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3-Methyl-3-pentyn-1-ol

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Identification
Molecular formula
C6H10O
CAS number
77-75-8
IUPAC name
3-methylpent-1-yn-3-ol
State
State
The compound is a liquid at room temperature, characterized by its clarity and lack of color.
Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
142.30
Boiling point (Kelvin)
415.45
General information
Molecular weight
98.16g/mol
Molar mass
98.1610g/mol
Density
0.8620g/cm3
Appearence

3-Methyl-3-pentyn-1-ol typically appears as a clear, colorless liquid. It may have a slightly oily consistency. Its appearance can sometimes be described as a viscous liquid, indicating its higher molecular weight relative to simple alcohols.

Comment on solubility

Solubility of 3-methylpent-1-yn-3-ol

3-methylpent-1-yn-3-ol, a compound with the formula C6H10O, exhibits interesting solubility characteristics that are noteworthy for both practical applications and theoretical studies. The solubility of this compound can be influenced by various factors such as:

  • Hydrophilicity vs. Hydrophobicity: Due to the presence of the hydroxyl (-OH) group, 3-methylpent-1-yn-3-ol demonstrates some level of hydrophilic properties, allowing it to dissolve well in polar solvents such as water to a certain degree.
  • Solvent Interaction: This compound tends to be more soluble in organic solvents like alcohols or ethers. Common organic solvents in which it might dissolve include methanol, ethanol, and acetone.
  • Temperature Influence: An increase in temperature generally enhances solubility; thus, heating the solvent may increase the amount of 3-methylpent-1-yn-3-ol that can be dissolved.

It is important to note that while 3-methylpent-1-yn-3-ol can be soluble in water, it is often more significantly soluble in organic media. Therefore, when considering its application, the choice of solvent is crucial.

Overall, while 3-methylpent-1-yn-3-ol possesses moderate solubility characteristics, understanding its solubility profile is essential for maximizing its utility in various chemical processes.

Interesting facts

Interesting Facts About 3-Methylpent-1-yn-3-ol

3-Methylpent-1-yn-3-ol is a unique compound that falls under the category of alcohols due to the presence of a hydroxyl (-OH) functional group, alongside an alkyne (a carbon-carbon triple bond). This combination adds an intriguing twist to its chemistry and potential applications. Below are some notable characteristics:

  • Structural Complexity: The compound features a five-carbon backbone that is substituted with a methyl group and a hydroxyl group, giving it diverse reactivity and the ability to participate in various chemical reactions.
  • Reactivity: The presence of both the alkyne and alcohol functional groups allows for a range of reactions, including hydration, oxidation, and substitution reactions. This makes it an interesting compound for synthetic organic chemistry.
  • Synthesis: 3-Methylpent-1-yn-3-ol can be synthesized using different methods, such as nucleophilic additions or through the modification of existing alcohols and alkynes, showcasing the versatility of organic synthesis techniques.
  • Applications: Although specific applications for this compound may not be widely known, compounds featuring both alcohol and alkyne functionalities are often used as intermediates in the production of pharmaceuticals and agrochemicals.
  • Chemistry in Nature: Understanding compounds like 3-methylpent-1-yn-3-ol sheds light on natural products that exhibit similar structural characteristics. Many phytochemicals belonging to the alkyne family exhibit biological activity, highlighting potential applications in medicinal chemistry.

In essence, 3-methylpent-1-yn-3-ol illustrates the intriguing intersection of alcohol and alkyne chemistry. As a compound that presents many routes for exploration, it is a prime candidate for research in both synthetic advancements and natural product studies.

Synonyms
3-Methyl-1-pentyn-3-ol
77-75-8
Methylpentynol
Meparfynol
3-Methylpent-1-yn-3-ol
Atemorin
Methylparafynol
Seral
Allotropal
Melpintol
Methylpentinol
Metilparafinolo
Metilpentinolo
Noxokratin
Sedapercut
1-Pentyn-3-ol, 3-methyl-
Aniphor
Apridol
Citodorm
Dormalest
Dormidin
Dormigen
Dormiphen
Dormison
Dormocit
Dormosan
Formison
Hexofen
Imnudorm
Insomnol
Macarol
Mecarol
Mepentil
Miramel
Oblevil
Oblivon
Olvadon
Pentadorm
Pentinol
Pentyrest
Perlopal
Riposon
Sintyal
Somnesin
Sonnormon
Comesa
Dalgol
Olosot
Methylpentynolum
Anti-stress
N-Oblivon
2-Ethynyl-2-butanol
2-Butanol, 2-ethynyl-
3-Methylpentyn-3-ol
Olfine P
Ethinylmethylethylcarbinol
Methylethylethynylcarbinol
Metilpentinol
Pentydorm
Methylethylacetylenylcarbinol
3-Methylpentin-3-ol
Ethyl ethynyl methyl carbinol
3-Metil-pentin-3-ol
Dorison
Hesofen
Pentydrom
UTIL
Methylpentynol [INN]
2-Ethinyl butanol-2
3-Methyl-pentin-(1)-ol-(3)
NSC-28797
BDH
Methylpentanol
m-Pentynol
B017BC5B1N
2-Ethinylbutanol
DTXSID5021756
MEPARFYLON
Methylpentynol (INN)
3-Methyl-1-pentynol
NCGC00166025-01
.alpha.-Ethyl-.alpha.-methylpropargyl alcohol
2-Ethinylbutanol-2
WLN: QX2&1&1UU1
Metilpentinolo [DCIT]
3-Methyl-1-pentyn-2-ol
Methylpentynol [INN:BAN]
Metilpentinol [INN-Spanish]
Methylpentynolum [INN-Latin]
3-Metil-pentin-3-ol [Italian]
(+-)-3-Methylpent-1-yn-3-ol
EINECS 201-055-5
NSC 28797
3-methyl-1-pentyne-3-ol
BRN 0969340
UNII-B017BC5B1N
alpha-Ethyl-alpha-methylpropargyl alcohol
3-Methyl-pentin-(1)-ol-(3) [German]
Methylpentinolum
AI3-14502
AI3-37931
Atemorin (TN)
MFCD00004479
MEPARFYNOL [MI]
Ethynylethylmethylcarbinol
3-Methyl-1-pentin-3-ol
EC 201-055-5
4-01-00-02242 (Beilstein Handbook Reference)
METHYLPENTYNOL [MART.]
3-hydroxy-3-methyl-1-pentyne
CHEMBL501613
DTXCID401756
NSC975
METHYLPENTYNOL [WHO-DD]
Pent-1-yne-3-ol, 3-methyl-
NSC-975
CHEBI:134752
HMS3264A21
3-Methyl-1-pentyn-3-ol, 98%
ALBB-031801
NSC28797
Tox21_112294
AKOS009158777
CCG-214047
DB13733
FM35088
(.+/-.)-3-Methylpent-1-yn-3-ol
CAS-77-75-8
3-Methyl-1-pentyn-3-ol Methyl pentynol
NCGC00166025-02
Ethyl ethynyl methyl carbinol, Meparfynol
LS-11587
(+/-)-3-METHYLPENT-1-YN-3-OL
M0396
NS00009052
D07332
D91328
EN300-104662
AB01563255_01
Q412090
SR-01000944285
SR-01000944285-1
BRD-A11662333-001-01-7
BRD-A11662333-001-03-3
Z1251192957