Skip to main content

Methylhexanamine

ADVERTISEMENT
Identification
Molecular formula
C8H19NO
CAS number
105-41-9
IUPAC name
6-amino-2-methyl-heptan-2-ol
State
State

At room temperature, methylhexanamine is in a liquid state.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
151.00
Boiling point (Kelvin)
424.15
General information
Molecular weight
129.24g/mol
Molar mass
129.2410g/mol
Density
0.8729g/cm3
Appearence

Methylhexanamine appears as a clear, colorless liquid with a mild amine odor. It is typically supplied in a pure form and is sensitive to air and moisture.

Comment on solubility

Solubility of 6-amino-2-methyl-heptan-2-ol (C8H19NO)

6-amino-2-methyl-heptan-2-ol is an organic compound that exhibits interesting solubility characteristics. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of the amino group (-NH2) and hydroxyl group (-OH) leads to increased polarity, which generally enhances solubility in polar solvents like water.
  • Hydrogen bonding: Both the hydroxyl and amino functional groups can participate in hydrogen bonding, which further supports solubility in polar solvents. As stated, “Compounds that can hydrogen bond tend to have better solubility in water.”
  • Hydrophobic interactions: The hydrocarbon part of the molecule may decrease solubility in highly polar solvents, as the non-polar tails have a tendency to seek out non-polar environments.

Considering these factors, it can be said that:

  1. 6-amino-2-methyl-heptan-2-ol is expected to be soluble in water, but its solubility may not be as high compared to smaller, more polar amino alcohols.
  2. In organic solvents, solubility may vary widely, dependent on their polarity. The compound may find better solubility in less polar organic solvents.

Overall, exploring the solubility in various solvents can lead to a deeper understanding of the compound's behavior in different chemical environments!

Interesting facts

Interesting Facts about 6-amino-2-methyl-heptan-2-ol

6-amino-2-methyl-heptan-2-ol is a versatile compound that plays a significant role in various fields, particularly in organic chemistry and medicinal applications. Here are some intriguing aspects of this compound:

  • Amino Alcohol Structure: This compound is classified as an amino alcohol, which means it features both an amino group and a hydroxyl group. This combination allows for unique chemical reactivity and potential biological activity.
  • Synthesis Applications: 6-amino-2-methyl-heptan-2-ol can serve as an intermediate in the synthesis of larger organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Chiral Center: The structure contains a chiral center, making it an interesting subject for studies focused on stereochemistry. Stereoisomers can exhibit different biological activities, so understanding this property is crucial for drug design.
  • Potential Biological Activity: Compounds with amino alcohol functionality often show biological relevance, including potential neuroprotective effects and activity against various diseases. Research is ongoing to explore its full therapeutic potential.
  • Research Significance: This compound represents a small piece of the vast puzzle in organic and medicinal chemistry, illustrating how even seemingly simple molecules can have significant implications for health and industry.

In summary, 6-amino-2-methyl-heptan-2-ol is not just another compound; it embodies the intricate intersection of chemistry and biology, showcasing the importance of such structures in scientific research and practical applications. As scientists continue to explore its properties, the potential for discovering new uses remains promising.

Synonyms
heptaminol
6-amino-2-methylheptan-2-ol
372-66-7
6-Amino-2-methyl-2-heptanol
Corasore
Heptaminolum
Ginkor
2-HEPTANOL, 6-AMINO-2-METHYL-
2-Methyl-2-hydroxy-6-aminoheptane
Heptaminol [INN:BAN]
Heptaminolum [INN-Latin]
EINECS 206-758-0
UNII-3DQS188SY5
Heptaminol (INN)
2-methyl-6-amino-2-heptanol
BRN 1209267
3DQS188SY5
6-hydroxy-6-methyl-2-heptamine
HEPTAMINOL [MI]
2-Amino-6-hydroxy-6-methylheptane
HEPTAMINOL [INN]
RP-2831 hydrochloride
HEPTAMINOL [WHO-DD]
DTXSID4048484
4-04-00-01809 (Beilstein Handbook Reference)
6-METHYL-2-AMINO-6-HEPTANOL
Heptaminol (>85%)
6-HYDROXY-6-METHYL-2-HEPTYLAMINE
6-HYDROXY-6-METHYL-2-AMINOHEPTANE
(5-HYDROXY-1,5-DIMETHYLHEXYL)AMINE
Heptaminolum (INN-Latin)
Ginkor Fort
eptaminolo
Gincor-fort
acAfylline heptaminol
Spectrum_000001
Prestwick0_000015
Prestwick1_000015
Prestwick2_000015
Prestwick3_000015
Spectrum2_001536
Spectrum3_001907
Spectrum4_000167
Spectrum5_001020
6-amino2-methyl-2-heptanol
BSPBio_000049
BSPBio_003474
KBioGR_000653
KBioSS_000341
DivK1c_000924
SCHEMBL152610
SPBio_001352
SPBio_001970
BPBio1_000055
CHEMBL2111076
DTXCID0028458
CHEBI:94362
KBio1_000924
KBio2_000341
KBio2_002909
KBio2_005477
KBio3_002978
C01DX08
NINDS_000924
BDBM50101812
STK664816
AKOS005536007
DB13574
HY-W685943
IDI1_000924
NCGC00178043-01
NCGC00178043-02
1ST11095
6-Amino-2-methyl-2-heptanol, AldrichCPR
6-amino-2-methylheptan-2-ol,hydrochloride
SBI-0051789.P002
AB00053652
CS-0769718
NS00005329
D07158
G73857
AB00053652_04
A874136
Q417921
BRD-A32988684-003-01-2
BRD-A32988684-003-08-7
206-758-0