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Merck
모든 사진(1)

문서

77879

Supelco

(R)-(+)-α-Methylbenzylamine

for chiral derivatization, LiChropur, ≥99.0%

동의어(들):

(R)-(+)-1-Phenylethylamine

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About This Item

Linear Formula:
C6H5CH(CH3)NH2
CAS Number:
Molecular Weight:
121.18
Beilstein:
2410916
EC Number:
MDL number:
UNSPSC 코드:
12000000
PubChem Substance ID:
NACRES:
NA.22

Grade

for chiral derivatization

Quality Level

vapor pressure

0.5 mmHg ( 20 °C)

분석

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

형태

liquid

광학 활성

[α]20/D +30±1°, c = 10% in ethanol

광학 순도

enantiomeric ratio: ≥99.5:0.5 (GC)

품질

LiChropur

기술

HPLC: suitable

refractive index

n20/D 1.526 (lit.)
n20/D 1.528

bp

187-189 °C (lit.)

density

0.952 g/mL at 20 °C (lit.)

저장 온도

2-8°C

SMILES string

C[C@@H](N)c1ccccc1

InChI

1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m1/s1

InChI key

RQEUFEKYXDPUSK-SSDOTTSWSA-N

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일반 설명

(R)-(+)-α-Methylbenzylamine is a high quality, useful chiral derivatization reagent for all analytical applications, specific to GC in the chiral field. It is specially selected to meet the requirements for derivatization reagents for enantiomeric excess determinations.

애플리케이션

(R)-(+)-a-Methylbenzylamine also known as (R)-(+)-1-Phenylethylamine may be used in resolution of a chiral arylalkylamine involving high-conversion enantioselective condensation with capric acid followed by hydrolysis to yield corresponding (R)-(+)-amide.

기타 정보

Chiral amine used for the determination of the enantiomeric purity of acids

추천 제품

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

법적 정보

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

픽토그램

CorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point (°F)

158.0 °F - closed cup

Flash Point (°C)

70 °C - closed cup

개인 보호 장비

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


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문서 라이브러리 방문

R.W. Souter
Chromatographic Separations of Stereoisomers null
W.H. Pirkle and J. Finn et al.
Asymmetric Synthesis, 1 (1983)
Easy-on, easy-off?resolution of chiral 1-phenylethylamine catalyzed by Candida antarctica lipase B.
Torres-Gavilan, A., et al.
Tetrahedron Asymmetry, 18.22, 2621-2624 (2007)
Bartosz Lewandowski et al.
Chemical communications (Cambridge, England), (47)(47), 6399-6401 (2008-12-03)
Simple chiral aza-crown ethers based on sucrose display high enantioselectivity in complexation of phenylethylammonium chlorides.
Paul E Harrington et al.
Current medicinal chemistry, 14(28), 3027-3034 (2008-01-29)
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