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Vitamin K3

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Identification
Molecular formula
C11H8O2
CAS number
58-27-5
IUPAC name
2-(12-hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-1,4-benzoquinone
State
State

At room temperature, Vitamin K3 is generally in a solid state, often stored as a powder due to its stability in this form. It maintains its structure and does not sublime or evaporate easily under normal conditions.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.15
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.15
General information
Molecular weight
240.31g/mol
Molar mass
240.3130g/mol
Density
1.6900g/cm3
Appearence

Vitamin K3, also known as menadione, typically appears as a yellow crystalline powder. It is noteworthy for its vibrant color and powdery texture when observed closely. The compound is often utilized in various formulations and applications.

Comment on solubility

Solubility of 2-(12-hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-1,4-benzoquinone (C11H8O2)

The solubility of 2-(12-hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-1,4-benzoquinone is characterized by several significant factors that can influence its behavior in different solvents. Understanding these factors can provide insights into its applications in various chemical processes.

Key Factors Impacting Solubility:

  • Polarity: The presence of hydroxyl groups can enhance solubility in polar solvents like water, whereas nonpolar solvents may be used for better solubility of the overall structural framework.
  • Hydrophobic Interactions: The long hydrocarbon chain may impart hydrophobic characteristics, influencing its solubility in organic solvents.
  • Temperature: Increased temperatures often lead to higher solubility due to enhanced molecular motion.

It is important to note that "solubility" is not a fixed property. Several factors can alter the solubility conditions, including:

  1. Concentration: Higher concentrations of the compound can result in solubility limitations.
  2. Presence of other solutes: Other chemical entities can either enhance or hinder solubility through competitive interactions.

In summary, while C11H8O2 may exhibit variable solubility across different solvents, its solubility behavior is crucial for its utility in chemical applications. Understanding these interactions is essential for predicting its behavior in practical scenarios.

Interesting facts

Interesting Facts about 2-(12-hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-1,4-benzoquinone

This compound showcases a fascinating structure that combines organic chemistry principles with rich biochemical properties. Here are some key points of interest:

  • Structural Complexity: The presence of multiple functional groups, including hydroxyl and quinone structures, contributes to its diverse reactivity.
  • Potential Biological Activity: Compounds similar to this benzoquinone are often investigated for their biological roles, including their potential as antioxidants and in anticancer research.
  • Natural Sources: Quinones like this one are often derived from natural sources such as plants, where they play a role in pigmentation and protection against environmental stresses.
  • Applications in Material Science: The unique properties of this compound make it a candidate for use in materials science, particularly in creating advanced materials with desirable electronic or optical properties.
  • Intriguing Synthesis: Synthesizing such complex molecules can serve as a challenging yet rewarding experience for chemists, often requiring innovative synthetic strategies.

As highlighted in a recent study, "Molecules with intricate functional groups can exhibit unique physical and chemical properties, opening doors for novel applications"—this benzoquinone exemplifies such potential. The presence of multiple methyl substitutions hints at a rich landscape of reactivity and stability, making it an exciting subject for future research and exploration in both organic chemistry and pharmacology.

Synonyms
DOCEBENONE
aa-861
80809-81-0
Docebenona
Docebenonum
AA861
2-(12-hydroxydodeca-5,10-diyn-1-yl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione
Docebenone [USAN:INN]
Docebenonum [INN-Latin]
Docebenona [INN-Spanish]
AA 861
CHEBI:2340
2-(12-Hydroxy-5,10-dodecadiynyl)-3,5,6-trimethyl-p-benzoquinone
A-61589
2,3,5-trimethyl-6-(12-hydroxy-5,10-dodecadiynyl)-1,4-benzoquinone
2XRX3BD53M
DTXSID0045125
DOCEBENONE [INN]
DOCEBENONE [USAN]
DOCEBENONE [MART.]
2-(12-hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-1,4-benzoquinone
2-(12-hydroxydodeca-5,10-diynyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione
2,5-Cyclohexadiene-1,4-dione, 2-(12-hydroxy-5,10-dodecadiynyl)-3,5,6-trimethyl-
MLS000028467
DTXCID8025125
6-(12-hydroxydodeca-5,10-diyn-1-yl)-2,3,5-trimethyl-1,4-benzoquinone
NCGC00015053-05
SMR000058412
2-[12-Hydroxydodeca-5,10-diynyl]-3,5,6-trimethyl-p-benzoquinone
Docebenonum (INN-Latin)
Docebenona (INN-Spanish)
DOCEBENONE (MART.)
2-(12-Hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-p-benzoquinone
2,5-CYCLOHEXADIENE-1,4-DIONE, 2-(12-HYDROXY-5,10-DODECADIYN-1-YL)-3,5,6-TRIMETHYL-
CAS-80809-81-0
UNII-2XRX3BD53M
Docembenone
A 61589
Docebenone (USAN/INN)
Opera_ID_1818
Lopac-A-3711
2,5-Cyclohexadiene-1,4-dione,2-(12-hydroxy-5,10-dodecadiyn-1-yl)-3,5,6-trimethyl-
Lopac0_000026
BSPBio_001266
KBioGR_000606
KBioSS_000606
SCHEMBL522781
KBio2_000606
KBio2_003174
KBio2_005742
KBio3_001071
KBio3_001072
Bio2_000473
Bio2_000953
GLXC-01554
HMS1362P07
HMS1792P07
HMS1990P07
HMS2089P21
HMS2232L19
HMS3260E13
HMS3403P07
Tox21_110072
Tox21_500026
BDBM50103621
EI-216
LMFA05000652
AKOS016009886
Tox21_110072_1
CCG-204122
LP00026
SDCCGSBI-0050015.P002
IDI1_002228
NCGC00015053-01
NCGC00015053-02
NCGC00015053-03
NCGC00015053-04
NCGC00015053-06
NCGC00015053-07
NCGC00015053-08
NCGC00015053-09
NCGC00015053-10
NCGC00024221-03
NCGC00024221-04
NCGC00024221-05
NCGC00024221-06
NCGC00260711-01
HY-12886
MS-24879
DB-056462
CS-0012749
EU-0100026
NS00126251
A 3711
C01349
D03882
G12480
AB00382986-12
SR-01000000084
SR-01000000084-2
BRD-K08290224-001-14-5
Q27105638
635-956-3