S0625

D-(−)-Salicin

≥99% (GC)

Manufacturer: Sigma Aldrich

CAS Number: 138-52-3

Synonym(S): 2-(Hydroxymethyl)phenyl-β-D-glucopyranoside, Salicoside, Salicyl alcohol glucoside, Saligenin β-D-glucoside

Select a Size

Pack Size SKU Availability Price
5 G S0625-5-G In Stock ₹ 2,836.15
25 G S0625-25-G In Stock ₹ 8,952.28
100 G S0625-100-G In Stock ₹ 44,599.00

S0625 - 5 G

₹ 2,836.15

In Stock

Quantity

1

Base Price: ₹ 2,836.15

GST (18%): ₹ 510.507

Total Price: ₹ 3,346.657

Quality Level

200

Assay

≥99% (GC)

form

powder

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

SMILES string

OC[C@H]1O[C@@H](Oc2ccccc2CO)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2/t9-,10-,11+,12-,13-/m1/s1

InChI key

NGFMICBWJRZIBI-UJPOAAIJSA-N

Other Options

Image Product Name Manufacturer Price Range
50-188-2494
Sigma Aldrich Fine Chemicals Biosciences D-(-)-Salicin >=99% (GC) | 138-52-3 | MFCD00006590 | 100G
Sigma Aldrich Fine Chemicals Biosciences ₹ 68,653.34
11-101-3027
D-(-)-Salicin, ≥98.5% (HPLC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 23,956.80
50-188-2496
Sigma Aldrich Fine Chemicals Biosciences D-(-)-Salicin >=99% (GC) | 138-52-3 | MFCD00006590 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 6,562.45
50-536-7
Selleck Chemical LLC Salicin 500mg 138-52-3 Salicoside,Salicine
Selleck Chemical LLC ₹ 8,111.09
79588
D-(−)-Salicin
Supelco ₹ 19,214.38
1607903
D-Salicin
Sigma Aldrich ₹ 35,311.15
PHL89782
Salicin
Sigma Aldrich ₹ 28,047.58
CS-8027
Salicin
ChemScene ₹ 2,566.80 - ₹ 4,278.00

Description

  • General description: Salicin is a non-phenolic glucosidic compound[1] extracted from meadowsweet (Filipendula ulmaria L). It is majorly used as a substitute for quinine. Salicin can be used as a therapeutic for patients suffering from rheumatic fever.[2] Salicin acts a metabolic precursor for salicylic acid.[3] It is a novel phytochemical that exhibits immunological cross functions in plants and humans. Salicin facilitates growth and reproduction in plants. In addition, It also protects plants against biotic and abiotic stress.[4]
  • Application: D-(-)-Salicin has been used:to study its in vitro anticoagulant and antiplatelet activities[1]as a standard in high performance liquid chromatography method (HPLC) for quantitation of salicin from willow plant[3][5]as a tastant in taste threshold assay[6]as a constituent of nutrient agar-salicin medium for selective isolation of Lactobacillus paracasei[7]
  • Biochem/physiol Actions: D-(−)-Salicin exerts anti-rheumatism and anti-inflammatory activities.[8] It inhibits lipopolysaccharide (LPS) induced inflammation in in vitro and in vivo studies.[8] It regulates different signaling pathways such as nuclear factor kappa B (NF-κB) and mitogen-activated protein kinase (MAPK).[8] It also regulates cytokines concentration such as tumor necrosis factor-alpha(TNF-α), interleukin-1β, interleukin-6, and interleukin-10.[8]

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H317

Precautionary Statements

P280 - P302 + P352

Hazard Classifications

Skin Sens. 1

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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≥99% (GC)

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metabolomicsvitamins, nutraceuticals, and natural products

SMILES string:
OC[C@H]1O[C@@H](Oc2ccccc2CO)[C@H](O)[C@@H](O)[C@@H]1O

InChI:
1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2/t9-,10-,11+,12-,13-/m1/s1

InChI key:
NGFMICBWJRZIBI-UJPOAAIJSA-N

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