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S8754

Solanesol from tobacco

≥90% (HPLC)

Synonym(e):

Betulanonaprenol, Nonaisoprenol

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Über diesen Artikel

Empirische Formel (Hill-System):
C45H74O
CAS-Nummer:
Molekulargewicht:
631.07
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352212
MDL number:


Quality Segment

assay

≥90% (HPLC)

form

powder

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

C\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CO

InChI

1S/C45H74O/c1-37(2)19-11-20-38(3)21-12-22-39(4)23-13-24-40(5)25-14-26-41(6)27-15-28-42(7)29-16-30-43(8)31-17-32-44(9)33-18-34-45(10)35-36-46/h19,21,23,25,27,29,31,33,35,46H,11-18,20,22,24,26,28,30,32,34,36H2,1-10H3/b38-21+,39-23+,40-25+,41-27+,42-29+,43-31+,44-33+,45-35+

InChI key

AFPLNGZPBSKHHQ-MEGGAXOGSA-N

General description

Solanesol is mainly extracted from Nicotiana tabacum (tobacco).[1] It is an aliphatic terpene, polyisoprenoid alcohol.[1] Solanesol can also be found in other solanaceous plants such as tomato (Solanum lycopersicum), potato (Solanum tuberosum), eggplant, bell peppers.[1]This C45 isoprenoid alcohol is the most abundant lipid in tobacco leaves.

Application

Solanesol from tobacco has been used as a reference standard for the quantification of solanesol from different tobacco leaf samples using reverse-phase high-performance liquid chromatography (RP-HPLC).[2] It has also been used to increase the stability of artificial liposomes to test the mechanical function of ubiquinone-8 (Q8)-mediated membrane stabilization in E. coli under osmotic stress.[3]

Biochem/physiol Actions

Solanesol displays antioxidant, anti-inflammatory, neuroprotective, and antimicrobial activities.[1] It also exerts anti-cancer properties as a therapeutic carrier by binding together with thiosalicyclic acid (TS) and hyaluronic acid (HA).[4][5]Solanesol may be an important precursor of the tumorigenic polynuclear aromatic hydrocarbons of smoke.

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Dieser Artikel
91211W274711W249166
form

powder

form

solid

form

-

form

-

assay

≥90% (HPLC)

assay

≥97.0% (HPLC)

assay

≥98%

assay

≥95%

Quality Level

200

Quality Level

100

Quality Level

300

Quality Level

300

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

application(s)

flavors and fragrances

application(s)

flavors and fragrances

storage temp.

−20°C

storage temp.

-

storage temp.

2-8°C

storage temp.

2-8°C


Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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Study on supercritical fluid extraction of solanesol from industrial tobacco waste
Wang, Yu and Gu, Wenbo
Journal of Supercritical Fluids, 138, 228-237 (2018)
Jian-Hong Wang et al.
Journal of Asian natural products research, 11(11), 978-984 (2010-02-26)
Novel solanesylpiperazinotriamines as well as their N-aryl-substituted analogs were synthesized starting from solanesol through a multistep procedure. Their structures were confirmed by IR, (1)H NMR, MS, and elemental analysis. The preliminary results indicated that these novel derivatives were preferentially toxic
Jiangyong Hu et al.
Se pu = Chinese journal of chromatography, 25(4), 528-531 (2007-11-01)
Preparative high-speed counter-current chromatography (HSCCC) was used for the isolation and purification of solanesol from potato leaves. Experimental conditions of the extraction of solanesol from potato leaves have been optimized. An ultrafine extraction method was applied in this study. The



Global Trade Item Number

SKUGTIN
S8754-250MG04061833276136
S8754-25MG04061836961039

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