44095
1-Dodecanol
Selectophore™, ≥98.0%
동의어(들):
Alcohol C12, Dodecyl alcohol, Lauryl alcohol
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모든 사진(1)
About This Item
Linear Formula:
CH3(CH2)11OH
CAS Number:
Molecular Weight:
186.33
Beilstein:
1738860
EC Number:
MDL number:
UNSPSC 코드:
26111700
eCl@ss:
39020229
PubChem Substance ID:
NACRES:
NA.05
bp:
260-262 °C (lit.)
vapor pressure:
0.1 mmHg ( 20 °C)
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추천 제품
vapor density
7.4 (vs air)
Quality Level
vapor pressure
0.1 mmHg ( 20 °C)
설명
for ion-selective electrodes
제품 라인
Selectophore™
분석
≥98.0% (GC)
≥98.0%
autoignition temp.
500 °F
expl. lim.
4 %
refractive index
n20/D 1.442 (lit.)
bp
260-262 °C (lit.)
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일반 설명
1-Dodecanol is an n-alkano organic compound.[1]
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애플리케이션
It is may be used to investigate the thermal properties of caprylic acid using differential scanning calorimetry.[1] It may also be used as extraction solvent during determination of five kinds of polycyclic aromatic hydrocarbons in water samples, using dispersive liquid-liquid microextraction based on solidification of floating organic droplet method (DLLME-SFO).[2]
법적 정보
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
249.8 °F - closed cup
Flash Point (°C)
121 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
이미 열람한 고객
Thermal performance of caprylic acid/1-dodecanol eutectic mixture as phase change material (PCM).
Zuo, Jianguo, Weizhong Li, and Lindong Weng
Energy and Buildings, 43.1, 207-210 (2011)
Hui Xu et al.
Analytica chimica acta, 636(1), 28-33 (2009-02-24)
A new dispersive liquid-liquid microextraction based on solidification of floating organic droplet method (DLLME-SFO) was developed for the determination of five kinds of polycyclic aromatic hydrocarbons (PAHs) in environmental water samples. In this method, no specific holder, such as the
Samuel D Banister et al.
Bioorganic & medicinal chemistry letters, 21(12), 3622-3626 (2011-05-11)
A series of N-substituted 4-azahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)]dodecan-3-ols incorporating the respective arylalkyl subunits from several known sigma (σ) receptor ligands were synthesized and evaluated for their affinity against σ receptors and dopamine receptors. The hybrid trishomocubane-derived ligands (4-6) showed good selectivity for σ(1)
Kun Liu et al.
Journal of chromatography. A, 1227, 96-104 (2012-01-24)
Seven crosslinking monomers, i.e., 1,3-butanediol dimethacrylate (1,3-BDDMA), 1,4-butanediol dimethacrylate (1,4-BDDMA), neopentyl glycol dimethacrylate (NPGDMA), 1,5-pentanediol dimethacrylate (1,5-PDDMA), 1,6-hexanediol dimethacrylate (1,6-HDDMA), 1,10-decanediol dimethacrylate (1,10-DDDMA), and 1,12-dodecanediol dimethacrylate (1,12-DoDDMA), were used to synthesize highly cross-linked monolithic capillary columns for reversed-phase liquid chromatography
Chris Grant et al.
Biotechnology and bioengineering, 109(9), 2179-2189 (2012-04-05)
This article describes the first reported microwell whole-cell bioconversion using a water immiscible substrate that matches the specific activity and yield achieved in a 1.2 L stirred tank bioreactor. Maximum yields of 0.6 g/L(total) 1-dodecanol achieved in 24 h compare
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