CAS 55750-85-1
:Crocin 3
Description:
Crocin 3, with the CAS number 55750-85-1, is a carotenoid compound primarily derived from saffron, the dried stigma of the Crocus sativus flower. It is known for its vibrant yellow-orange color, which is attributed to its chemical structure that includes a series of conjugated double bonds. Crocin 3 exhibits antioxidant properties, making it of interest in various fields, including food science and pharmacology. It is soluble in organic solvents but has limited solubility in water, which can affect its bioavailability. The compound is often studied for its potential health benefits, including anti-inflammatory and neuroprotective effects. Additionally, crocin compounds are used as natural colorants in food products and cosmetics due to their stability and safety profile. Overall, Crocin 3 is a significant compound in both culinary and medicinal contexts, reflecting the broader importance of carotenoids in human health and nutrition.
Formula:C32H44O14
InChI:InChI=1S/C32H44O14/c1-17(11-7-13-19(3)29(40)41)9-5-6-10-18(2)12-8-14-20(4)30(42)46-32-28(39)26(37)24(35)22(45-32)16-43-31-27(38)25(36)23(34)21(15-33)44-31/h5-14,21-28,31-39H,15-16H2,1-4H3,(H,40,41)/b6-5+,11-7+,12-8+,17-9+,18-10+,19-13+,20-14+/t21-,22-,23-,24-,25+,26+,27-,28-,31-,32+/m1/s1
InChI key:InChIKey=VULLCGFNYWDRHL-YJOFKXFJSA-N
SMILES:C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H]2O[C@@H](OC(/C(=C/C=C/C(=C/C=C/C=C(/C=C/C=C(/C(O)=O)\C)\C)/C)/C)=O)[C@H](O)[C@@H](O)[C@@H]2O
Synonyms:- 8,8'-Diapo-y,y-carotenedioic acid, mono(6-O-b-D-glucopyranosyl-b-D-glucopyranosyl) ester
- 8,8′-Diapo-ψ,ψ-carotenedioic acid, mono(6-O-β-<span class="text-smallcaps">D</smallcap>-glucopyranosyl-β-<smallcap>D</span>-glucopyranosyl) ester
- Crocetin b-D-gentiobiosyl ester
- Crocetin gentiobiosyl ester
- Crocetin mono-b-D-gentiobiosyl ester
- Crocetin mono-β-<span class="text-smallcaps">D</span>-gentiobiosyl ester
- Crocetin monogentiobiosyl ester
- Crocetin β-<span class="text-smallcaps">D</span>-gentiobiosyl ester
- Crocin 3
- Crocin C
- Trans-crocin-3
- b-D-Glucopyranose, 1-O-(15-carboxy-2,6,11-trimethyl-1-oxo-2,4,6,8,10,12,14-hexadecaheptaenyl)-6-O-b-D-glucopyranosyl-, (all-E)-
- trans-Crocetin b-D-gentiobiosylester
- trans-Crocetin β-<span class="text-smallcaps">D</span>-gentiobiosyl ester
- β-<span class="text-smallcaps">D</smallcap>-Glucopyranose, 1-O-(15-carboxy-2,6,11-trimethyl-1-oxo-2,4,6,8,10,12,14-hexadecaheptaenyl)-6-O-β-<smallcap>D</span>-glucopyranosyl-, (all-E)-
- β-<span class="text-smallcaps">D</smallcap>-Glucopyranose, 6-O-β-<smallcap>D</span>-glucopyranosyl-, 1-[hydrogen (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-tetramethyl-2,4,6,8,10,12,14-hexadecaheptaenedioate]
- β-D-Glucopyranose, 6-O-β-D-glucopyranosyl-, 1-[hydrogen (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-tetramethyl-2,4,6,8,10,12,14-hexadecaheptaenedioate]
- 8,8′-Diapo-ψ,ψ-carotenedioic acid, mono(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl) ester
- (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptaenedioic acid 16-(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl) ester
- trans-Crocetin (β-D-gentiobiosyl) ester
- 8,8'-Diapo-ψ,ψ-carotene-8,8'-dioic acid 8-(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl) ester
- See more synonyms
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Found 6 products.
Crocin III
CAS:Formula:C32H44O14Purity:≥ 98.0%Color and Shape:Light yellow to orange powder or solidMolecular weight:652.69Crocin III
CAS:Crocin III (Crocetin-mono-(β-D-gentiobiosyl)-ester) is a crocin derived from saffron (Crocus sutivus L.).Formula:C32H44O14Purity:99.24%Color and Shape:SolidMolecular weight:652.68Crocin 3
CAS:Natural glycosideFormula:C32H44O14Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:652.68Beta-D-gentiobiosyl crocetin
CAS:<p>Beta-D-gentiobiosyl crocetin is a carotenoid glycoside, which is a natural compound derived from the saffron crocus (Crocus sativus) or Gardenia jasminoides fruits. It possesses a distinct structure where crocetin is linked to a gentiobiose sugar moiety. This compound exhibits its function primarily as an antioxidant by scavenging free radicals and inhibiting oxidative stress mechanisms. Such activity is mediated through the stabilization of cell membranes and the suppression of lipid peroxidation.</p>Formula:C32H44O14Purity:Min. 95%Molecular weight:652.7 g/mol





