psi,psi-Carotin

Lycopene Struktur
502-65-8
CAS-Nr.
502-65-8
Bezeichnung:
psi,psi-Carotin
Englisch Name:
Lycopene
Synonyma:
Lycopen;JARCOPENE(TM);LYCOSOURCE;Lycopene oil;Lycoypene;Lycopene Powder;E 160d;LYCOVIT;CI 75125;Y,Y-CAROTENE
CBNumber:
CB5213951
Summenformel:
C40H56
Molgewicht:
536.87
MOL-Datei:
502-65-8.mol

psi,psi-Carotin Eigenschaften

Schmelzpunkt:
172-173°C
Siedepunkt:
644.94°C (rough estimate)
Dichte
0.9380 (estimate)
Brechungsindex
1.5630 (estimate)
FEMA 
4110 | TOMATO LYCOPENE
storage temp. 
-70°C
Löslichkeit
Benzene (Slightly), Chloroform (Sparingly), Ethyl Acetate (Very Slightly), Methane
Aggregatzustand
powder
Farbe
Red to Very Dark Red
Geruch (Odor)
balsam oriental
Geruchsart
balsamic
Stabilität:
Heat sensitive - store at -70 C. Combustible. Incompatible with strong oxidizing agents.
InChIKey
OAIJSZIZWZSQBC-BOJOQWLHSA-N
LogP
15.19
CAS Datenbank
502-65-8(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 36/37/38
S-Sätze: 26-36/37/39
WGK Germany  3
8-10-23
HS Code  32030019
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P302+P352 BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckmäßig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.

psi,psi-Carotin Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.

Beschreibung

Lycopene is a red-colored carotenoid found in tomatoes and other red fruits and vegetables. Carotenoids, including lycopene, are powerful antioxidants that efficiently quench singlet oxygen. Presumably through this action, carotenoids may protect against cancers, cardiovascular stress, and other diseases.

Chemische Eigenschaften

Lycopene is a white to pale-yellow solid; balsam oriental aroma. Lycopene extract from tomato is a dark-red viscous liquid. It is freely soluble in ethyl acetate and n-hexane, partially soluble in ethanol and acetone, and insoluble in water. A solution in n-hexane shows an absorption maximum at approximately 472nm.
Lycopene (from the Greek word lykopersikon, meaning tomato) is a bright red carotene and carotenoid pigment. The natural resources are red fruits and vegetables, such as tomatoes, pink grapefruit, watermelon, and apricots. After absorbing from the stomach, lycopene is transported in the blood and accumulates in the liver, adrenal glands, and testes. Lycopene has been used to prevent carcinogenesis, cardiovascular diseases and aging.
Lycopene
From a chemistry perspective, lycopene is a symmetrical tetraterpene assembled from 8 isoprene units, containing 11 conjugated and 2 non-conjugated double bonds between carbon atoms. Lycopene is a member of the carotenoid family, and the predominant source in the human diet comes from tomato and tomato-based products. The antioxidant capacity of tomato strongly depends on the content and bioavailability of lycopene in the fruit. There is strong correlation between lycopene content in tomatoes and antioxidant capacity.

Occurrence

Lycopene is a carotenoid that occurs naturally in tomatoes.

Verwenden

Lycopene extract from tomato is intended for use as a food colour. It provides the similar colour shades, ranging from yellow to red, as do the natural and synthetic lycopenes. Lycopene extract from tomato is also used as a food/dietary supplement in products where the presence of lycopene provides a specific value (e.g., antioxidant or other claimed health benefits). The product may also be used as an antioxidant in food supplements.
Lycopene extract from tomato is intended for use in the following food categories: baked goods, breakfast cereals, dairy products including frozen dairy desserts, dairy product analogues, spreads, bottled water, carbonated beverages, fruit and vegetable juices, soybean beverages, candy, soups, salad dressings, and other foods and beverages.

Vorbereitung Methode

Lycopene extract from tomato is produced from a tomato variety with high lycopene content, within the range of 150 to 250 mg/kg. This particular variety is not generally marketed for direct consumption, but is used primarily in the production of this lycopene extract. The extract is produced by crushing tomatoes into crude tomato juice that is then separated into serum and pulp. The tomato pulp is then extracted with ethyl acetate. The final product is obtained after solvent removal by evaporation under vacuum at 40-60°C.

Definition

ChEBI: An acyclic carotene commonly obtained from tomatoes and other red fruits.

Allgemeine Beschreibung

Lycopene is a naturally occurring red pigment, which belongs to the family of carotenoids. It is found in tomatoes, watermelon and papaya. Lycopene has antioxidant property.

Biologische Aktivität

Lycopene may act as an inhibitor of tumor cells. In one study, lycopene was shown to inhibit PDGF-BB-induced signalling and cell migration in human cultured skin fibroblasts (Wu et al., 2007). Trapping of PDGF by lycopene compromised melanoma-induced fibroblast migration and attenuated signalling transduction in fibroblasts (Wu et al., 2007). In functional studies, lycopene inhibited melanoma-induced fibroblast migration in a noncontact coculture system and attenuated signalling in fibroblasts simulated by melanoma-derived conditioned medium (Chiang et al., 2007).

Mechanism of action

Lycopene is a red carotenoid compound found in pink grapefruit, papaya, wolfberry, goji, and tomatoes Dietary supplementation with tomato-based products appears to lower biomarkers of oxidative stress and carcinogenesis. Limited available evidence from small human intervention studies indicate that lycopene supplementation for 10–12 weeks may decrease UV-induced erythema. Although the bioavailability of lycopene in raw tomatoes is low due to tight binding with indigestible fiber, lycopene can be released from the food matrix through heating and food processing. The effect of topical lycopene is not well characterized. An in vivo study using SKH-1 hairless mice found that topical lycopene reduced the activity of ornithine decarboxylase (ODC) and myeloperoxidase (MPO), enzymes that have been implicated in the carcinogenic and acute inflammatory effect of UVB irradiation.

Anticancer Research

Lycopene is a naturally occurring chemical that manifests as a red pigment contained in common foods such as tomatoes, pink grapefruits, guava, and watermelon (Giovannucci 1999). This is a very strong antioxidant that has been found to prevent and even reverse the progression of prostate cancer, as well as treating benign prostatic hyperplasia. In a recent study, 30 mg a day of lycopene showed curative results in prostate cancer. For best results, supplements are recommended alongside eating and drinking plenty of lycopene-containing food and juices (Jatoi et al. 2007). Earlier research showed that taking a specific combination of lycopene, selenium, and saw palmetto by mouth for 8 weeks reduced pain in men with prostate swelling and pelvic pain more significantly than saw palmetto alone (Feifer et al. 2002).Lycopene shows anticancer activity against prostate, endometrial, breast, and colon carcinomas. It inhibits human cancer cell proliferation by activation of cancer-preventive enzymes like phase II detoxification enzymes, by suppression of insulin-like growth factor-I-stimulated growth (Wang et al. 2012). It also activates antioxidant enzymes like GST, GSH, and GPx and protects from oxidative stress caused by carcinogens. It alters PI3K/AKT pathway and ERK and Bcl-2 signaling in pancreatic and gastric carcinoma cells, respectively (Singh et al. 2016b).

läuterung methode

Crystallise lycopene from CS2/MeOH, diethyl ether/pet ether, or acetone/pet ether. Also purify it by column chromatography on deactivated alumina, CaCO3, calcium hydroxide or magnesia. It is oxygen sensitive and is stored in the dark, in an inert atmosphere. Also purified like -Carotene. [Beilstein 1 III 1076, 1 IV 1165.]

psi,psi-Carotin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


psi,psi-Carotin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 616)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Changsha Staherb Natural Ingredients Co., Ltd.
+86-0731-84213302 +8618374838656
sales@staherb.cn China 1025 58
XI AN SGONEK BIOLOGICAL TECHNOLOGY CO., LTD
15202951039
jason@sgonekbio.com China 268 58
Hangzhou Zelixir Biotech Co., Ltd.
+8618867646786
neal.chen@zelixir.com China 230 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12471 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118
xie@china-sinoway.com China 992 58
Henan Bao Enluo International TradeCo.,LTD
+86-17331933971 +86-17331933971
deasea125996@gmail.com China 2503 58
Hebei Kingfiner Technology Development Co.Ltd
+86-15532196582 +86-15373005021
lisa@kingfinertech.com China 3001 58
Hebei Jingbo New Material Technology Co., Ltd
+8619931165850
hbjbtech@163.com China 1000 58
Chongqing Zhihe Biopharmaceutical Co., Ltd.
+86-18580541567 +86-17782035140
sales@zhswyy.com China 242 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652
info@fdachem.com China 18229 58

502-65-8(psi,psi-Carotin)Verwandte Suche:


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  • Redivivo (Lycopene) 10% CWS/S-TG
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  • LYCOPENE (NATURAL YELLOW 27)
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  • Lycopin
  • (6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
  • LYCOPENE SNAP-N-SHOOT 0.1mg/mL(P)
  • LYCOPENE10CWD
  • LYCOPENE(SYNTHETIC)
  • FORMULATEDLYCOPENE
  • TRANS-LYCOPENE
  • SYNTHETICCRYSTALLINELYCOPENE
  • ALL-TRANS-LYCOPENE
  • 2,6,10,14,19,23,27,31-Octamethyl-dotriacont2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
  • ω,ω-Carotene, 2,6,10,14,19,23,27,31-Octamethyl-dotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
  • (6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-Octamethyldotriacontane-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
  • LyocpenePowder
  • Lycopene,ψ,ψ-Carotene, 2,6,10,14,19,23,27,31-Octamethyl-dotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
  • 4,4-CAROTENE
  • Nano Liposomal lycopene from tomato
  • The tomato extracts
  • Lycopene 502-65-8
  • (all-E)-2,6,10,14,19,23,27,31-Octamethyl-2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene
  • Soluble LYCOPENE, Liposomal LYCOPENE, LYCOPENE NanoEmulsion, NanoActive LYCOPENE
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  • Lycopene, Redivivo(TM)
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  • LYCOPENE EXTRACT 10%
  • LYCOPENE/CAS:502-65-8
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  • JARCOPENE(TM)
  • Y,Y-CAROTENE
  • E 160d
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  • Lycopene Powder
  • Lycoypene
  • lycopene from tomato
  • CI 75125
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