Skip to main content

Isopropyl methanesulfonate

ADVERTISEMENT
Identification
Molecular formula
C4H10O3S
CAS number
1919-31-9
IUPAC name
isopropyl methanesulfonate
State
State

At room temperature, isopropyl methanesulfonate is in a liquid state.

Melting point (Celsius)
-61.00
Melting point (Kelvin)
212.00
Boiling point (Celsius)
142.00
Boiling point (Kelvin)
415.00
General information
Molecular weight
140.19g/mol
Molar mass
140.1850g/mol
Density
1.0910g/cm3
Appearence

Isopropyl methanesulfonate is typically a colorless liquid.

Comment on solubility

Solubility of Isopropyl Methanesulfonate

Isopropyl methanesulfonate, with the chemical formula (CH3)2CHOCH3SO3, exhibits notable characteristics regarding its solubility that are worth highlighting:

  • Highly Soluble in Polar Solvents: This compound is known for its excellent solubility in polar solvents such as water and methanol. The polar nature of the methanesulfonate group contributes significantly to this solubility.
  • Limited Solubility in Non-Polar Solvents: Conversely, isopropyl methanesulfonate shows much lower solubility in non-polar solvents. This behavior is typical for compounds featuring charged or highly polar functional groups.
  • Influence of Temperature: The solubility may also vary with temperature, where increased temperatures can lead to enhanced solubility, a common phenomenon observed in many chemical compounds.
  • Applications in Organic Synthesis: Due to its favorable solubility properties, isopropyl methanesulfonate is often utilized in organic synthesis and as a reactive intermediate.

In summary, the solubility of isopropyl methanesulfonate underscores its versatility in chemical applications, emphasizing the importance of solvent choice when working with this compound. As noted, "like dissolves like", and understanding the solubility characteristics is crucial for effective usage in laboratory settings.

Interesting facts

Interesting Facts about Isopropyl Methanesulfonate

Isopropyl methanesulfonate is a notable compound in the field of organic chemistry, frequently utilized in various chemical reactions and applications. Here are some essential insights about this fascinating compound:

  • Reactivity: This compound is regarded for its ability to act as an electrophilic reagent, which makes it a significant player in nucleophilic substitution reactions.
  • Synthesis: It can be synthesized through the reaction of isopropanol with methanesulfonyl chloride, showcasing a classic method of formation that highlights its chemical versatility.
  • Applications: Isopropyl methanesulfonate is prevalent in several fields including:
    • Pharmaceuticals
    • Agricultural chemicals
    • Intermediates in organic synthesis
  • Mechanism of Action: The compound often participates in processes that involve the formation of carbon-sulfur bonds, making it valuable in developing various chemical entities.
  • Environmental Impact: Understanding the degradation and environmental implications of isopropyl methanesulfonate is crucial for assessing its long-term sustainability and responsible usage in industrial applications.

In the words of renowned chemist Robert H. Grubbs, "The molecular transformations that occur in our laboratories today set the stage for the innovations of tomorrow." Isopropyl methanesulfonate exemplifies this notion, bridging theoretical chemistry and practical applications.

Given its diverse applications and significant role in chemical reactions, isopropyl methanesulfonate remains an intriguing topic for students and chemists alike as they explore the dynamic world of organic compounds.

Synonyms
ISOPROPYL METHANESULFONATE
926-06-7
Isopropyl mesylate
Isopropylmethanesulfonate
Isopropyl methanesulphonate
Isopropyl methane sulphonate
Methanesulfonic acid, 1-methylethyl ester
2-Propyl methanesulphonate
Isopropyl methane sulfonate
Methanesulfonic acid, isopropyl ester
CCRIS 1103
HSDB 5519
UNII-T0K2TXY26B
EINECS 213-132-0
BRN 1750157
DTXSID8031497
AI3-62142
Isopropyl methanesulfate
DTXCID6011497
ISOPROPYL METHANESULFONATE [HSDB]
methanesulfonic acid 1-methylethyl ester
2Propyl methanesulfonate
2Propyl methanesulphonate
Methanesulfonic acid, 1methylethyl ester
2-propyl methanesulfonate
4-04-00-00013 (beilstein handbook reference)
swwhcqcmvcpleq-uhfffaoysa-n
propan-2-yl methanesulfonate
MFCD00047802
T0K2TXY26B
Methanesulfonic acid 1-methylethyl ester; Methanesulfonic acid, isopropyl ester (6CI,7CI,8CI); 2-Propyl methanesulfonate; Isopropyl mesylate; Isopropyl methanesulfonate; Isopropyl methanesulphonate
Methanesulfonate Isopropyl
MLS002174258
SCHEMBL331716
CHEMBL1320187
Isopropyl methanesulfonate, 95%
HMS3039L15
AAA92606
Methanesulfonic Acid Isopropyl Ester
Tox21_200855
BBL102511
STL556314
AKOS015852416
CS-W022766
DS-5051
NCGC00090722-01
NCGC00090722-02
NCGC00258409-01
CAS-926-06-7
SMR001261428
SY052242
DB-057314
I0914
NS00039475
EN300-298241
O11833
Q27289509