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30608

Supelco

1-Decanol

Selectophore™, ≥98.0%

Synonym(s):

n-Decyl alcohol, Alcohol C10

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About This Item

Linear Formula:
CH3(CH2)9OH
CAS Number:
112-30-1
Molecular Weight:
158.28
Beilstein:
1735221
EC Number:
203-956-9
MDL number:
MFCD00004747
UNSPSC Code:
26111700
PubChem Substance ID:
329753545
NACRES:
NA.05
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grade

for ion-selective electrodes

Quality Level

200

vapor density

4.5 (vs air)

vapor pressure

1 mmHg ( 70 °C)
8.25 mmHg ( 100 °C)

product line

Selectophore™

Assay

≥98.0% (GC)
≥98.0%

autoignition temp.

550 °F

refractive index

n20/D 1.437 (lit.)

bp

231 °C (lit.)

mp

5-7 °C (lit.)

solubility

H2O: slightly soluble 0.0211 g/L at 20 °C

density

0.829 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCO

InChI

1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3

InChI key

MWKFXSUHUHTGQN-UHFFFAOYSA-N

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General description

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Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

203.0 °F - Pensky-Martens closed cup

Flash Point(C)

95 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW4868

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Agnieszka Szarecka et al.
Biophysical journal, 93(6), 1895-1905 (2007-05-22)
The new crystal structures of the product-bound firefly luciferase combined with the previously determined substrate-free structures allow for a detailed analysis of the dynamics basis for the luciferase enzymatic activities. Using the Gaussian network model and the anisotropic network model
Maria Paola Tampieri et al.
Mycopathologia, 159(3), 339-345 (2005-05-11)
Many volatile oils are known to possess antifungal properties and are potentially applicable as antimycotic agents. By studying the efficacy of essential oils against different pathogenic mycetes, we have evaluated the in-vitro inhibiting activity of some essential oils and their
Maen M Husein et al.
Journal of colloid and interface science, 288(2), 457-467 (2005-06-02)
A novel method of preparing AgCl nanoparticles by mixing AgCl powder and a microemulsion consisting of dioctyldimethylammonium chloride/n-decanol/water/isooctane is introduced. This new method was discovered during the preparation of AgCl nanoparticles in single microemulsions by direct reaction with the dioctyldimethylammonium
M Doi et al.
The journal of peptide research : official journal of the American Peptide Society, 66(4), 181-189 (2005-09-06)
Bolaform amides were designed from N,N'-bis(carboethoxy-L-valinyl)-diaminoethane (1) by linking t-butyloxycarbonyl-valine through ethylenediamine (EDA) to enable spectroscopic and X-ray diffraction analyses. N,N'-Bis(Boc-L-valinyl)-diaminoethane (2) and N,N'-bis(Boc-D-valinyl)-diaminoethane (3) were composed of L-Val and D-Val, respectively. N-(Boc-L-valinyl)-N'-(Boc-D-valinyl)-diaminoethane (4) was composed of both L-Val and
Grit Neumann et al.
Applied and environmental microbiology, 72(6), 4232-4238 (2006-06-06)
The solvent-tolerant strain Pseudomonas putida DOT-T1E was grown in batch fermentations in a 5-liter bioreactor in the presence and absence of 10% (vol/vol) of the organic solvent 1-decanol. The growth behavior and cellular energetics, such as the cellular ATP content
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