Welcome to LookChem.com Sign In|Join Free
  • or
Pistilbeside is a chemical compound predominantly found in the pistil of flowering plants, playing a vital role in the plant's reproductive process. It is instrumental in attracting pollen and facilitating fertilization, while also contributing to the unique floral aroma that lures pollinators such as bees and butterflies. Moreover, Pistilbeside may possess antimicrobial properties, safeguarding the reproductive organs of plants from infections, thereby ensuring the successful reproduction and survival of flowering plants.

58762-96-2

Post Buying Request

58762-96-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

58762-96-2 Usage

Uses

Used in Fragrance Industry:
Pistilbeside is used as a natural fragrance ingredient for its distinct aroma, which is appealing to pollinators and can be harnessed in creating perfumes and other scented products.
Used in Agricultural Applications:
Pistilbeside is used as a natural attractant in agriculture to encourage pollination by bees and butterflies, thereby improving the reproductive success and yield of crops.
Used in Cosmetics and Personal Care:
Pistilbeside is used as a natural component in cosmetics and personal care products for its pleasant scent and potential antimicrobial properties, contributing to product efficacy and consumer appeal.
Used in Pharmaceutical Research:
Pistilbeside is used in pharmaceutical research for its potential antimicrobial properties, with the aim of developing new treatments or preventative measures against infections, particularly in the context of plant reproductive organs.
Used in Environmental Conservation:
Pistilbeside is used in environmental conservation efforts to support pollinator populations by enhancing the natural appeal of plants, thereby promoting biodiversity and ecosystem health.

Check Digit Verification of cas no

The CAS Registry Mumber 58762-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,6 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58762-96:
(7*5)+(6*8)+(5*7)+(4*6)+(3*2)+(2*9)+(1*6)=172
172 % 10 = 2
So 58762-96-2 is a valid CAS Registry Number.

58762-96-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(E)-2-(3-Hydroxy-5-methoxyphenyl)vinyl]phenyl β-D-glucopyranos ide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58762-96-2 SDS

58762-96-2Relevant academic research and scientific papers

Synthesis, oxygen radical absorbance capacity, and tyrosinase inhibitory activity of glycosides of resveratrol, pterostilbene, and pinostilbene

Uesugi, Daisuke,Hamada, Hiroki,Shimoda, Kei,Kubota, Naoji,Ozaki, Shin-Ichi,Nagatani, Naoki

, p. 226 - 230 (2017)

The stilbene compound resveratrol was glycosylated to give its 4′-O-β-D-glucoside as the major product in addition to its 3-O-β-D-glucoside by a plant glucosyltransferase from Phytolacca americana expressed in recombinant Escherichia coli. This enzyme transformed pterostilbene to its 4′-O-β-D-glucoside, and converted pinostilbene to its 4′-O-β-D-glucoside as a major product and its 3-O-β-D-glucoside as a minor product. An analysis of antioxidant capacity showed that the above stilbene glycosides had lower oxygen radical absorbance capacity (ORAC) values than those of the corresponding stilbene aglycones. The 3-O-β-D-glucoside of resveratrol showed the highest ORAC value among the stilbene glycosides tested, and pinostilbene had the highest value among the stilbene compounds. The tyrosinase inhibitory activities of the stilbene aglycones were improved by glycosylation; the stilbene glycosides had higher activities than the stilbene aglycones. Resveratrol 3-O-β-D-glucoside had the highest tyrosinase inhibitory activity among the stilbene compounds tested.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 58762-96-2