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(S)-Trolox methyl ether

for chiral derivatization, LiChropur, ≥98.0%

Synonym(s):

(S)-6-Methoxy-2,5,7,8-tetramethylchromane-2-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C15H20O4
CAS Number:
Molecular Weight:
264.32
Beilstein:
5481541
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.22

grade

for chiral derivatization

Quality Level

Assay

≥98.0% (sum of enantiomers, HPLC)
≥98.0%

form

powder

optical activity

[α]20/D −69±2°, c = 1% in ethanol

optical purity

enantiomeric ratio: ≥99.5:0.5 (HPLC)

quality

LiChropur

technique(s)

HPLC: suitable

mp

143-145 °C

SMILES string

COc1c(C)c(C)c2O[C@@](C)(CCc2c1C)C(O)=O

InChI

1S/C15H20O4/c1-8-9(2)13-11(10(3)12(8)18-5)6-7-15(4,19-13)14(16)17/h6-7H2,1-5H3,(H,16,17)/t15-/m0/s1

InChI key

MNBMVDGIDVXTOF-HNNXBMFYSA-N

General description

(S)-Trolox methyl ether is a chiral derivatizating agent, which is employed for derivatizing enantiomers into diastereoisomers.

Application

(S)-Trolox methyl ether may be used as a chiral derivatizing reagent for the following:        
  • analysis of chiral alcohols by capillary gas chromatography (GC) and supercritical fluid chromatography (SFC)       
  • enantiomeric separation of several benzodiazepines using gas chromatography (GC), supercritical fluid chromatography (SFC) and subcritical fluid chromatography techniques

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Chiral derivatizing agent for alcohols; some methyl substituted primary alcohols which are difficult to separate otherwise, can also be separated

Recommended products

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

W. Walther et al.
Chimia, 45, 121-121 (1991)
Design and development of chiral reagents for the chromatographic ee determination of chiral alcohols
Walther W and Netscher T
Chirality, 8(5), 397-401 (1996)
W. Walther et al.
J. Microcol. Sep., 4, 45-45 (1992)
Direct and indirect approaches to enantiomeric separation of benzodiazepines using micro column techniques
Almquist RS, et al.
Journal of Chromatography A, 679(1), 139-146 (1994)

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