≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
studies utilized an effective in vitro assay for retinyl palmitate hydrolase (RPH) activity plasma renin activity determined The NADH-cytochrome b5 reductase activity decreased strikingly as the buffer or salt concentration in the assay mixture was increased, and the optimal pH for the reduction of cytochrome b5 with NADH was determined to be 6.6 in Tris-maleate buffer of constant ionic strength. A series of tris-maleate-buffered salt solutions, from pH 6.4 to 8.9 was used to assess the effect of pH on the two hour leakage of creatine kinase (CK) from isolated mouse heart.
| Canonical Smiles | C(C(CO)(CO)N)O.C(=CC(=O)O)C(=O)O |
|---|---|
| IUPAC Name | 2-amino-2-(hydroxymethyl)propane-1,3-diol;(Z)-but-2-enedioic acid |
| InChIKey | HTMWOUBCEZXSHN-BTJKTKAUSA-N |
| INCHI | 1S/C4H11NO3.C4H4O4/c5-4(1-6,2-7)3-8;5-3(6)1-2-4(7)8/h6-8H,1-3,5H2;1-2H,(H,5,6)(H,7,8)/b;2-1- |
| Isomeric SMILES | C(C(CO)(CO)N)O.C(=C\C(=O)O)\C(=O)O |
| PubChem CID | 16218780 |
| Molecular Weight | 237.21 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Dicarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dicarboxylic acids and derivatives |
| Alternative Parents | Unsaturated fatty acids 1,2-aminoalcohols Carboxylic acids Primary alcohols Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Not available |
| Substituents | Fatty acyl - Fatty acid - Unsaturated fatty acid - Dicarboxylic acid or derivatives - 1,2-aminoalcohol - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. |
| External Descriptors | Not available |
| Solubility | Soluble in Water: 0.5 M at 20° C |
|---|---|
| Melt Point(°C) | 104-106° C |
| Molecular Weight | 237.210 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 5 |
| Exact Mass | 237.085 Da |
| Monoisotopic Mass | 237.085 Da |
| Topological Polar Surface Area | 161.000 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 173.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 2 |
I22081032