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Basic Description
| Synonyms | sulfobutanedioic acid | Sulphosuccinic acid | 2-Sulfobutanedioic acid | 2-Sulfosuccinic acid |
|---|---|
| Specifications & Purity | 70 wt. % in H2O |
| Storage Temp | Room temperature |
| Shipped In | Normal |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Lipids and lipid-like molecules
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Class
Fatty Acyls
- Subclass Fatty acids and conjugates
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Class
Fatty Acyls
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Superclass
Lipids and lipid-like molecules
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acids and conjugates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thia fatty acids |
| Alternative Parents | Dicarboxylic acids and derivatives Sulfonyls Organosulfonic acids Alkanesulfonic acids Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Thia fatty acid - Dicarboxylic acid or derivatives - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Alkanesulfonic acid - Carboxylic acid derivative - Carboxylic acid - Carbonyl group - Organosulfur compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as thia fatty acids. These are fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain. |
| External Descriptors | Not available |
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Names and Identifiers
| Pubchem Sid | 504753027 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504753027 |
| IUPAC Name | 2-sulfobutanedioic acid |
| INCHI | InChI=1S/C4H6O7S/c5-3(6)1-2(4(7)8)12(9,10)11/h2H,1H2,(H,5,6)(H,7,8)(H,9,10,11) |
| InChIKey | ULUAUXLGCMPNKK-UHFFFAOYSA-N |
| Smiles | C(C(C(=O)O)S(=O)(=O)O)C(=O)O |
| Isomeric SMILES | C(C(C(=O)O)S(=O)(=O)O)C(=O)O |
| PubChem CID | 21220 |
| UN Number | 3265 |
| Molecular Weight | 198.15 |
| Beilstein | 1727687 |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 C2505459 |
Certificate of Analysis | Jun 29, 2024 | S462861 |
| B24231137 |
Certificate of Analysis | Jan 26, 2024 | S462861 |
| B24231138 |
Certificate of Analysis | Jan 26, 2024 | S462861 |
| G2327304 |
Certificate of Analysis | Jul 20, 2023 | S462861 |
| E2305445 |
Certificate of Analysis | Apr 21, 2023 | S462861 |
Chemical and Physical Properties
| Refractive Index | n20/D 1.449 |
|---|---|
| Flash Point(°F) | Not applicable |
| Flash Point(°C) | Not applicable |
| Molecular Weight | 198.150 g/mol |
| XLogP3 | -1.800 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | 197.983 Da |
| Monoisotopic Mass | 197.983 Da |
| Topological Polar Surface Area | 137.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 283.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Citations of This Product
| 1. Henan Huang, Fengying Li, Chenglong Yu, Hansun Fang, Xinchun Guo, Danping Li. (2021) Anion-/cationic compounds enhance the dispersion of flow electrodes to obtain high capacitive deionization performance. DESALINATION, 515 (115182). |
| 2. Danping Li, Xun-an Ning, Yiqian Yuan, Yanxiang Hong, Jianpei Zhang. (2020) Ion-exchange polymers modified bacterial cellulose electrodes for the selective removal of nitrite ions from tail water of dyeing wastewater. Journal of Environmental Sciences, 91 (62). |
| 3. Muhammad Irfan, Yaoming Wang, Tongwen Xu. (2020) Novel electrodialysis membranes with hydrophobic alkyl spacers and zwitterion structure enable high monovalent/divalent cation selectivity. CHEMICAL ENGINEERING JOURNAL, 383 (123171). |
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