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Merck

442539

Supelco

1-癸醇

analytical standard

别名:

C10 醇, 正癸醇

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About This Item

线性分子式:
CH3(CH2)9OH
CAS号:
分子量:
158.28
Beilstein:
1735221
EC號碼:
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:

等級

analytical standard

品質等級

蒸汽密度

4.5 (vs air)

蒸汽壓力

1 mmHg ( 70 °C)
8.25 mmHg ( 100 °C)

CofA

current certificate can be downloaded

自燃溫度

550 °F

包裝

ampule of 1000 mg

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.437 (lit.)

bp

231 °C (lit.)

mp

5-7 °C (lit.)

溶解度

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

密度

0.829 g/mL at 25 °C (lit.)

應用

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

形式

neat

儲存溫度

2-30°C

SMILES 字串

CCCCCCCCCCO

InChI

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

InChI 密鑰

MWKFXSUHUHTGQN-UHFFFAOYSA-N

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一般說明

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

應用

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.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Aquatic Chronic 3 - Eye Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

203.0 °F - Pensky-Martens closed cup

閃點(°C)

95 °C - Pensky-Martens closed cup

個人防護裝備

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


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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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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