Interesting facts
Interesting Facts about 2,3-Dihydroxybutanedioic Acid
2,3-Dihydroxybutanedioic acid, commonly known as tartaric acid, is a fascinating organic compound with a rich history and various applications. Here are some intriguing aspects to consider:
- Natural Occurrence: Tartaric acid is naturally found in many plants, particularly in grapes, which makes it an essential ingredient in winemaking. Its presence contributes to the acidity, flavor, and stability of wine.
- Optical Activity: The compound exhibits optical activity due to its asymmetrical hydrogen and hydroxyl groups. This property leads to the existence of two enantiomers, which can have different effects in biological systems and can be observed through polarimetry.
- Biochemical Significance: Tartaric acid serves as a critical intermediate in various metabolic pathways. For instance, it can participate in carbohydrate metabolism and is involved in the citric acid cycle, a vital process for energy production in living organisms.
- Culinary Uses: Besides its role in winemaking, tartaric acid is also used as a food additive. It acts as a stabilizing agent in cream of tartar, helping to maintain the structure of whipped egg whites and preventing sugar from crystallizing.
- Industrial Applications: The compound is utilized in the manufacture of cosmetics, pharmaceuticals, and certain cleaning agents. Its ability to act as a buffering agent helps maintain pH levels in various formulations.
- Historical Context: Historically, the use of tartaric acid dates back to ancient Egyptians, who incorporated it into their food processing techniques. Its role in creating stable wine has been recognized for centuries.
In summary, 2,3-dihydroxybutanedioic acid is more than just a simple organic compound; it embodies a blend of natural occurrence, biochemical importance, and industrial utility. This versatility makes it a subject of continued interest in both scientific research and practical applications.
Synonyms
DL-Tartaric acid
2,3-Dihydroxysuccinic acid
tartaric acid
2,3-Dihydroxybutanedioic acid
526-83-0
133-37-9
Racemic acid
Uvic acid
Traubensaure
Racemic tartaric acid
DL-Tartrate
Paratartaric acid
Paratartaric aicd
BUTANEDIOIC ACID, 2,3-DIHYDROXY-
Resolvable tartaric acid
NSC62778
Tartaric acid D,L
CHEBI:15674
dl-2,3-dihydroxybutanedioic acid
(2RS,3RS)-Tartaric acid
tartrate
E-7050 (2S,3S)-2,3-dihydroxysuccinic acid
NSC 148314
Tartaric acid, L-(+)-
C4H6O6
1007601-97-9
Butanedioic acid, 2,3-dihydroxy-(R*,R*)-(.+/-.)-
Butanedioic acid, 2,3-dihydroxy-, (R*,R*)-
868-14-4
MFCD00071626
Tartaric acid (VAN)
Kyselina vinna [Czech]
NSC155080
Tartaric acid [USAN:JAN]
2,3-Dihydrosuccinic acid
(.+-.)-Tartaric acid
DTXSID5046986
d-alpha,beta-Dihydroxysuccinic acid
Butanedioic acid, 2,3-dihydroxy-; 2,3-Dihydroxybutanedioic acid
NSC-148314
Kyselina 2,3-dihydroxybutandiova [Czech]
(+) tartaric acid
(-) tartaric acid
MFCD00064206
1,2-dicarboxylic acid
WLN: QVYQYQVQ
(-) D-Tartaric acid
Sal tartar (Salt/Mix)
Tartaric acid, (DL)-
Butanedioic acid, 2,3-dihydroxy- (R-(R*,R*))-
Malic acid, 3-hydroxy-
2,3-Dihydroxysuccinicacid
Succinic acid,3-dihydroxy
SCHEMBL848
bmse000167
Succinic acid,3-dihydroxy-
(.+/-.)-Tartaric acid
Oprea1_827092
TARTARIC ACID, (L)
Tartaric acid, (.+-.)-
Butanedioic acid,3-dihydroxy-
CHEMBL333714
Dihydroxysuccinic acid, (DL)-
Tartaric acid, (.+/-.)-
DTXCID3026986
DTXSID501031477
HMS3370M15
(+)-2,3-dihydroxybutanedioic acid
BCP14303
HY-N2436
Tox21_302052
BBL011588
NSC133735
NSC148314
NSC608773
s2997
STK387106
2,3-Dihydroxysuccinic acid, (DL)-
3-carboxy-2,3-dihydroxypropanoic acid
AKOS000120086
AKOS016844048
FT34258
NSC-133735
NSC-608773
SB44180
SB44181
SMP2_000051
D(-)-Tartaric acid; DL-Tartaric acid;
d-.alpha.,.beta.-Dihydroxysuccinic acid
NCGC00256063-01
NCGC00347131-03
AS-10983
CAS-133-37-9
DA-62945
NCI60_001102
(+)-2,3-dihydroxy-1,4-butanedioic acid
DB-016129
DB-016159
DB-042899
CS-0022654
NS00078822
NS00079339
NS00079739
T0001
(+/-)-2,3-dihydroxy-1,4-butanedioic acid
2,3-dihydroxy-[R-(R*,R*)]-Butanedioicacid
EN300-19175
Butanedioic acid,3-dihydroxy- [R-(R*,R*)]-
Q194322
Butanedioic acid,3-dihydroxy-, (R*,R*)-(.+-.)-
F2191-0230
Z104473036
(2S,3S)-(-)-Tartaric acid; D(-)-Threaric acid;D(-)-Dihydroxysuccinic acid
Copper, mixt. with [R-(R*,R*)]-2,3-dihydroxybutanedioic acid monopotassium salt
Solubility of 2,3-Dihydroxybutanedioic Acid
2,3-Dihydroxybutanedioic acid, with the chemical formula C4H6O6, exhibits interesting solubility characteristics due to its structural features. As a dicarboxylic acid with hydroxyl groups, it has the ability to interact significantly with polar solvents.
Key Points about Solubility:
To sum up, the solubility of 2,3-dihydroxybutanedioic acid in water supports its functionality in biochemical processes and applications in various fields, showcasing the importance of molecular structure in determining solubility behavior.