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WIMWG10004SJ

Bruker® SampleJet NMR tubes with caps

L 103.5 mm, O.D. 5.0 mm, cap

Synonym(s):

nmr sample tubes, nmr tubes

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About This Item

UNSPSC Code:
41121705
NACRES:
SB.32

material

colorless tube

description

Wilmad tube with Bruker SampleJet caps

feature

cap
neck thread push fit

packaging

pack of 100 ea

manufacturer/tradename

Wilmad WG-1000-4-SJ

parameter

600 MHz frequency

L

103.5 mm

O.D.

5.0 mm

camber

60 μm

tube diam.

5 mm

wall thickness

0.43 mm

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General description

Wilmad Thin-Walled High Throughput NMR Tubes with authentic Bruker®SampleJet caps without code have an average camber of 60 microns to guarantee the SNR of the spectrum for small molecule (MW<250) samples up to 600 MHz. Do not use with ceramic spinners.
Wilmad NMR tubes with authentic Bruker® SampleJet caps without code, up to 600 MHz. Do not use with ceramic spinners.

Application

Bruker® SampleJet NMR tubes has been used as a sample holder in the NMR experiments.

Features and Benefits

  • Top-notch OD tolerances in the industry
  • Ensured tight fit in the spinner turbine
  • Designed for regular operation in most low to mid field NMR spectrometers
  • Catalog numbers ending in “-SJ” feature authentic Bruker SampleJet Caps

Legal Information

Bruker is a registered trademark of Bruker-Physik AG
SampleJet is a trademark of Bruker-Physik AG

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Young-Sang Jung et al.
Analytica chimica acta, 934, 194-202 (2016-08-11)
The goal of metabolomics is to analyze a whole metabolome under a given set of conditions, and accurate and reliable quantitation of metabolites is crucial. Absolute concentration is more valuable than relative concentration; however, the most commonly used method in
Nan Hee Kim et al.
Archives of biochemistry and biophysics, 646, 90-97 (2018-04-06)
Diabetic kidney disease (DKD) involves various pathogenic processes during progression to end stage renal disease, and activated metabolic pathways might be changing based on major pathophysiologic mechanisms as DKD progresses. In this study, nuclear magnetic resonance spectroscopy (NMR)-based metabolic profiling

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