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CdO/CdA

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18-0320

1-Dodecanol

Name: 1-Dodecanol
Brand: SAJ

SAJ special grade, ≥97.0%

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:

12352104

ID PubChem:

329751611

Grado

SAJ special grade

Densità del vapore

7.4 (vs air)

Tensione di vapore

0.1 mmHg ( 20 °C)

Saggio

≥97.0%

Forma fisica

solid

Temp. autoaccensione

500 °F

Limite di esplosione

4 %

Disponibilità

available only in Japan

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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Pittogrammi

GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H319,H410

Consigli di prudenza

P264 - P273 - P280 - P305 + P351 + P338 - P337 + P313 - P391

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, type P3 (EN 143) respirator cartridges

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Highly crosslinked polymeric monoliths for reversed-phase capillary liquid chromatography of small molecules.

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

Molecular hybridization of 4-azahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)]dodecane-3-ol with sigma (σ) receptor ligands modulates off-target activity and subtype selectivity.

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)

Tools for characterizing the whole-cell bio-oxidation of alkanes at microscale.

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

2,5,6,9,10-Pentabromocyclododecanols (PBCDOHs): a new class of HBCD transformation products.

Norbert V Heeb et al.

Chemosphere, 88(5), 655-662 (2012-04-24)

Pentabromocyclododecanols (PBCDOHs) are potential environmental transformation products of hexabromocyclododecanes (HBCDs). They are also potential stage one metabolites of biological HBCD transformations. Herein, we present analytical evidence that PBCDOHs are also constituents of technical HBCDs and flame-proofed polystyrenes (FP-PSs). PBCDOHs are

Membrane-assisted extractive butanol fermentation by Clostridium saccharoperbutylacetonicum N1-4 with 1-dodecanol as the extractant.

Shigemitsu Tanaka et al.

Bioresource technology, 116, 448-452 (2012-05-12)

A polytetrafluoroethylene (PTFE) membrane was used in membrane-assisted extractive (MAE) fermentation of acetone-butanol-ethanol (ABE) by Clostridium saccharoperbutylacetonicum N1-4. The growth inhibition effects of 1-dodecanol, which has a high partition coefficient for butanol, can be prevented by employing 1-dodecanol as an

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