추천 제품
Quality Level
제품 라인
ReagentPlus®
분석
99%
refractive index
n20/D 1.4804 (lit.)
bp
199-202 °C (lit.)
density
0.973 g/mL at 25 °C (lit.)
작용기
hydroxyl
SMILES string
OCCN1CCCCC1
InChI
1S/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2
InChI key
KZTWONRVIPPDKH-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
1-(2-Hydroxyethyl)piperidine (1-Piperidineethanol) has been used as the base quencher to determine the efficiency of the decomposition of photoacid generators.
Counter-ion used for investigations of skin permeation of flurbiprofen
Catalyst used for enantioselective synthesis
Amine quencher used during synthesis of photoacid generators for ArF lithography
Adsorbent for capture and release of pressurized carbon dioxide for greenhouse gas control
Catalyst used for enantioselective synthesis
Amine quencher used during synthesis of photoacid generators for ArF lithography
Adsorbent for capture and release of pressurized carbon dioxide for greenhouse gas control
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
156.2 °F - closed cup
Flash Point (°C)
69 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
J. Photopolym. Sci. Technol., 18, 407-414 (2005)
Journal of pharmaceutical sciences, 99(4), 1826-1837 (2009-11-07)
The aim of this work was to investigate the percutaneous absorption of flurbiprofen (FP) using counter-ions as enhancers as well as to compare their enhancing activity with penetration enhancers in vitro. The in vitro permeation studies of FP were performed
A standard addition technique to quantify photoacid generation in chemically amplified photoresist.
Chemistry of Materials, 13(11), 4154-4162 (2001)
Journal of the American Chemical Society, 127(35), 12206-12207 (2005-09-01)
An asymmetric autocatalytic reaction has been catalyzed by a mixture of chiral and achiral beta-amino alcohols. The absolute configuration of the highly enantioenriched obtained product (>98% ee) was shown to depend not only on the absolute configuration of the chiral
Chemistry Letters (Jpn), 37, 516-517 (2008)
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