- Carminic Acid
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2026-07-03
- CAS:1260-17-9
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 1000kg
- Carminic acid
-
- $72.00
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2026-05-11
- CAS:1260-17-9
- Purity: 90.52%
- Supply Ability: 10g
- Carminic Acid
-
- $10.00
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2026-03-20
- CAS:1260-17-9
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
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| | Carminic Acid Basic information |
| Product Name: | Carminic Acid | | Synonyms: | Carminic Acid ;3,5,6,8-Tetrahydroxy-1-methyl-9,10-dioxo-7-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-9,10-dihydroanthracene-2-carboxylic acid;Carminic acid (C.I. 75470) GR for analysis and for microscopy;ALUMINUM LAKE OF CARMINIC ACID;2-anthracenecarboxylicacid,7-beta-d-glucopyranosyl-9,10-dihydro-3,5,6,8-tetra;7-.beta.-D-glucopyranosyl-9,10-dihydro-3,5,6,8-tetrahydroxy-1-methyl-9,10-dioxo-2-Anthracenecarboxylicacid;7-alpha-d-glucopyranosyl-9,10-dihydro-3,5,6,8-tetrahydroxy-1-methyl-9,10-dioxo;carminicacid50% | | CAS: | 1260-17-9 | | MF: | C22H20O13 | | MW: | 492.39 | | EINECS: | 215-023-3 | | Product Categories: | Anthraquinones;Biochemistry;Glucose;Glycosides;Hydroxyanthraquinones;Sugars;Di-Terpenoids;Carbohydrates & Derivatives;Intermediates & Fine Chemicals;Pharmaceuticals | | Mol File: | 1260-17-9.mol |  |
| | Carminic Acid Chemical Properties |
| Melting point | 136 °C | | alpha | 15654 +51.6° (water) | | Boiling point | 506.2°C (rough estimate) | | density | 1.4504 (rough estimate) | | bulk density | 490kg/m3 | | refractive index | 1.6000 (estimate) | | Fp | 12℃ | | storage temp. | room temp | | solubility | 30g/l | | Colour Index | 75470 | | form | Crystalline Powder | | pKa | 1.62±0.20(Predicted) | | color | Red to dark red | | PH | 1.6 (10g/l, H2O, 20℃) | | Odor | Odorless | | PH Range | 4.8 - 6.2 | | Optical Rotation | [α]20/D +3.1°, c = 1 in H2O | | Water Solubility | 1.298g/L(room temperature) | | λmax | 495 nm | | ε(extinction coefficient) | ≥13000 at 222-228 nm in ethanol at 0.03g/L
≥18000 at 275-281nm in ethanol at 0.03g/L | | Merck | 14,1843 | | BRN | 71651 | | Major Application | diagnostic assay manufacturing
hematology
histology | | InChIKey | DGQLVPJVXFOQEV-JNVSTXMASA-N | | SMILES | Cc1c(C(O)=O)c(O)cc2C(=O)c3c(O)c(O)c([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)c(O)c3C(=O)c12 | | LogP | 1.532 (est) | | CAS DataBase Reference | 1260-17-9 | | EPA Substance Registry System | C.I. Natural Red 4 (1260-17-9) |
| | Carminic Acid Usage And Synthesis |
| Chemical Properties | red to dark red crystalline powder | | Chemical Properties | Cochineal extract is a concentrated solution obtained after removing alcohol from an aqueous–alcoholic extract of
cochineal (Dactylopius coccus Costa, also called Coccus cati L.). This extract is used as a color additive, the primary colorant being
carminic acid. | | History | CI Natural Red 4(CI 75470), is a red dye occurring as a glycoside in the body of the cochineal insect Dactylopius coccus of the order Homoptera, family Coccidae. This insect is native to Central and South America. The Aztecs had extracted the dye from the insect centuries before the coming of the Spaniards. For breeding purposes, the insects were collected in the autumn and carefully protected during the winter months. Cochineal was harvested after three months, and then the bugs were killed by immersion in hot water, by placing in hot ovens, or by exposure to the hot sun. The latter method produced the highest quality dye. At present, Peru and the Canary Islands are the main source of the dye. Until the advent of synthetic dyes, the principal use for carminic acid was for dyeing tin-mordanted wool or silk. Its aluminum lake, carmine, finds use in the coloring of foods. | | Uses | Carminic acid (C.I. 75470) For staining nuclei in histological sections. Used to prepare staining solutions.
CAS 1260-17-9, pH 1.6 (10g/l, HO, 20°C). | | Uses | A red glucosidal hydroxyanthrapurin, it is produced naturally within some insects as a defense mechanism. | | Uses | antineoplastic, glucosyltransferase inhibitor | | Definition | ChEBI: A tetrahydroxyanthraquinone that is that is 1,3,4,6-tetrahydroxy-9,10-anthraquinone substituted by a methyl group at position 8, a carboxy group at position 7 and a 1,5-anhydro-D-glucitol moiety at position 2 via a C-gly
osidic linkage. It is a natural dye isolated from several insects such as Dactylopius coccus. | | General Description | Dark purplish-brown mass or bright red or dark red powder. Darkens at 248°F. Deep red color in water. Yellow to violet in acidic aqueous solutions. | | Air & Water Reactions | Soluble in water [Hawley]. | | Reactivity Profile | CARMINE neutralizes bases in exothermic reactions. Incompatible with strong oxidizing agents. | | Fire Hazard | Flash point data for CARMINE are not available. CARMINE is probably combustible. | | Purification Methods | Carminic acid forms red prisms from EtOH. It gives a red colour in Ac2O and yellow to violet in acidic solution. UV: max (H2O) 500nm ( 6,800); (0.02N HCl) 490-500nm ( 5,800) and (0.0001N NaOH) 540nm ( 3,450). IR: max (Nujol) 1708s, 1693s, 1677m, 1648m, 1632m, 1606s, 1566s, 1509 cm-1. Periodate oxidation is complete after 4hours at 0o with the consumption of 6.2 mols. The tetra-O-methyl carminate has m 186-188o (yellow needles from *C6H6/pet ether). [IR: Ali & Haynes J Chem Soc 1033 1959, Bhatia & Venkataraman Indian J Chem 3 (2) 92 1965, Synthesis: Davis & Smith Biochemical Preparations 4 38 1955, Beilstein 18 III/1V 6697.] |
| | Carminic Acid Preparation Products And Raw materials |
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