Croceic acid

Modify Date: 2024-01-02 23:53:39

Croceic acid Structure
Croceic acid structure
Common Name Croceic acid
CAS Number 27876-94-4 Molecular Weight 328.402
Density 1.1±0.1 g/cm3 Boiling Point 585.1±23.0 °C at 760 mmHg
Molecular Formula C20H24O4 Melting Point 285°
MSDS N/A Flash Point 321.7±19.1 °C

 Use of Croceic acid


Transcrocetin (trans-Crocetin), extracted from saffron (Crocus sativus L.), acts as an NMDA receptor antagonist with high affinity.

 Names

Name Crocetin
Synonym More Synonyms

 Croceic acid Biological Activity

Description Transcrocetin (trans-Crocetin), extracted from saffron (Crocus sativus L.), acts as an NMDA receptor antagonist with high affinity.
Related Catalog
Target

NMDA receptor[1]

In Vitro Transcrocetin (trans-Crocetin), a saffron metabolite originating from the crocin apocarotenoids, has been shown to exert strong NMDA receptor affinity and is thought to be responsible for the CNS activity of saffron.To ensure unchanged viability of Caco-2 cells throughout the transport experiments, cellular mitochondrial dehydrogenase activity of Caco-2 cells is measured by MTT assay after a 24 h incubation period with the test compounds: Hydroalcoholic saffron extract saffron extract (SE, 0.5-1 mg/mL) and crocin-1 (250-1000 µM) reveal no negative significant changes in cellular viability. Transcrocetin at 10 µM level does not change viability while higher concentrations (40-160 µM) reduces significantly cellular viability[1].
Cell Assay Cytotoxicity of test compounds is determined by MTT assay using Caco-2 cells in 96 well plates at a density of 20.000 cells per well in 200 µl FBS-free medium, grown for 96 h and followed by 24 h contact time with the test compounds (100 µL of serum-free media containing SE 0.5, 1, and 2 mg/mL; trans-crocin-1 250, 500, and 1000 µM; Transcrocetin 10, 40, 80, and 160 µM) and incubation at 37°C/5% CO2. The incubation solutions are aspirated, each well is washed twice with 150 µL of PBS and 50 µL of MTT solution are added (2.5 mg/mL in PBS). Supernatants are discarded and the formed formazan is dissolved in 50 µL of DMSO. The absorption of the resulting solution is determined at λ=492 nm against reference wavelength λ=690 nm[1].
References

[1]. Lautenschläger M, et al. Intestinal formation of trans-Crocetin from saffron extract (Crocus sativus L.) and in vitro permeation through intestinal and blood brain barrier. Phytomedicine. 2015 Jan 15;22(1):36-44.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 585.1±23.0 °C at 760 mmHg
Melting Point 285°
Molecular Formula C20H24O4
Molecular Weight 328.402
Flash Point 321.7±19.1 °C
Exact Mass 328.167450
PSA 74.60000
LogP 4.72
Vapour Pressure 0.0±3.5 mmHg at 25°C
Index of Refraction 1.559
Storage condition -20℃

 Synthetic Route

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Croceic acid Structure

Croceic acid

CAS#:27876-94-4

Literature: RIKEN VITAMIN CO., LTD. Patent: WO2004/78695 A1, 2004 ; Location in patent: Page 16 ;

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Croceic acid Structure

Croceic acid

CAS#:27876-94-4

Literature: Schwieter,U. et al. Helvetica Chimica Acta, 1971 , vol. 54, p. 2447 - 2459

 Synonyms

8,8'-Diapo-y,y-carotenedioic Acid
transcrocetin
2,4,6,8,10,12,14-Hexadecaheptaenedioic acid, 2,6,11,15-tetramethyl-, (2E,4E,6E,8E,10E,12E,14E)-
trans-Crocetin
carotenoid dicarboxylic acid
(2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethyl-2,4,6,8,10,12,14-hexadecaheptaenedioic acid
8,8'-Diapocarotene-8,8'-dioic acid
all-trans-8,8'-diapocarotene-8,8'-dioic acid
Crocetin
Natural yellow 6
(2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-Tetramethylhexadeca-2,4,6,8,10,12,14-heptaenedioic acid
8,8'-Diapo-8,8'-carotenedioic acid
8,8'-Diapocarotenedioic acid
EINECS 248-708-0
FEMA 2998
Top Suppliers:I want be here
  • BioBioPha
  • China
  • Product Name: Crocetin
  • Price: ¥500.0/5mg
  • Purity: 98.0%
  • Stocking Period: 1 Day
  • Contact: Xueping-Zheng




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Price: ¥1200/5 mg

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