Determine the necessary mass, volume, or concentration for preparing a solution.
for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Desiccated Ships Wet ice 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.
Prohexadione (BX-112) calcium is a plant growth regulator. Prohexadione inhibits gibberellin biosynthesis of plants
In Vitro
Prohexadione (1 mM) calcium inhibits JMJD2A demethylase activity. Prohexadione (1-2 mM) calcium induces the differentiation of mouse neurospheres into neurons. Prohexadione (100 mg/L, sprayed on the leaves) calcium alleviates saline-alkali stress in soybean seedlings. Prohexadione calcium induces structural resistance to fire blight infection in potted apple trees . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Form:Solid
IC50& Target:Gibberellin biosynthesis
| Canonical Smiles | CCC(=C1C(=O)CC(CC1=O)C(=O)[O-])[O-].[Ca+2] |
|---|---|
| IUPAC Name | calcium;4-(1-oxidopropylidene)-3,5-dioxocyclohexane-1-carboxylate |
| InChIKey | NLKUPINTOLSSLD-UHFFFAOYSA-L |
| INCHI | 1S/C10H12O5.Ca/c1-2-6(11)9-7(12)3-5(10(14)15)4-8(9)13;/h5,11H,2-4H2,1H3,(H,14,15);/q;+2/p-2 |
| Isomeric SMILES | CCC(=C1C(=O)CC(CC1=O)C(=O)[O-])[O-].[Ca+2] |
| PubChem CID | 12001831 |
| Molecular Weight | 250.26 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Vinylogous acids |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Vinylogous acids |
| Alternative Parents | Cyclic ketones Carboxylic acid salts Organic calcium salts Monocarboxylic acids and derivatives Enolates Carboxylic acids Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Vinylogous acid - Carboxylic acid salt - Cyclic ketone - Ketone - Carboxylic acid derivative - Organic calcium salt - Carboxylic acid - Enolate - Monocarboxylic acid or derivatives - Carbonyl group - Organooxygen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as vinylogous acids. These are organic compounds containing a hydroxyl group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety. |
| External Descriptors | Not available |
| Molecular Weight | 250.260 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | 250.015 Da |
| Monoisotopic Mass | 250.015 Da |
| Topological Polar Surface Area | 97.300 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 327.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |