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18-0320

1-Dodecanol

Name: 1-Dodecanol
Brand: SAJ

SAJ special grade, ≥97.0%

Sinônimo(s):

Alcohol C₁₂, Dodecyl alcohol, Lauryl alcohol

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About This Item

Fórmula linear:

CH₃(CH₂)₁₁OH

Número CAS:

112-53-8

Peso molecular:

186.33

Beilstein:

1738860

Número CE:

203-982-0

Número MDL:

MFCD00004753

Código UNSPSC:

12352104

ID de substância PubChem:

329751611

grau

SAJ special grade

densidade de vapor

7.4 (vs air)

pressão de vapor

0.1 mmHg ( 20 °C)

Ensaio

≥97.0%

forma

solid

temperatura de autoignição

500 °F

Lim. expl.

4 %

disponibilidade

available only in Japan

índice de refração

n20/D 1.442 (lit.)

pb

260-262 °C (lit.)

pf

22-26 °C (lit.)

densidade

0.833 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCCCCCO

InChI

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

chave InChI

LQZZUXJYWNFBMV-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Pictogramas

GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H319,H410

Declarações de precaução

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

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

249.8 °F - closed cup

Ponto de fulgor (°C)

121 °C - closed cup

Equipamento de proteção individual

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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