Interesting facts
Interesting Facts about 1,4-Benzoquinone
1,4-Benzoquinone, also known as p-benzoquinone, is an intriguing compound with several notable characteristics and applications. Here are some key points that highlight its significance in chemistry:
- Oxidation-Reduction Reactions: This compound plays a crucial role in various oxidation-reduction reactions, often acting as an oxidizing agent. Its ability to accept electrons makes it a valuable reagent in organic synthesis.
- Natural Occurrence: 1,4-Benzoquinone is not just a synthetic compound; it can also be found in nature, particularly in certain plants and as a product of the degradation of organic matter. Its presence in natural substances highlights its ecological importance.
- Biochemical Significance: In the field of biochemistry, 1,4-Benzoquinone is involved in important metabolic pathways. For instance, it is a key intermediate in the biosynthesis of certain hormones in plants, showcasing its role in biological processes.
- Color and Aromatic Nature: The compound is remarkable for its vibrant color and its contribution to the aromatic character of various substances. This property has made it an interesting subject of study in the development of dyes and pigments.
- Polymerization Potential: Due to its reactive characteristics, 1,4-Benzoquinone can polymerize under certain conditions, leading to the formation of various polymeric materials. This feature opens up potential applications in the field of materials science.
- Safety Considerations: While 1,4-Benzoquinone has various benefits, it is important to handle this compound with caution. It can be a skin and respiratory irritant, emphasizing the need for appropriate safety measures in laboratory settings.
In summary, 1,4-Benzoquinone is a multifaceted compound that crosses the boundaries of organic chemistry, biochemistry, and materials science. Its diverse applications and natural occurrence make it a fascinating topic of study for chemists and biology enthusiasts alike.
Synonyms
p-benzoquinone
1,4-BENZOQUINONE
Benzoquinone
Quinone
106-51-4
p-Quinone
cyclohexa-2,5-diene-1,4-dione
para-Benzoquinone
Chinone
2,5-Cyclohexadiene-1,4-dione
Cyclohexadienedione
para-Quinone
1,4-Benzoquine
1,4-Cyclohexadienedione
1,4-Dioxybenzene
Steara pbq
p-Chinon
Benzo-chinon
Benzo-1,4-quinone
1,4-Diossibenzene
Chinon
1,4-Dioxy-benzol
1,4-Cyclohexadiene dioxide
semiquinone radicals
Caswell No. 719C
Semiquinone anion
RCRA waste number U197
NCI-C55845
CCRIS 933
USAF P-220
HSDB 1111
Cyclohexadiene-1,4-dione
1,4-Benzochinon
EINECS 203-405-2
MFCD00001591
NSC 36324
NSC-36324
UN2587
EPA Pesticide Chemical Code 059805
UNII-3T006GV98U
[1,4]benzoquinone
DTXSID6020145
CHEBI:16509
AI3-09068
Quinone1,4-Benzoquinone
QUINONE [MI]
QUINONE [WHO-DD]
PARA-QUINONE [IARC]
CHEMBL8320
DTXCID40145
2,5-cyclohexadiene-1-4-dione
3225-29-4
1,4-BENZOQUINONE [HSDB]
EC 203-405-2
3T006GV98U
1,4-BENZOQUINONE [USP-RS]
UN 2587
1,4-Benzoquinone, 99%
PARA-QUINONE (IARC)
2,5-Cyclohexadiene-1,4-dione, radical ion(1-)
p-Chinon [German]
Benzo-chinon [German]
1,4-Benzoquinone; SKF-21232
1,4-BENZOQUINONE (USP-RS)
Chinon [Dutch, German]
1,4 benzoquinone
CAS-106-51-4
1,4-Dioxy-benzol [German]
1,4-Diossibenzene [Italian]
RCRA waste no. U197
parabenzochinon
paraQuinone
pBenzoquinone
pChinon
pQuinone
parabenzoquinone
p-benzo-quinone
C6H4O2
1,4benzoquinone
1,4Dioxybenzene
1,4Dioxybenzol
1,4Benzoquine
1,4Diossibenzene
Quinone; p-BQ
NSC36324
Caswell No 719C
2,4-dione
p-BQ
1,4Cyclohexadienedione
p-Benzoquinone (OSHA)
Benzo-1,4-quinone #
Lopac-B-1266
1,4Cyclohexadiene dioxide
Quinone (ACGIH:OSHA)
Benzoquinone [UN2587]
Epitope ID:116219
WLN: L6V DVJ
Chinon(DUTCH, GERMAN)
2,5Cyclohexadiene1,4dione
cid_4650
Lopac0_000120
SCHEMBL18103
MLS002454445
GTPL6307
BDBM22774
CHEBI:39439
HMS2230N13
HMS3260G22
Quinone; 1,4-Cyclohexanedienedione
Tox21_202020
Tox21_302970
Tox21_500120
BBL010327
Benzoquinone [UN2587] [Poison]
c0261
STK398389
AKOS000119965
AKOS025243267
CCG-204215
FB01020
LP00120
SDCCGSBI-0050108.P002
2,5-CYCLOHEXANDIEN-1,4-DIONE
p-Benzoquinone, reagent grade, >=98%
NCGC00015139-01
NCGC00015139-02
NCGC00015139-03
NCGC00015139-04
NCGC00015139-05
NCGC00015139-06
NCGC00015139-07
NCGC00015139-10
NCGC00091053-01
NCGC00091053-02
NCGC00091053-03
NCGC00256505-01
NCGC00259569-01
NCGC00260805-01
SMR000326659
VS-02448
DS-000613
B0089
B0887
EU-0100120
NS00003185
EN300-19699
B 1266
C00472
A801452
Q402719
SR-01000075705
SR-01000075705-1
Z104474802
1,4-Benzoquinone, pharmaceutical secondary standard; traceable to USP
1,4-Benzoquinone, United States Pharmacopeia (USP) Reference Standard
cyclohexa-2,5-diene-1,4-dione; QUINONE RING OF THE PLASTOQUINONE 9
1,4-Benzoquinone, Pharmaceutical Secondary Standard; Certified Reference Material
1,4-Benzoquinone;2,5-Cyclohexadiene-1,4-dione; Quinone; 2,5-Cyclohexadiene-1,4-dione
946-235-0
Solubility of 1,4-Benzoquinone (C6H4O2)
1,4-Benzoquinone is a fascinating compound when it comes to solubility characteristics. This molecule exhibits interesting behavior in various solvents due to its unique chemical structure. Here are some key points regarding its solubility:
In summary, the solubility of 1,4-benzoquinone varies significantly with solvent choice, showcasing its polar and nonpolar interactions. This compound's ability to dissolve in polar solvents while struggling in nonpolar ones offers intriguing insights into its chemical behavior.