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Moligand™, 20% w/v in aqueous solution Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Chlorhexidine digluconate solution is a bis(biguanide) family cationic broad spectrum antibiotic. Studies indicate that Chlorhexidine digluconate solution functions, via destabilization of the outer bacterial membrane, which resulted in the release of periplasmic enzymes in gram negative bacteria. In addition, Chlorhexidine digluconate solution inhibits oxygen utilization which leads to a reduction in bacterial ATP. These studies also indicate that the inner membrane in gram negative bacteria was not affected by the solution, however there was inhibition of active transport for small molecules entering the cell. Furthermore, Chlorhexidine digluconate solution is very effective against bacteria such as|Propionibacterium, Selenomonas|, and cocci resembling|Veillonella|.
| Pubchem Sid | 504764816 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504764816 |
| Canonical Smiles | C1=CC(=CC=C1NC(=NC(=NCCCCCCN=C(N)N=C(N)NC2=CC=C(C=C2)Cl)N)N)Cl.C(C(C(C(C(C(=O)O)O)O)O)O)O.C(C(C(C(C(C(=O)O)O)O)O)O)O |
| IUPAC Name | (1E)-2-[6-[[amino-[(E)-[amino-(4-chloroanilino)methylidene]amino]methylidene]amino]hexyl]-1-[amino-(4-chloroanilino)methylidene]guanidine;(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acid |
| InChIKey | YZIYKJHYYHPJIB-UUPCJSQJSA-N |
| INCHI | 1S/C22H30Cl2N10.2C6H12O7/c23-15-5-9-17(10-6-15)31-21(27)33-19(25)29-13-3-1-2-4-14-30-20(26)34-22(28)32-18-11-7-16(24)8-12-18;2*7-1-2(8)3(9)4(10)5(11)6(12)13/h5-12H,1-4,13-14H2,(H5,25,27,29,31,33)(H5,26,28,30,32,34);2*2-5,7-11H,1H2,(H,12,13)/t;2*2-,3-,4+,5-/m.11/s1 |
| Isomeric SMILES | C1=CC(=CC=C1N/C(=N/C(=NCCCCCCN=C(/N=C(/NC2=CC=C(C=C2)Cl)\N)N)N)/N)Cl.C(O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(=O)O.C(O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(=O)O |
| PubChem CID | 9552081 |
| Molecular Weight | 897.76 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Sugar acids and derivatives |
| Alternative Parents | Medium-chain hydroxy acids and derivatives Medium-chain fatty acids Beta hydroxy acids and derivatives Biguanides Chlorobenzenes Hydroxy fatty acids Alpha hydroxy acids and derivatives Aryl chlorides Monosaccharides Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Polyols Carboximidamides Carboxylic acids Monocarboxylic acids and derivatives Organopnictogen compounds Primary alcohols Organochlorides Hydrocarbon derivatives Organic oxides Imines Carbonyl compounds |
| Molecular Framework | Not available |
| Substituents | Gluconic_acid - Medium-chain hydroxy acid - Medium-chain fatty acid - Hydroxy fatty acid - Halobenzene - Chlorobenzene - Biguanide - Beta-hydroxy acid - Benzenoid - Monosaccharide - Aryl halide - Aryl chloride - Hydroxy acid - Alpha-hydroxy acid - Fatty acid - Fatty acyl - Monocyclic benzene moiety - Secondary alcohol - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Carboxylic acid - Carboximidamide - Polyol - Monocarboxylic acid or derivatives - Organic oxide - Organopnictogen compound - Carbonyl group - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organonitrogen compound - Organochloride - Imine - Organohalogen compound - Alcohol - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group. |
| External Descriptors | D-gluconate adduct - organochlorine compound |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Apr 03, 2026 | C346980 | |
| Certificate of Analysis | Aug 28, 2025 | C346980 | |
| Certificate of Analysis | Aug 28, 2025 | C346980 | |
| Certificate of Analysis | Aug 28, 2025 | C346980 | |
| Certificate of Analysis | Aug 28, 2025 | C346980 | |
| Certificate of Analysis | Aug 28, 2025 | C346980 | |
| Certificate of Analysis | May 31, 2024 | C346980 | |
| Certificate of Analysis | May 31, 2024 | C346980 | |
| Certificate of Analysis | May 31, 2024 | C346980 | |
| Certificate of Analysis | May 31, 2024 | C346980 | |
| Certificate of Analysis | May 22, 2023 | C346980 | |
| Certificate of Analysis | May 22, 2023 | C346980 | |
| Certificate of Analysis | May 22, 2023 | C346980 | |
| Certificate of Analysis | May 22, 2023 | C346980 | |
| Certificate of Analysis | May 22, 2023 | C346980 | |
| Certificate of Analysis | May 22, 2023 | C346980 |
| Sensitivity | light & heat sensitive |
|---|---|
| Molecular Weight | 897.800 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 18 |
| Hydrogen Bond Acceptor Count | 16 |
| Rotatable Bond Count | 23 |
| Exact Mass | 896.32 Da |
| Monoisotopic Mass | 896.32 Da |
| Topological Polar Surface Area | 454.000 Ų |
| Heavy Atom Count | 60 |
| Formal Charge | 0 |
| Complexity | 819.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 2 |
| Covalently-Bonded Unit Count | 3 |
| 1. Meng Wei, QiQi Hu, Qi Xie, TianQi Wang, WeiLi Xie. (2026) Enhanced antimicrobial properties of POSS-modified composite resin with chlorhexidine-loaded bioactive glass. JOURNAL OF DENTISTRY, [PMID:] [10.1016/j.jdent.2026.106633] |
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