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Vitamin B6

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Identification
Molecular formula
C8H11NO2
CAS number
65-23-6
IUPAC name
4-(aminomethyl)-5-(hydroxymethyl)-2-methyl-pyridin-3-ol
State
State

The compound is typically in a solid state at room temperature. It is stable under standard conditions and should be stored in a cool, dry place away from direct sunlight.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.00
Boiling point (Celsius)
333.00
Boiling point (Kelvin)
606.00
General information
Molecular weight
169.18g/mol
Molar mass
169.1780g/mol
Density
1.3965g/cm3
Appearence

The compound appears as a white crystalline powder. It is often colorless or might have a slightly yellow hue depending on purity. It is stable under normal conditions but may degrade when exposed to light.

Comment on solubility

Solubility of 4-(aminomethyl)-5-(hydroxymethyl)-2-methyl-pyridin-3-ol (C8H11NO2)

The solubility of 4-(aminomethyl)-5-(hydroxymethyl)-2-methyl-pyridin-3-ol is influenced by several factors due to its chemical structure and functional groups. This compound features both amino and hydroxymethyl groups, which can engage in hydrogen bonding. As a result, we can expect the following:

  • Hydrophilic behavior: The presence of the hydroxymethyl (-CH2OH) and amino (-NH2) groups often enhances solubility in polar solvents such as water.
  • Solubility in organic solvents: Although it has polar characteristics, solubility may vary in different polar organic solvents.
  • Temperature influence: Increasing temperature typically increases solubility for many compounds; hence, this might also apply for C8H11NO2.

In conclusion, the solubility of 4-(aminomethyl)-5-(hydroxymethyl)-2-methyl-pyridin-3-ol is likely to be reasonable in water, associated with its ability to form hydrogen bonds. However, precise solubility data would require experimental determination for a clear characterization.

Interesting facts

Interesting Facts about 4-(Aminomethyl)-5-(hydroxymethyl)-2-methyl-pyridin-3-ol

This compound is a fascinating example of a pyridine derivative, showcasing a unique combination of functional groups that gives it distinctive properties. As a chemist, it's intriguing to explore its potential applications and biological significance.

Key Characteristics:

  • Contains both aminomethyl and hydroxymethyl groups, which can contribute to its reactivity and solubility in various solvents.
  • The structure includes a methyl group at the 2-position, which may influence its biological activity and interactions.
  • Part of the pyridine family, this compound benefits from the aromatic properties of the ring, making it a valuable starting point for further chemical synthesis.

Moreover, compounds like this one are often researched for their potential pharmaceutical applications. They can be studied for their activity as:

  • Enzyme inhibitors in various metabolic pathways.
  • Antioxidants that play a role in combating oxidative stress in biological systems.
  • Neuroprotective agents, contributing to treatment strategies for neurodegenerative diseases.

Furthermore, the presence of hydroxymethyl and amine functionalities emphasizes the importance of hydrogen bonding, which is crucial in biological interactions. Understanding the chemical behavior of this compound can help pave the way for novel drugs and therapies.

As a final thought, the exploration of such a complex molecule opens up discussions around structure-activity relationships, an essential concept in medicinal chemistry. One might say, "In chemistry, the beauty lies not only in understanding the compounds but also in their potential to transform lives."

Synonyms
pyridoxamine
85-87-0
Pyridoxylamine
4-(AMINOMETHYL)-5-(HYDROXYMETHYL)-2-METHYLPYRIDIN-3-OL
3-Pyridinemethanol, 4-(aminomethyl)-5-hydroxy-6-methyl-
CHEBI:16410
EINECS 201-640-5
UNII-6466NM3W93
4-(Aminomethyl)-5-(hydroxymethyl)-2-methyl-3-pyridinol
PYRIDOXAMINE [MI]
6466NM3W93
NCIStruc1_000457
NCIStruc2_000537
Oprea1_400404
CBDivE_013510
PYRIDOXAMINE [WHO-DD]
DTXSID6046929
NCI21278
NCGC00013273
NCI60_001792
NSC21278
EU-0067145
NSC-21278
C00534
PXM
2-methyl-4-aminomethyl-5-hydroxymethyl-3-Pyridinol
3-Pyridinol, 2-methyl-4-aminomethyl-5-hydroxymethyl-
4-(aminomethyl)-5-hydroxy-6-methyl-3-Pyridinemethanol
PXL
EN300-6481455
MFCD00464815
nchembio.93-comp3
LS-187048
LS-187660
bmse000130
SCHEMBL30408
4-aminomethyl-5-hydroxy-6-methyl-3-pyridinemethanol
CHEMBL593019
DTXCID4026929
BDBM626197
ALBB-005914
HY-B1745
CCG-38056
STK503617
AKOS000264716
DB11673
GS-3241
NCGC00013273-02
NCGC00096392-01
DB-231724
CS-0013764
NS00014913
EN300-254254
F82068
SR-01000392002
Q2541149
SR-01000392002-1
BRD-K96669468-300-01-1
4-(aminomethyl)-3-hydroxy-2-methyl-5-pyridinemethanol
48DD06CB-7B30-4F04-8D74-6F84BDBF5AA9
4-(Aminomethyl)-5-(hydroxymethyl)-2-methyl-3-pyridinol #
2-methylpyridin-3-ol-5-(hydroxymethyl)-2-methylpyridin-3-ol
4-(azaniumylmethyl)-5-(hydroxymethyl)-2-methylpyridin-3-olate
4-(Aminomethyl)-5-(hydroxymethyl)-2-methylpyridin-3-ol dihydrochloride hydrate
201-640-5