Welcome to LookChem.com Sign In|Join Free
  • or
D-[1,6-13C2]FRUCTOSE is an isotope-labeled form of D-fructose, a monosaccharide that naturally occurs in a large number of fruits and plants. It is characterized by the presence of two 13C isotopes at the first and sixth carbon positions, which makes it a useful compound for various applications in scientific research and analysis.

287100-71-4

Post Buying Request

287100-71-4 Suppliers

Recommended suppliers

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

287100-71-4 Usage

Uses

Used in Scientific Research:
D-[1,6-13C2]FRUCTOSE is used as a research tool for studying metabolic pathways and enzyme mechanisms. The presence of 13C isotopes allows for the tracking of fructose metabolism in biological systems, providing valuable insights into the biochemical processes involving this sugar.
Used in Metabolic Studies:
In metabolic studies, D-[1,6-13C2]FRUCTOSE is used as a tracer compound to investigate the metabolic fate of fructose in living organisms. This helps researchers to understand the role of fructose in various metabolic pathways and its impact on health and disease.
Used in Analytical Chemistry:
D-[1,6-13C2]FRUCTOSE is used as an internal standard in analytical chemistry for the accurate quantification of fructose and other related compounds. The isotopic labeling provides a distinct signature that can be used to improve the precision and accuracy of analytical measurements.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, D-[1,6-13C2]FRUCTOSE can be used as a building block for the synthesis of isotopically labeled drug compounds. This allows for the investigation of drug metabolism and pharmacokinetics, as well as the development of new therapeutic agents with improved properties.
Used in Food Industry:
In the food industry, D-[1,6-13C2]FRUCTOSE may be used as a labeled ingredient to study the effects of fructose on food products and their nutritional profiles. This can help in the development of healthier food options and the understanding of the role of fructose in food science.

Check Digit Verification of cas no

The CAS Registry Mumber 287100-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,1,0 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 287100-71:
(8*2)+(7*8)+(6*7)+(5*1)+(4*0)+(3*0)+(2*7)+(1*1)=134
134 % 10 = 4
So 287100-71-4 is a valid CAS Registry Number.

287100-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4S)-2-(hydroxymethyl)oxane-2,3,4,5-tetrol

1.2 Other means of identification

Product number -
Other names D-Fructose-1,6-13C2

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:287100-71-4 SDS

287100-71-4Upstream product

287100-71-4Downstream Products

287100-71-4Relevant academic research and scientific papers

Integration of Enzymatic and Heterogeneous Catalysis for One-Pot Production of Fructose from Glucose

Sun, Jiankui,Li, Helong,Huang, Hongzhi,Wang, Bo,Xiao, Ling-Ping,Song, Guoyong

, p. 1157 - 1162 (2018/03/21)

The search for efficient routes for the production of fructose from biomass-derived glucose is of great interest and importance, as fructose is a highly attractive substrate in the conversion of cellulosic biomass into biofuels and chemicals. In this study, a one-pot, multistep procedure involving enzyme-catalyzed oxidation of glucose at C2 and Ni/C-catalyzed hydrogenation of d-glucosone at C1 selectively gives fructose in 77 % yield. Starting from upstream substrates such as α-cellulose and starch, fructose was also generated with similar efficiency and selectivity by the combination of enzymatic and heterogeneous catalysis. This method constitutes a new means of preparing fructose from biomass-derived substrates in an efficient fashion.

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 287100-71-4