beta-Citraurin

Base Information

Chemical Name:beta-Citraurin
CAS No.:650-69-1
Molecular Formula:C30H40O2
Molecular Weight:432.646
Hs Code.:
UNII:GRI2528DO7
DSSTox Substance ID:DTXSID201024326
Nikkaji Number:J7.072F
Wikidata:Q27123988
Metabolomics Workbench ID:58571
Mol file:650-69-1.mol

Synonyms:beta-citraurin;citraurin

Suppliers and Price of beta-Citraurin

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
BETA-CITRAURIN 95.00%
5MG
$ 495.86

Total 4 raw suppliers

Chemical Property of beta-Citraurin

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:147°
Refractive Index:1.5045 (estimate)
Boiling Point:609.402°C at 760 mmHg
Flash Point:253.885°C
PSA：37.30000
Density:0.992g/cm³
LogP:7.69270
XLogP3:8.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:9
Exact Mass:432.302830514
Heavy Atom Count:32
Complexity:922

Purity/Quality:

99% ^*data from raw suppliers

BETA-CITRAURIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C
Isomeric SMILES:CC1=C(C(C[C@@H](C1)O)(C)C)/C=C/C(=C/C=C/C(=C/C=C/C=C(\C)/C=C/C=C(\C)/C=O)/C)/C
Uses β-Citraurin is an antioxidant β-carotene (C184250) that is found in the peels and juices of oranges, pummelo, and grapefruit.

Technology Process of beta-Citraurin

There total 10 articles about beta-Citraurin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: (R)-4-((1E,3E,5E,7E,9E,11E,13E,15E)-17,17-Diethoxy-3,7,12,16-tetramethyl-heptadeca-1,3,5,7,9,11,13,15-octaenyl)-3,5,5-trimethyl-cyclohex-3-enol

: 650-69-1
(3R)-3-hydroxy-8'-apo-β-caroten-8'-al

Guidance literature:: With acetic acid; In water; Yield given;
DOI:10.1002/hlca.19800630604

Reference yield:

: 650-69-1
3-hydroxy-apo-8'-carotenal

Guidance literature:: With potassium hydroxide; at 80 ℃;

Reference yield:

: 54165-55-8
(3R)-3-Acetoxy-β-ionon

: 650-69-1
(3R)-3-hydroxy-8'-apo-β-caroten-8'-al

Guidance literature:: Multi-step reaction with 6 steps

1: 90 percent / KOH / methanol / 0.5 h

2: 1.) Mg / 1.) THF 2.) THF, 0 deg C, 30 min

3: methanol / 36 h / Ambient temperature

4: 70 percent / 2N NaOH / CH₂Cl₂; H₂O

5: Na / ethanol / Ambient temperature

6: AcOH / H₂O

With potassium hydroxide; sodium hydroxide; sodium; magnesium; acetic acid; In methanol; ethanol; dichloromethane; water;
DOI:10.1002/hlca.19800630604