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Ephedrine

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Identification
Molecular formula
C10H15NO
CAS number
299-42-3
IUPAC name
2-(methylamino)-1-phenyl-propan-1-ol
State
State

At room temperature, ephedrine exists as a solid.

Melting point (Celsius)
34.00
Melting point (Kelvin)
307.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
165.24g/mol
Molar mass
165.2360g/mol
Density
1.1434g/cm3
Appearence

Ephedrine appears as a white, crystalline powder.

Comment on solubility

Solubility of 2-(methylamino)-1-phenyl-propan-1-ol (C10H15NO)

The solubility characteristics of 2-(methylamino)-1-phenyl-propan-1-ol, a compound with the formula C10H15NO, can be intriguing due to its molecular structure, which includes both a polar amine group and an aromatic ring.

Key Aspects of Solubility:

  • Solvent Compatibility: This compound is generally expected to be soluble in polar solvents such as water and alcohols, primarily due to the presence of the -NH group, which can form hydrogen bonds with water molecules.
  • Hydrophobic Interactions: The phenyl group, being hydrophobic, may lead to decreased solubility in purely aqueous environments. Therefore, its solubility may be higher in organic solvents like methanol or ethanol compared to water.
  • Temperature Influence: As with many organic compounds, temperature may significantly impact solubility. Increasing the temperature can enhance solubility by promoting greater molecular motion.

In conclusion, while 2-(methylamino)-1-phenyl-propan-1-ol exhibits the potential for good solubility in certain solvents, the balance between its polar and non-polar characteristics plays a pivotal role. As a general rule of thumb, "like dissolves like," indicating that understanding the interplay of these functional groups is essential for predicting its behavior in different solvents.

Interesting facts

Interesting Facts about 2-(Methylamino)-1-phenyl-propan-1-ol

2-(Methylamino)-1-phenyl-propan-1-ol, often abbreviated as MAP, is a fascinating compound that finds its place in various fields of research due to its unique characteristics. Here are some interesting facts about this compound:

  • Pharmaceutical Relevance: MAP has been studied for its potential therapeutic effects, particularly in the context of mental health and neurological disorders.
  • Chemical Structure: The compound features a methylamino group, which contributes to its pharmacological activity, making it a subject of interest in medicinal chemistry.
  • Synthetic Pathways: Various synthetic routes have been developed for the production of MAP, showcasing the compound's versatility in organic chemistry.
  • Potential Applications: Research indicates that MAP may have applications in drug development for conditions such as depression and anxiety, though further studies are necessary to fully understand its efficacy and safety.
  • Toxicity Assessments: As with many compounds that exhibit biological activity, understanding the toxicity profile of MAP is crucial in ensuring its safe use in clinical settings.

In the words of a prominent chemist, “Every molecule tells a story.” The story of MAP is still unfolding, and ongoing research continues to reveal its potential and challenges in the realm of medicinal chemistry. Whether in the laboratory or in clinical trials, this compound reminds us of the intricate relationship between chemistry and health!

Synonyms
53214-57-6
racephedrine
2-(methylamino)-1-phenylpropan-1-ol
2-(Methylamino)-1-phenyl-1-propanol
1-EPHEDRINE
Benzenemethanol, .alpha.-[1-(methylamino)ethyl]-
1-Phenyl-2-methylaminopropanol
Benzyl alcohol, .alpha.-(1-methylaminoethyl)-
Ephedrine,(+)
Ephedrine, (-)-
Pseudoephedrine, (-)
1-.alpha.-(1-Methylaminoethyl)-benzyl alcohol
Ephedrital
Ephedrosan
Ephedrotal
Ephendronal
Racefedrina
Efedrin
Ephedsol
Ephoxamin
Kratedyn
Manadrin
Vencipon
Zephrol
Nasol
Racephedrine hydrochloride
NSC8971
Benzenemethanol, [R-(R*,S*)]-
WLN: QYR & Y1 & M1
l-.alpha.-(1-Methylaminoethyl)benzyl alcohol
Ephedrine,(-)
(-)-.alpha.-(1-Methylaminoethyl)benzyl alcohol
.alpha.-Hydroxy-.beta.-methyl amine propylbenzene
(1R,2S)-(-)-ephedrine
NSC 165609
NSC170951
1-alpha-(1-Methylaminoethyl)-benzyl alcohol
1-Hydroxy-2-methylamino-1-phenylpropane
BENZYL ALCOHOL, alpha-(1-METHYLAMINOETHYL)-
Spectrum2_001309
Spectrum3_000563
Spectrum4_000497
Spectrum5_001106
SCHEMBL4369
Benzenemethanol, alpha-(1-(methylamino)ethyl)-
1R, 2S (-)-Ephedrine
Oprea1_287330
BSPBio_001946
Ephedrine, (.+/-.)-
KBioGR_001013
WLN: QYR&Y1&M1
DivK1c_000181
DivK1c_000461
SPBio_001377
Benzenemethanol, .alpha.-[1-(methylamino)ethyl]-, [S-(R*,R*)]-
CHEMBL279157
BDBM86284
KBio1_000181
KBio1_000461
KBio3_001446
DTXSID70858959
NINDS_000181
NINDS_000461
HMS3370H05
CAS_5032
STR02792
BBL010298
NSC165609
PDSP1_000168
PDSP1_001106
PDSP2_000167
PDSP2_001090
STK367993
AKOS005445214
NSC-165609
IDI1_000181
IDI1_000461
2-(Methylamino)-1-phenyl-1-propanol #
NCGC00015408-02
NCGC00015408-05
DA-05155
Benzenemethanol,a-[1-(methylamino)ethyl]-
SBI-0051503.P003
CAS_24221-86-1
NS00098609
C22822
AB01563268_01
L000968
BRD-A54236247-003-02-7
BRD-A54236247-003-03-5
BRD-A54236247-003-04-3
Benzenemethanol, .alpha.-[1-(methylamino)ethyl]-, (R*,S*)-(.+/-.)-