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Merck

77848

Supelco

(R)-(+)-1-苯基乙醇

for chiral derivatization, LiChropur, ≥99.0%

别名:

(+)-甲基苯基甲醇, (R)-(+)-α-甲基苯甲醇

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About This Item

经验公式(希尔记法):
C8H10O
CAS号:
分子量:
122.16
Beilstein:
2039798
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:
NACRES:
NA.05

等級

for chiral derivatization

品質等級

產品線

ChiraSelect

化驗

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

形狀

liquid

光學活性

[α]20/D +45±1°, c = 5% in methanol

光學純度

enantiomeric ratio: ≥99.5:0.5 (GC)

品質

LiChropur

技術

HPLC: suitable

折射率

n20/D 1.528

bp

88-89 °C/10 mmHg (lit.)

mp

9-11 °C (lit.)

密度

1.012 g/mL at 20 °C (lit.)

SMILES 字串

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 密鑰

WAPNOHKVXSQRPX-SSDOTTSWSA-N

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一般說明

(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.

其他說明

于检测对映体纯度和分离酸的手性试剂;环酐和环氧化物的不对称开环

推薦產品

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律資訊

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

儲存類別代碼

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

水污染物質分類(WGK)

WGK 3

閃點(°F)

185.0 °F - closed cup

閃點(°C)

85 °C - closed cup

個人防護裝備

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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