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576166

Sigma-Aldrich

1-(2-Hydroxyethyl)imidazole

97%

Sinónimos:

1-(β-Hydroxyethyl)imidazole, 1-(2-Hydroxyethyl)-1H-imidazole, 1-(2′-Hydroxyethyl)imidazole, 2-(1H-Imidazol-1-yl)ethan-1-ol, 2-(1H-Imidazol-1-yl)ethanol, 2-(1′-Imidazolyl)ethanol, 2-(Imidazol-1-yl)ethanol, N-(2-Hydroxyethyl)-1H-imidazole, N-(2-Hydroxyethyl)imidazole

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About This Item

Fórmula empírica (notación de Hill):
C5H8N2O
Número de CAS:
1615-14-1
Peso molecular:
112.13
EC Number:
216-565-3
MDL number:
MFCD00209980
UNSPSC Code:
12352005
PubChem Substance ID:
24880845
NACRES:
NA.22

assay

97%

form

solid

mp

36-40 °C (lit.)

functional group

hydroxyl

SMILES string

OCCn1ccnc1

InChI

1S/C5H8N2O/c8-4-3-7-2-1-6-5-7/h1-2,5,8H,3-4H2

InChI key

AMSDWLOANMAILF-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

>230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCT4480
MKCN8974
MKCK7543
MKCG3218
MKCB9970

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Sigma-Aldrich

666408

2-Chloro-1H-imidazole

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The online combination of capillary electrophoresis (CE) with mass spectrometry (MS) has long been desired for the capability of direct and simultaneous separation and detection with high efficiency, accuracy, and throughput. In this work, a novel CE-MS interface was developed
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Journal of chromatography. A, 1620, 461013-461013 (2020-03-24)
Dummy molecularly imprinted microspheres (DMIMs) were synthesized by Pickering emulsion polymerization and used as the matrix solid-phase dispersion extraction (MSPD) sorbent for sample pre-treatment of azole fungicides in fish samples. Alpha-(2,4-Dichlorophenyl)-1H-imidazole-1-ethanol (DCE) was used as the fragment dummy template for
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Nature communications, 11(1), 6242-6242 (2020-12-09)
DNA-templated synthesis takes advantage of the programmability of DNA-DNA interactions to accelerate chemical reactions under diluted conditions upon sequence-specific hybridization. While this strategy has proven advantageous for a variety of applications, including sensing and drug discovery, it has been so

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