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Merck
CN

69808

Mineral oil

suitable for IR spectroscopy

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About This Item

CAS Number:
UNSPSC Code:
12352100
EC Number:
232-455-8
MDL number:
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InChI key

AEOVEGJBKQQFOP-DDVLFWKVSA-L

technique(s)

IR spectroscopy: suitable

refractive index

n20/D 1.467 (lit.), n20/D 1.468

density

0.85 g/mL at 20 °C

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Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves

Regulatory Information

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Takeshi Itabashi et al.
Nature methods, 6(2), 167-172 (2009-01-20)
Accurate chromosome segregation during meiosis depends on the assembly of a microtubule-based spindle of proper shape and size. Current models for spindle-size control focus on reaction diffusion-based chemical regulation and balance in activities of motor proteins. Although several molecular perturbations
Xuchu Ma et al.
Dalton transactions (Cambridge, England : 2003), (46)(46), 10250-10255 (2009-11-19)
Na(4)Si(4) and Na(4)Ge(4) are ideal chemical precursors for inorganic clathrate structures, clusters, and nanocrystals. The monoclinic Zintl phases, Na(4)Si(4) and Na(4)Ge(4), contain isolated homo-tetrahedranide [Si(4)](4-) and [Ge(4)](4-) clusters surrounded by alkali metal cations. In this study, a simple scalable route
Angela Rouyar et al.
PloS one, 6(10), e26443-e26443 (2011-10-27)
In nature the aerial trace of pheromone used by male moths to find a female appears as a train of discontinuous pulses separated by gaps among a complex odorant background constituted of plant volatiles. We investigated the effect of such
Benjamin Grau et al.
Purinergic signalling, 4(4), 357-364 (2008-09-09)
The formation of appropriate connections between neurons and their specific targets is an essential step during development and repair of the nervous system. Growth cones are located at the leading edges of the growing neurites and respond to environmental cues
Marie-Laure Volvert et al.
BMC pharmacology, 8, 10-10 (2008-06-14)
Lipid-soluble thiamine precursors have a much higher bioavailability than genuine thiamine and therefore are more suitable for therapeutic purposes. Benfotiamine (S-benzoylthiamine O-monophosphate), an amphiphilic S-acyl thiamine derivative, prevents the progression of diabetic complications, probably by increasing tissue levels of thiamine

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