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442539

Supelco

1-Decanol

analytical standard

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/REAXYS Number:
1735221
EC Number:
203-956-9
MDL number:
MFCD00004747
UNSPSC Code:
12000000
PubChem Substance ID:
24867896

grade

analytical standard

Quality Level

100

vapor density

4.5 (vs air)

vapor pressure

1 mmHg ( 70 °C)
8.25 mmHg ( 100 °C)

CofA

current certificate can be downloaded

autoignition temp.

550 °F

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

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.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-30°C

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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Related Categories

General description

1-Decanol can be obtained via decomposition of decyl hydroperoxide or dehydrogenation of 1-decene, followed by hydrolysis.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

Application

1-Decanol can find applications as a solvent in order to recover morpholine, via extraction of morpholine from the aqueous effluent in rubber, petrochemical, dye, coking plants, resin and also organo-chemical industries.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

wgk_germany

WGK 1

flash_point_f

203.0 °F

flash_point_c

95 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LRAD4483
LRAD1573
LRAC9571
LRAC7358
LRAC5007

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Groundwater Chemicals Desk Reference (2010)
Isobaric phase equilibrium of morpholine+ 1-decanol, volumetric properties and molar refractivity from 293.15 to 333.15 K of morpholine+ 1-decanol and 1-octanol+ toluene system with applications of Prigogine?Flory?Patterson theory
Kumari A, et al.
Thermochimica Acta, 649, 41-53 (2017)
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
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
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
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