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147990

Supelco

(R)-(−)-2-Octanol

for chiral derivatization, LiChropur, 99%

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About This Item

Linear Formula:
CH3(CH2)5CH(OH)CH3
CAS Number:
Molecular Weight:
130.23
Beilstein:
1719324
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.05

grade

for chiral derivatization

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

168.8 °F - closed cup

Flash Point(C)

76 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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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)
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Charlie Van Doorslaer et al.
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A methodology is introduced to separate polar reaction products from ionic liquids without the need for organic solvent extraction or distillation. We investigated product isolation after an alcohol oxidation performed in ionic liquids. Suitable ionic liquids were selected based on
Verónica Bisagno et al.
Psychopharmacology, 212(2), 205-214 (2010-07-24)
Repetitive cocaine exposure has been shown to induce GABAergic thalamic alterations. Given the key role of T-type (Ca(V)3) calcium channels in thalamocortical physiology, the direct involvement of these calcium channels in cocaine-mediated effects needs to be further explored. The objective

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