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147990

Supelco

(R)-(−)-2-Octanol

LiChropur, 99%

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About This Item

Linear Formula:
CH3(CH2)5CH(OH)CH3
CAS Number:
Molecular Weight:
130.23
Beilstein/REAXYS Number:
1719324
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.05

grade

derivatization grade ((chiral))

assay

99%

form

liquid

optical activity

[α]17/D −9.5°, neat

quality

LiChropur

technique(s)

HPLC: suitable

refractive index

n20/D 1.426 (lit.)

bp

175 °C (lit.)

density

0.820 g/mL at 20 °C (lit.)

SMILES string

CCCCCC[C@@H](C)O

InChI

1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3/t8-/m1/s1

InChI key

SJWFXCIHNDVPSH-MRVPVSSYSA-N

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General description

(R)-(−)-2-Octanol is a chiral derivatizating agent, which is employed for derivatizing enantiomers into diastereoisomers.

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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Timofey V Malyarenko et al.
Molecules (Basel, Switzerland), 23(5) (2018-05-13)
Two new polyhydroxysteroidal glycosides, anthenosides A₁ (1) and A₂ (2), and one previously known steroidal glycoside anthenoside A (3) were isolated from extract of the tropical starfish Anthenea aspera. Structures of 1⁻3 were determined by analysis of the spectroscopic data
Paul Masset et al.
Cell, 182(1), 112-126 (2020-06-07)
Every decision we make is accompanied by a sense of confidence about its likely outcome. This sense informs subsequent behavior, such as investing more-whether time, effort, or money-when reward is more certain. A neural representation of confidence should originate from
Xiao-Yang Ou et al.
Journal of biotechnology, 299, 37-43 (2019-05-03)
Highly efficient asymmetric reduction of 2-octanone to (R)-2-octanol catalyzed by immobilized Acetobacter sp. CCTCC M209061 cells was achieved in a biphasic system. Bioreduction conducted in aqueous single phase buffer was limited due to poor solubility and toxicity towards cells cause
G D Rees et al.
Biochimica et biophysica acta, 1073(3), 493-501 (1991-04-09)
Lipase from three different sources has been immobilised in microemulsion-based gels (MBGs) with retention of catalytic activity. Such lipase-containing MBGs prove to be novel solid-phase catalysts for use in apolar organic solvents such as n-heptane. Using these systems, preparative-scale synthesis
Chi-Yu Huang et al.
International journal of pharmaceutics, 325(1-2), 132-139 (2006-07-22)
Core-shell type of nanoparticles (NPs) with manipulated degradation rate and balanced hydrophilic/hydrophobic properties were designed and characterized. The NPs based on the copolymers of n-butyl cyanoacrylate (BCA) and 2-octyl cyanoacrylate (OCA) were prepared by anion emulsion polymerization in 0.01N HCl

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