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Thiamine

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Identification
Molecular formula
C8H11NO3S
CAS number
59-43-8
IUPAC name
3-(2-carboxyethylsulfanyl)propanoic acid
State
State

At room temperature, Thiamine exists as a solid. It should be stored in a cool, dry place to ensure its stability and longevity. Thiamine is known for its ease of solubility in water but not in other solvents like ether or chloroform due to its polar nature.

Melting point (Celsius)
248.00
Melting point (Kelvin)
521.15
Boiling point (Celsius)
318.60
Boiling point (Kelvin)
591.75
General information
Molecular weight
180.22g/mol
Molar mass
180.2150g/mol
Density
1.3800g/cm3
Appearence

White crystalline solid, sometimes appearing as a powder. It is generally a stable compound under normal conditions when it is free of moisture and exposed to air only. However, it can decompose if exposed to heat or high pH levels.

Comment on solubility

Solubility of 3-(2-carboxyethylsulfanyl)propanoic Acid

The solubility of 3-(2-carboxyethylsulfanyl)propanoic acid can be analyzed based on its chemical structure and functional groups. This compound includes both acidic and polar characteristics, which typically enhance solubility in polar solvents, particularly water. Here are some key points to consider:

  • Polar Functional Groups: The presence of carboxylic acid groups (-COOH) is known to increase solubility in water due to hydrogen bonding.
  • Hydrophilic Nature: The attached -CH2 and -SH groups also contribute to the overall hydrophilicity of the compound, promoting its dissolution in aqueous solutions.
  • pH Dependence: The ionization of the carboxylic acid group under varying pH levels affects solubility. Increased pH can lead to greater ionization, thus enhancing solubility in water.
  • Concentration Effects: As the concentration of 3-(2-carboxyethylsulfanyl)propanoic acid increases, solubility may reach a saturation point, which is an important factor in various applications.

In conclusion, 3-(2-carboxyethylsulfanyl)propanoic acid is expected to exhibit moderate to high solubility in water, especially due to its acidic functional groups and overall polar nature. Understanding its solubility behavior is crucial for its practical use in biochemical applications.

Interesting facts

Interesting Facts about 3-(2-Carboxyethylsulfanyl)propanoic Acid

3-(2-Carboxyethylsulfanyl)propanoic acid is a fascinating organic compound that provides a myriad of interesting insights into the world of biochemistry and organic chemistry.

Biological Significance

This compound is particularly notable due to its role as a potential metabolic precursor. It has been implicated in various biochemical processes, especially in the synthesis of important biomolecules.

Structure and Functional Groups

The unique structure of 3-(2-carboxyethylsulfanyl)propanoic acid includes:

  • Carboxylic Acid Group: Which contributes to its acidic properties and reactivity.
  • Thioether Moiety: This functional group is essential for certain biochemical pathways and can enhance biological activity.

Research Applications

There is ongoing research exploring the potential of this compound in:

  • Drug Development: Investigating its efficacy in pharmaceuticals targeting specific metabolic pathways.
  • Metabolic Studies: Understanding its role in cellular metabolism and how it influences certain disease states.

Quote from a Researcher

A notable researcher stated: "The role of 3-(2-carboxyethylsulfanyl)propanoic acid in metabolic processes is an exhilarating area of study, revealing insights into the biochemical machinery of life."

Conclusion

As we delve deeper into the properties and functions of 3-(2-carboxyethylsulfanyl)propanoic acid, we uncover vital details that not only enrich our understanding of organic compounds but also open doors to novel therapeutic strategies. The interplay between structure and functionality makes this compound a cornerstone for upcoming research in biochemical innovation.

Synonyms
3,3'-Thiodipropionic acid
111-17-1
THIODIPROPIONIC ACID
Propanoic acid, 3,3'-thiobis-
Tyox A
Bis(2-carboxyethyl) sulfide
TDPA
Thiodihydracrylic acid
3,3'-Thiodipropanoic acid
4-Thiaheptanedioic acid
3,3'-Thiodi(propionic acid)
Sulfide, bis(2-carboxyethyl)
3,3'-Thiobis(propanoic acid)
Thiahydracrylic acid
3,3-thiodipropionic acid
Propionic acid, 3,3'-thiodi-
3-[(2-carboxyethyl)sulfanyl]propanoic acid
Diethyl sulfide 2,2'-dicarboxylic acid
NSC 8166
Kyselina 3,3-thiodipropionova
CCRIS 3288
HSDB 858
3-(2-carboxyethylsulfanyl)propanoic acid
EINECS 203-841-3
3,3'-Thiobispropanoic acid
Thiobispropanoic acid
Kyselina 3,3-thiodipropionova [Czech]
3BBK323ED8
DTXSID8044200
AI3-25276
Kyselina beta,beta'-thiodipropionova [Czech]
NSC-8166
Kyselina beta,beta'-thiodipropionova
3,3'-Thiobis-propanoic acid
MLS000105101
INS NO.388
DTXCID6024200
INS-388
EC 203-841-3
THIODIPROPIONIC ACID [HSDB]
.beta.,.beta.'-Thiodipropionic acid
NSC-65523
3,3'-THIODIPROPIONIC ACID [MI]
Kyselina .beta.,.beta.'-thiodipropionova
SMR000055030
E-388
KYSELINA BETA,BETA'-THIODIPROPIONOVA (CZECH)
MFCD00002781
UNII-3BBK323ED8
4Thiaheptanedioic acid
4-Thiaheptanedioio acid
3,3-Thiodipropionicacid
Opera_ID_1107
3,3'thiodipropionic acid
Bis(2carboxyethyl) sulfide
WLN: QV2S2VQ
Propionic acid,3'-thiodi-
NCIOpen2_002942
Propanoic acid,3'-thiobis-
Sulfide, bis(2carboxyethyl)
Kyselina 3,3thiodipropionova
SCHEMBL28696
3,3\'-Thiodipropionic acid
Propionic acid, 3,3'thiodi
3,3'-Thiodi-Propionic acid
3,3'Thiobis(propanoic acid)
Propanoic acid, 3,3'thiobis
beta,beta'-Thiodipropionic acid
CHEMBL1569439
NSC8166
CHEBI:165380
3,3'-Thiodipropionic acid, 8CI
beta ,beta '-Thiodipropionic acid
HMS2358F24
Kyselina beta,beta'thiodipropionova
3,3'-Thiodipropionic acid, 97%
3,3'-thiodipropionic acid, 99%
THIODIPROPIONIC ACID [INCI]
BCP34296
Tox21_300987
AKOS000120885
Diethyl sulfide 2,2'dicarboxylic acid
AT21042
CS-W017330
Diethyl sulfide b,b'-dicarboxylic acid
3-(2-carboxyethylsulanyl)propanoic acid
NCGC00092735-02
NCGC00254889-01
BS-14446
CAS-111-17-1
E388
DB-060072
NS00007804
T0204
EN300-19982
Q2823309
F0264-0039
Z104476280
Bis(2-carboxyethyl) sulfide;Propanoic acid, 3,3'-thiobis-;Thiodipropionic acid