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478518-83-1

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478518-83-1 Usage

Properties

1. Stable isotope-labeled glucose derivative
2. Synthetic chemical compound
3. Used in metabolic studies and stable isotope labeling experiments
4. Contains a stable carbon isotope
5. Useful for tracing metabolic pathways
6. Commonly used as a tracer in isotope dilution mass spectrometry and nuclear magnetic resonance spectroscopy
7. Valuable in understanding metabolic pathways

Specific content

1. Name: 2-ACETAMIDO-2-DEOXY-D-[UL-13C6]GLUCOSE
2. Type: Synthetic chemical compound
3. Use: Metabolic studies and stable isotope labeling experiments in biochemistry and medical research
4. Stable isotope: Carbon
5. Application: Tracing metabolic pathways and studying glucose metabolism in biological systems
6. Tracer in: Isotope dilution mass spectrometry and nuclear magnetic resonance spectroscopy
7. Value: Understanding metabolic pathways and studying glucose metabolism in health and disease states.

Check Digit Verification of cas no

The CAS Registry Mumber 478518-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,5,1 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 478518-83:
(8*4)+(7*7)+(6*8)+(5*5)+(4*1)+(3*8)+(2*8)+(1*3)=201
201 % 10 = 1
So 478518-83-1 is a valid CAS Registry Number.

478518-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ACETAMIDO-2-DEOXY-D-[UL-13C6]GLUCOSE

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:478518-83-1 SDS

478518-83-1Relevant articles and documents

Simplified determination of the content and average degree of acetylation of chitin in crude black soldier fly larvae samples

D'Hondt, Els,Soetemans, Lise,Bastiaens, Leen,Maesen, Miranda,Jespers, Vincent,Van den Bosch, Bert,Voorspoels, Stefan,Elst, Kathy

supporting information, (2020/01/25)

Insects are considered a promising alternative protein source for food and feed, but contain significant amounts of chitin, often undesirable due to indigestibility, disagreeable texture and negative effect on nutrients intake. Fractionation strategies are thus increasingly being applied to isolate and valorize chitin separately. The analysis of chitin generally requires an intensive pretreatment to remove impurities, and derivatization to generate sufficient detector response. In this work, a liquid chromatography method, without pretreatment nor derivatization, was developed for the simultaneous determination of chitin content and degree of acetylation in non-purified samples of black soldier fly (BSF) larvae. The method is found to be more suitable, compared to traditional methods, for assessing high degrees of acetylation. For the first time, the degree of acetylation of BSF chitin (81 ± 2%) is reported. Additionally, the chitin content of BSF soft tissues is estimated at approximately 20% of the total chitin content (8.5 ± 0.1%).

Escherichia coli O106, a new member of a group of enteric bacteria sharing an O-polysaccharide backbone structure

Shashkov,Senchenkova,Naumenko,Kalinchuk,Perepelov,Knirel, Yu. A.

, p. 1538 - 1541 (2018/10/31)

O-Polysaccharides (O-antigens) of a number of genetically related Escherichia coli O-serogroups (O17, O44, O73, O77, and O106) and Salmonella enterica O:6,14 possess an identical main chain composed of d-GlcNAc and d-Man residues and differ from each other by the absence or presence of glucose side chains at various positions. Using two-dimensional NMR spectroscopy, we established the structure of the O-polysaccharide of E. coli O106 having two glucose side chains in a hexasaccharide repeating unit.

Pro-apoptotic activity of acylated triterpenoid saponins from the stem bark of Albizia chevalieri harms

Noté, Olivier Placide,Messi, Lin Marcellin,Mbing, Joséphine Ngo,Azouaou, Sarah Ali,Sarr, Mamadou,Guillaume, Dominique,Muller, Christian Dominique,Pegnyemb, Dieudonné Emmanuel,Lobstein, Annelise

, p. 95 - 101 (2017/10/05)

As a continuation of our interest in apoptosis-inducing triterpenoid saponins from Albizia genus, phytochemical investigation of the stem bark of Albizia chevalieri led to the isolation of three new oleanane-type saponins, named chevalierosides A–C (1–3). Their structures were established on the basis of extensive analysis of 1D and 2D NMR (1H-, 13C NMR, DEPT, COSY, TOCSY, ROESY, HSQC and HMBC) experiments, HRESIMS studies, and by chemical evidence. The pro-apoptotic effect of the three saponins was evaluated on two human cell lines (pancreatic carcinoma AsPC-1 and hematopoietic monocytic THP-1). Cytometric analyses showed that saponins 1–3 induced apoptosis of both human cell lines (AsPC-1 and THP-1) in a dose-dependent manner.

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