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BAF371250078

Spinfin® magnetic stirring bar

H × diam. 0.5 in. (12.7 mm) × 0.875 in. (22.2 mm)

Synonym(s):

Spinfin® magnetic stirring bar

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About This Item

UNSPSC Code:
41122800
NACRES:
NB.51

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material

PTFE-coated

packaging

pack of 1 ea

manufacturer/tradename

Bel-Art F37125-0078

H × diam.

0.5 in. (12.7 mm) × 0.875 in. (22.2 mm)

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1 of 4

This Item
D5899D6134D3179
assay

≥99.0% (TLC)

assay

≥99% (GC)

assay

≥99% (GC)

assay

≥98% (GC)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

solubility

water: 100 mg/mL, clear to slightly hazy, colorless to light yellow

solubility

H2O: soluble 330 mg/mL, clear, colorless

solubility

H2O: 1 M at 20 °C, clear, colorless

form

solid

form

powder

form

crystalline

form

powder

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

impurities

<0.5% Sulphated ash

impurities

-

impurities

-

impurities

≤0.001% Phosphorus (P), <0.1% Insoluble matter

General description

Disks have fins on top for complete agitation.
Spinfin® magnetic stirring bars agitate liquids in round bottom vessels such as test tubes, cylinders and flasks, where other stirring bars cannot be used.

Features and Benefits

  • Maintains its position in a vessel and will not wobble
  • Alnico magnet encapsulated in FDA Grade, USP Class VI PTFE coating – Superior Chemical Compatibility
  • Manufactured in a registered ISO 9001:2015 facility, as verified by SGS certification
  • Autoclave safe

Legal Information

Spinfin is a registered trademark of SP Scienceware, a division of SP

Regulatory Information

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Xican Li
Food chemistry, 141(3), 2083-2088 (2013-07-23)
The deoxyribose degradation assay is widely used to evaluate the hydroxyl (OH) radical-scavenging ability of food or medicines. We compared the hydroxyl radical-scavenging activity of 25 antioxidant samples prepared in ethanol solution with samples prepared after removing the ethanol (residue).
Marina Rossi et al.
Physical review letters, 110(10), 107801-107801 (2013-03-26)
Concentrated solutions of ultrashort duplex-forming DNA oligomers may develop various forms of liquid crystal ordering among which is the chiral nematic phase, characterized by a macroscopic helical precession of molecular orientation. The specifics of how chirality propagates from the molecular
Jean Cadet et al.
Free radical research, 46(4), 367-381 (2012-01-24)
A broad scientific community is involved in investigations aimed at delineating the mechanisms of formation and cellular processing of oxidatively generated damage to nucleic acids. Perhaps as a consequence of this breadth of research expertise, there are nomenclature problems for
Katarzyna Lamparska et al.
Nucleic acids research, 40(19), 9788-9801 (2012-08-02)
5-Aza-2'-deoxycytidine (5azaC-dR) has been employed as an inhibitor of DNA methylation, a chemotherapeutic agent, a clastogen, a mutagen, an inducer of fragile sites and a carcinogen. However, its effects are difficult to quantify because it rapidly breaks down in aqueous
Guillaume Mata et al.
The Journal of organic chemistry, 77(20), 9006-9017 (2012-09-15)
An efficient method for the N-2-deoxyribosylation of modified nucleobases by 2-deoxythioriboside donors is reported. In the presence of an in situ silylated nucleobase, thioglycosides can be activated with NIS/HOTf to give nucleosides in high yields and with good β-selectivity. By

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