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Merck
모든 사진(1)

문서

77848

Supelco

(R)-(+)-1-Phenylethanol

for chiral derivatization, LiChropur, ≥99.0%

동의어(들):

(+)-Methyl phenyl carbinol, (R)-(+)-α-Methylbenzyl alcohol

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About This Item

실험식(Hill 표기법):
C8H10O
CAS Number:
Molecular Weight:
122.16
Beilstein:
2039798
MDL number:
UNSPSC 코드:
12000000
PubChem Substance ID:
NACRES:
NA.05

Grade

for chiral derivatization

Quality Level

제품 라인

ChiraSelect

분석

≥99.0% (sum of enantiomers, GC)
≥99.0%

형태

liquid

광학 활성

[α]20/D +45±1°, c = 5% in methanol

광학 순도

enantiomeric ratio: ≥99.5:0.5 (GC)

품질

LiChropur

기술

HPLC: suitable

refractive index

n20/D 1.528

bp

88-89 °C/10 mmHg (lit.)

mp

9-11 °C (lit.)

density

1.012 g/mL at 20 °C (lit.)

SMILES string

C[C@@H](O)c1ccccc1

InChI

1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-/m1/s1

InChI key

WAPNOHKVXSQRPX-SSDOTTSWSA-N

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일반 설명

(R)-(+)-1-Phenylethanol is a chiral derivatizating agent, which is employed for derivatizing acids for their subsequent analysis using gas chromatography as the analytical technique.

기타 정보

Chiral reagent used for the determination of enantiomeric purity and for resolutions of acids; Asymmetric opening of cyclic anhydrides and of epoxides

추천 제품

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

법적 정보

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

185.0 °F - closed cup

Flash Point (°C)

85 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

Y. Takeuchi et al.
Journal of the Chemical Society. Perkin Transactions 1, 2203-2203 (1987)
S.V. Ley et al.
Tetrahedron, 46, 4995-4995 (1990)
T. Rosen et al.
Journal of the American Chemical Society, 107, 3731-3731 (1985)
H. Niwa et al.
Tetrahedron Letters, 29, 5139-5139 (1988)
Sachiko Sugimoto et al.
Phytochemistry, 108, 189-195 (2014-12-03)
Three aromatic glycosides (1-3), two sulfur and nitrogen-containing compound glucosides (4, 5), and one flavonoid glycoside (6) were isolated from the leaves of Ixora undulata. Their structures were established by extensive 1D, 2D NMR, and HRESIMS experiments, and structure 4

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