Interesting facts
Interesting Facts about 2-Sulfanylbutanedioic Acid
2-Sulfanylbutanedioic acid, also known as *thiobutyric acid*, is a fascinating compound with intriguing properties and potential applications. Here are some interesting highlights:
- Chemical Structure: This compound comprises a butanedioic acid backbone with a sulfanyl (thiol) group, making it unique in its reactivity and behavior.
- Biological Relevance: The presence of the thiol group enables this compound to participate in various biochemical processes, including the synthesis of cysteine and other vital amino acids in living organisms.
- Potential Applications: Researchers are exploring its utility in drug development, particularly as a building block for compounds that can target specific biological pathways.
- Environmental Importance: Compounds like 2-sulfanylbutanedioic acid may also play a role in various biochemical cycles, thus contributing to our understanding of ecological interactions.
- Odor Profile: The characteristic sulfanyl group is known for its strong odor, reminiscent of rotten eggs. This feature can be a significant consideration in chemical handling and storage.
In summary, 2-sulfanylbutanedioic acid is not just a simple organic compound. Its structural characteristics, biological significance, and potential applications make it a noteworthy subject for further research in the fields of organic chemistry and biochemistry. As scientists continue to delve into the properties of such compounds, the possibilities for innovation and discovery remain boundless.
Synonyms
Mercaptosuccinic acid
70-49-5
Thiomalic acid
2-sulfanylbutanedioic acid
2-Mercaptosuccinic acid
2-Thiomalic acid
DL-Mercaptosuccinic acid
Butanedioic acid, mercapto-
Monomercaptosuccinic acid
Malic acid, 2-thio-
Mercaptosuccinate
USAF EK-P-6297
SUCCINIC ACID, MERCAPTO-
USAF M-2
2-Sulfanylsuccinic acid
NSC 7302
butanedioic acid, 2-mercapto-
(1)-Mercaptosuccinic acid
EINECS 200-736-4
EINECS 211-423-7
BRN 1099858
AI3-22956
DL-THIOMALIC ACID
NSC-7302
MFCD00004860
alpha-Mercaptosuccinic acid
94239W5L4H
THIOMALIC ACID [MI]
.alpha.-Mercaptosuccinic acid
(+/-)-Mercaptosuccinic acid
CHEBI:38705
4-03-00-01130 (Beilstein Handbook Reference)
SODIUM AUROTHIOMALATE IMPURITY C [EP IMPURITY]
NSC41809
mercaptobutanedioic acid
SODIUM AUROTHIOMALATE IMPURITY C (EP IMPURITY)
UNII-94239W5L4H
Malic acid, 2thio
HSTM
2Mercaptosuccinic acid
Succinic acid, mercapto
WLN: SHYVQ1VQ
(1)Mercaptosuccinic acid
2-Mercapto-succinic acid
Butanedioic acid, mercapto
2-Sulfanylsuccinic acid #
Butanedioic acid, 2mercapto
Mercaptosuccinic acid, 97%
MLS006011445
SCHEMBL133541
CHEMBL4303414
DTXSID20861615
NSC7302
2-Sulphanylbutane-1,4-dioic acid
STR07420
BBL011516
STL146632
AKOS000120969
AKOS016042329
CS-W010986
SB45438
1-Sulfanylethane-1,2-dicarboxylic acid
NCI60_003949
PD062592
SMR001826671
M0064
NS00020699
EN300-20552
D70319
SBI-0653860.0001
SR-01000945206
Q7784684
SR-01000945206-1
BRD-A43435802-001-01-2
BRD-A43435802-001-02-0
Mercaptosuccinic acid, Vetec(TM) reagent grade, 97%
F2191-0218
Z104478826
Mercaptosuccinic acid, ReagentPlus(R), >=99.0% (HPLC)
200-736-4
Solubility of 2-sulfanylbutanedioic acid (C4H6O4S)
2-sulfanylbutanedioic acid, also known as thiodiacetic acid, exhibits unique solubility properties due to its chemical structure. Understanding its solubility can shed light on its potential applications and interactions in various environments.
Solubility Characteristics
The solubility behavior of this compound can be summarized by the following quote: "Compounds with polar functional groups have enhanced interaction with water, leading to better solubility." This principle is essential when considering the various chemical processes where 2-sulfanylbutanedioic acid may be utilized.
Overall, understanding the solubility of 2-sulfanylbutanedioic acid not only aids in its effective use in synthesis and applications but also emphasizes its role in biochemical systems where solubility is a critical factor.