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate may play a role in medicinal chemistry. Compounds with carbamate groups can enhance bioavailability and improve the pharmacokinetic profiles of drug candidates.
  • Synthetic Versatility: The presence of various substituents on the carbon chain allows for synthetic modifications, making this compound a valuable intermediate in producing other chemical entities.
  • Biological Significance: Research has shown that carbamate derivatives can exhibit biological activity. This compound may serve as a lead structure in developing new therapeutic agents, expanding the range of treatments available for various diseases.

As you can see, the study of [2-(Carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate opens doors to many exciting possibilities in both chemical synthesis and applications in drug design:

  • “The beauty of chemistry lies in the stories that every compound tells through its functionality.”
  • Understanding the nuances of such compounds contributes significantly to advancing modern science!

In summary, this compound's intriguing structural features and potential applications in diverse fields underscore the importance of ongoing research in organic and medicinal chemistry.

Synonyms
TYBAMATE
Tibamato
Solacen
Tibamate
Tibamax
Tybatran
Benvil
Depran
Effisax
Idalene
Nospan
Reposan
Solacin
4268-36-4
W 713
Tybamatum
Tybamatum [INN-Latin]
Tibamato [INN-Spanish]
2-Methyl-2-propyltrimethylene butylcarbamate carbamate
N-Butyl-2-methyl-2-propyl-1,3-propanediol dicarbamate
NSC 172126
2-(Hydroxymethyl)-2-methylpentyl butylcarbamate carbamate
HSDB 3410
2-Methyl-2-propyl-1,3-propanediol butylcarbamate carbamate
EINECS 224-254-9
Carbamic acid, ester with 2-(hydroxymethyl)-2-methylpentyl butylcarbamate
Solacen (TN)
Carbamic acid, butyl-, 2-(((aminocarbonyl)oxy)methyl)-2-methylpentyl ester
NSC-172126
BRN 1970468
Tybamate [USAN:INN:BAN:NF]
3875LLL8M8
TYBAMATE [HSDB]
TYBAMATE [USAN]
Carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester carbamate (ester)
N-n-Butyl-2-methyl-2-propyl-1,3-propanediol dicarbamate
TYBAMATE [INN]
TYBAMATE [MI]
NSC172126
1,3-Propanediol, 2-methyl-2-propyl-, butylcarbamate carbamate
TYBAMATE [WHO-DD]
Carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester, carbamate
Carbamic acid, ester with 2-methyl-2-propyl-1,3-propanediol butylcarbamate
Carbamic acid, butyl-, ester with 2-(hydroxymethyl)-2-methylpentyl carbamate
DTXSID7023728
W-713
Butylcarbamic acid 2-(((aminocarbonyl)oxy)methyl)-2-methylpentyl ester
Carbamate of 2-(hydroxymethyl)-2-methylpentyl ester of butylcarbamic acid
Tybamatum (INN-Latin)
Tibamato (INN-Spanish)
Carbamic acid, butyl-, 2-[[(aminocarbonyl)oxy]methyl]-2-methylpentyl ester
BUTYLCARBAMIC ACID 2-
DTXCID503728
Carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester carbamate (ester) (8CI)
224-254-9
[2-(carbamoyloxymethyl)-2-methylpentyl] N-butylcarbamate
2-(Hydroxymethyl)-2-(methylpentyl) butylcarbamate carbamate
Carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester carbamate
UNII-3875LLL8M8
Tybamate (USAN/INN)
SCHEMBL78046
CHEMBL2104816
CHEBI:135133
WLN: ZVO1X3&1&1OVM4
Carbamic acid,3-propanediol butylcarbamate
NS00031223
D06260
1, 2-methyl-2-propyl-, butylcarbamate carbamate
Q7859691
2-[(carbamoyloxy)methyl]-2-methylpentyl butylcarbamate
[2-(carbamoyloxymethyl)-2-methyl-pentyl] N-butylcarbamate
Carbamic acid, 2-(hydroxymethyl)-2-methylpentyl ester carbamate
1, 3-Propanediol, 2-methyl-2-propyl-, butylcarbamate carbamate
Carbamic acid, ester with 2-(hydroxymethyl)-2-methylpentyl carbamate
Carbamic acid, ester with 2-methyl-2-propyl-1, 3-propanediol butylcarbamate
Carbamic acid, butyl-, {2-[[(aminocarbonyl)oxy]methyl]-2-methylpentyl} ester