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44095

Supelco

1-Dodecanol

Selectophore™, ≥98.0%

Sinonimo/i:

Alcohol C12, Dodecyl alcohol, Lauryl alcohol

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About This Item

Formula condensata:
CH3(CH2)11OH
Numero CAS:
112-53-8
Peso molecolare:
186.33
Beilstein:
1738860
Numero CE:
203-982-0
Numero MDL:
MFCD00004753
Codice UNSPSC:
26111700
eCl@ss:
39020229
ID PubChem:
329756451
NACRES:
NA.05

Grado

for ion-selective electrodes

Livello qualitativo

200

Densità del vapore

7.4 (vs air)

Tensione di vapore

0.1 mmHg ( 20 °C)

Nome Commerciale

Selectophore™

Saggio

≥98.0% (GC)
≥98.0%

Temp. autoaccensione

500 °F

Limite di esplosione

4 %

Indice di rifrazione

n20/D 1.442 (lit.)

P. eboll.

260-262 °C (lit.)

Punto di fusione

22-26 °C (lit.)

Densità

0.833 g/mL at 25 °C (lit.)

Stringa SMILE

CCCCCCCCCCCCO

InChI

1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3
LQZZUXJYWNFBMV-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

1-Dodecanol is an n-alkano organic compound.
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Applicazioni

It is may be used to investigate the thermal properties of caprylic acid using differential scanning calorimetry. 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).

Note legali

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H319,H410

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

249.8 °F - closed cup

Punto d’infiammabilità (°C)

121 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCK7720
BCCF0024
BCCC1517
BCBW1615
BCBS1957V

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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
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
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)
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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