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Basic Description
| Synonyms | LeucoMalachiteGreen | Malachite green leuco base | Malachite green leuco | Leucomalachite green | 4,4'-Bis(dimethylamino)triphenylmethane | Leuco malachite green | Bis(p-dimethylaminophenyl)phenylmethane | Benzenamine,4,4'-(phenylmethylene)bis[N,N-dimethy |
|---|---|
| Specifications & Purity | ≥98% |
| Biochemical and Physiological Mechanisms | Leucomalachite green (LMG) is a chief metabolite of malachite green, a triphenylmethane dye that has been used generally as an antifungal drug in the fish industry. DNA adducts formed in livers of rats fed with leucomalachite green have been observed with |
| Storage Temp | Store at 2-8°C,Protected from light |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Leucomalachite Green is a triphenylmethane dye used to detect blood. A method for testing for the presence of leucomalachite green utilizing SDS-modified maghemite nanoparticles (γ-Fe(2)O(3)) has been described. Other studies have reported various protocols useful for determining the presence of Leucomalachite green in aquatic biological systems. Leucomalachite green has been used as a reagent in presumptive tests which are used to detect invisible blood stains. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
- Class Triphenyl compounds
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Superclass
Benzenoids
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Triphenyl compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triphenyl compounds |
| Alternative Parents | Dialkylarylamines Aniline and substituted anilines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Triphenyl compound - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Monocyclic benzene moiety - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety. |
| External Descriptors | Not available |
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Associated Targets(Human)
NR3C1
Tclin
Glucocorticoid receptor (14987 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
VDR
Tclin
Vitamin D receptor (26531 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
PPARG
Tclin
Peroxisome proliferator-activated receptor gamma (15191 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
THRB
Tclin
Thyroid hormone receptor beta-1 (7926 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
RXRA
Tclin
Retinoid X receptor alpha (3637 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
NR1H4
Tclin
Bile acid receptor FXR (6228 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Names and Identifiers
| Pubchem Sid | 488183910 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183910 |
| IUPAC Name | 4-[[4-(dimethylamino)phenyl]-phenylmethyl]-N,N-dimethylaniline |
| INCHI | InChI=1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3 |
| InChIKey | WZKXBGJNNCGHIC-UHFFFAOYSA-N |
| Smiles | CN(C)C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=C(C=C3)N(C)C |
| Isomeric SMILES | CN(C)C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=C(C=C3)N(C)C |
| WGK Germany | 3 |
| RTECS | CY1203055 |
| UN Number | 3077 |
| Molecular Weight | 330.47 |
| Beilstein | 2140506 |
| Reaxy-Rn | 2140506 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2140506&ln= |
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 |
|---|---|---|---|
 G2424381 |
Certificate of Analysis | Aug 08, 2024 | L102032 |
| E2318482 |
Certificate of Analysis | May 24, 2023 | L102032 |
| E2318520 |
Certificate of Analysis | May 24, 2023 | L102032 |
| E2318502 |
Certificate of Analysis | May 24, 2023 | L102032 |
| E2318498 |
Certificate of Analysis | May 24, 2023 | L102032 |
| E2318500 |
Certificate of Analysis | May 24, 2023 | L102032 |
| E2318477 |
Certificate of Analysis | May 24, 2023 | L102032 |
Chemical and Physical Properties
| Solubility | Soluble in water (<0.1 mg/ml), chloroform, ethanol (4 mg/ml), and toluene. |
|---|---|
| Sensitivity | Light & Air Sensitive |
| Melt Point(°C) | 100-102°C |
| Molecular Weight | 330.500 g/mol |
| XLogP3 | 5.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Exact Mass | 330.21 Da |
| Monoisotopic Mass | 330.21 Da |
| Topological Polar Surface Area | 6.500 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 342.000 |
| 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 | 1 |
Alternative Products
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Leucomalachite GreenStarting at $69.90
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Leucomalachite Green
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