모든 사진(4)
About This Item
Linear Formula:
CH3(CH2)15OH
CAS Number:
Molecular Weight:
242.44
Beilstein:
1748475
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor density
8.34 (vs air)
Quality Level
vapor pressure
<0.01 mmHg ( 43 °C)
제품 라인
ReagentPlus®
분석
99%
형태
solid
autoignition temp.
483 °F
expl. lim.
8 %
bp
179-181 °C/10 mmHg (lit.)
mp
48-50 °C (lit.)
solubility
ethanol: soluble 100 mL/mL, clear to very slightly hazy, colorless
density
0.818 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCCCCCCCCO
InChI
1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3
InChI key
BXWNKGSJHAJOGX-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
1-Hexadecanol is a fatty alcohol used in surfactants, lubricants, detergents, pharmaceuticals and cosmetics.
애플리케이션
1-Hexadecanol has been used in preparation of:
- (±)-2-methoxyheptadecanoic acid (fatty acid)
- high-chain fatty acid esters of 1-hexadecanol, novel organic phase change material for thermal energy storage
- hexadecane (alkane) in the presence of membrane fraction of Vibrio furnissii M1
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
nwg
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Néstor M Carballeira et al.
Pure and applied chemistry. Chimie pure et appliquee, 84(9), 1867-1875 (2012-11-03)
The fatty acids (±)-2-methoxy-6Z-heptadecenoic acid (1), (±)-2-methoxy-6-heptadecynoic acid (2) and (±)-2-methoxyheptadecanoic acid (3) were synthesized and their inhibitory activity against the Leishmania DNA topoisomerase IB enzyme (LdTopIB) determined. Acids 1 and 2 were synthesized from 4-bromo-1-pentanol, the former in ten
High-chain fatty acid esters of 1-hexadecanol for low temperature thermal energy storage with phase change materials.
Aydin AA and Aydin A.
Solar Energy Mat. and Solar Cells, 96, 93-100 (2012)
S Karen Gomez et al.
BMC plant biology, 9, 10-10 (2009-01-24)
Most vascular flowering plants have the capacity to form symbiotic associations with arbuscular mycorrhizal (AM) fungi. The symbiosis develops in the roots where AM fungi colonize the root cortex and form arbuscules within the cortical cells. Arbuscules are enveloped in
Myong-Ok Park
Journal of bacteriology, 187(4), 1426-1429 (2005-02-03)
Alkane biosynthesis in the bacterium Vibrio furnissii M1 involves the synthesis of long-chain alkanes via 1-alcohol. Evidence for this novel pathway are the following. (i) Both even- and odd-carbon-number n-alkanes were produced from glucose, while only even-carbon-number fatty acids were
Toru Uyama et al.
The Journal of biological chemistry, 290(28), 17520-17534 (2015-05-29)
Phospholipase A/acyltransferase (PLA/AT)-3 (also known as H-rev107 or AdPLA) was originally isolated as a tumor suppressor and was later shown to have phospholipase A1/A2 activity. We have also found that the overexpression of PLA/AT-3 in mammalian cells results in specific
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