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Isopropyl ethyl methylcarbamate

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Identification
Molecular formula
C8H15NO2
CAS number
4170-30-3
IUPAC name
(1-ethyl-1-methyl-propyl) carbamate
State
State

At room temperature, the compound is in a liquid state.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
294.50
Boiling point (Kelvin)
567.65
General information
Molecular weight
145.20g/mol
Molar mass
145.2010g/mol
Density
1.0100g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid with a faint characteristic odor. It is an ester of carbamic acid.

Comment on solubility

Solubility of (1-ethyl-1-methyl-propyl) carbamate

(1-ethyl-1-methyl-propyl) carbamate exhibits interesting characteristics regarding its solubility, primarily dependent on its **polarity** and **functional groups**. The presence of the carbamate functional group enhances its potential for solubility in various solvents.

Solubility in Water

As a member of the carbamate family, (1-ethyl-1-methyl-propyl) carbamate has some degree of solubility in water due to hydrogen bonding capabilities. Here are some key points:

  • Moderate solubility: It is expected to dissolve moderately in water, influenced by temperature.
  • Hydrogen bonding: The hydroxyl group enhances its interaction with water molecules.

Solubility in Organic Solvents

This compound is likely to show a higher solubility in organic solvents due to its alkyl groups' hydrophobic nature. The following characteristics can be noted:

  • High solubility: It is likely soluble in non-polar and moderately polar organic solvents.
  • Compatibility: Given its alkyl chains, it may be compatible with solvents like ethanol, acetone, or ether.

In summary, the solubility of (1-ethyl-1-methyl-propyl) carbamate is marked by its dual nature: it has a reasonable solubility in water while favoring organic solvents due to its molecular structure. Understanding this solubility behavior is crucial for its applications in various chemical processes.

Interesting facts

Interesting Facts About (1-ethyl-1-methyl-propyl) Carbamate

(1-ethyl-1-methyl-propyl) carbamate, often simply referred to as a carbamate derivative, is a fascinating compound that plays a significant role in various fields of chemistry, particularly in agrochemistry and medicinal chemistry. Here are some interesting insights:

  • Chemical Classification: This compound belongs to the carbamate family, which are esters of carbamic acid. Carbamates are widely recognized for their applications as herbicides, insecticides, and pesticides in agriculture.
  • Biological Activity: Many carbamates, including this one, exhibit interesting biological properties. They can act as enzyme inhibitors, particularly of the acetylcholinesterase enzyme, which is crucial in nerve function.
  • Industrial Relevance: Due to their stability and efficacy, carbamates are used in several industrial applications, including the manufacture of plastics, coatings, and pharmaceuticals.
  • Synthetic Routes: The synthesis of (1-ethyl-1-methyl-propyl) carbamate can involve various methods, including the reaction of isocyanates with alcohols. This presents exciting opportunities to explore green chemistry methods for production.
  • Environmental Considerations: The environmental impact of carbamate compounds is a topic of ongoing research. Understanding their biodegradation pathways is crucial for mitigating ecological risks.

With its diverse applications and remarkable properties, (1-ethyl-1-methyl-propyl) carbamate serves as a compelling subject of study, highlighting the intricate connections between chemistry, biology, and environmental science. As scientists continue to explore its potential benefits and drawbacks, it remains a vital compound within both industrial and academic circles.

Synonyms
Emylcamate
78-28-4
Emilcamato
Emylcamat
3-methylpentan-3-yl carbamate
Nuncital
Psicoplegil
Restetal
Stratran
Striatan
Striatran
Statran
1-Ethyl-1-methylpropyl carbamate
tert-Hexanol carbamate
3-Methyl-3-pentanol carbamate
KABI-925
Kabi-295
tert-Hexyl carbamate
Diethyl methyl carbinol urethan
MK-250
Methyl diethyl carbinol urethan
Emylcamatum
91 JD
JD-91
3-Pentanol, 3-methyl-, carbamate
Emylcamate [INN:BAN]
Carbamic acid, tert-hexyl ester
Emylcamatum [INN-Latin]
Emilcamato [INN-Spanish]
KABI 925
Stratan
NSC 169882
CARBAMIC ACID, 1-ETHYL-1-METHYLPROPYL ESTER
terc.Hexylester kyseliny karbaminove
EINECS 201-101-4
UNII-KCJ747D3R4
Emylcamate (INN)
NSC-169882
BRN 1755436
KCJ747D3R4
terc.Hexylester kyseliny karbaminove [Czech]
EMYLCAMATE [MI]
EMYLCAMATE [INN]
EMYLCAMATE [WHO-DD]
DTXSID40228645
4-03-00-00058 (Beilstein Handbook Reference)
3-Pentanol, carbamate
Emylcamatum (INN-Latin)
Emilcamato (INN-Spanish)
WLN: ZVOX2&2&1
KAB 1925
3-Pentanol, 3-methyl-, carbamate (8CI)
SCHEMBL387718
CHEMBL2104208
DTXCID90151136
N05BC03
CHEBI:134769
AAA07828
NSC169882
NSC169917
AKOS006273433
DB13572
NSC-169917
DA-63179
HY-121340
CS-0081492
NS00037982
D07317
EN300-212804
3-Pentanol, 3-methyl-, carbamate (8CI)(9CI)
Q378997
Z1198155508
201-101-4