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140295

Sigma-Aldrich

Decanoyl chloride

98%

Synonym(s):

Capric acid chloride

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100 ML
$52.30
500 ML
$138.00

About This Item

Linear Formula:
CH3(CH2)8COCl
CAS Number:
112-13-0
Molecular Weight:
190.71
Beilstein/REAXYS Number:
507055
EC Number:
203-938-0
MDL number:
MFCD00000771
UNSPSC Code:
12352100
PubChem Substance ID:
24848464
NACRES:
NA.22

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vapor density

6.57 (vs air)

assay

98%

form

liquid

refractive index

n20/D 1.441 (lit.)

bp

94-96 °C/5 mmHg (lit.)

density

0.919 g/mL at 25 °C (lit.)

functional group

acyl chloride

SMILES string

CCCCCCCCCC(Cl)=O

InChI

1S/C10H19ClO/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3

InChI key

IPIVAXLHTVNRBS-UHFFFAOYSA-N

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General description

Decanoyl chloride enhances the activity of proleather from Bacillus sp. during the synthesis of poly(lactic acid) in organic solvents[1].

Decanoyl chloride is used as a reactive acylating agent in organic synthesis. It is also employed in the formation of amides and esters.[2]

Application

Decanoyl chloride was used in the synthesis of oligomers composed of alternating 2,6-diaminopyridine and 2,6-pyridinedicarbonyl units[3].

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

284.0 °F

flash_point_c

140 °C

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL3013
BCCF5744
BCCF1777
BCCD3741
BCBZ6860

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Multivariate CuBTC metal--organic framework with enhanced selectivity, stability, compatibility, and processability
Peterson GW, et al.
Chemistry of Materials, 31(20), 8459-8465 (2019)
V Berl et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 7(13), 2798-2809 (2001-08-07)
Molecular strands composed of alternating 2,6-diaminopyridine and 2,6-pyridinedicarbonyl units have been designed to self-organize into single stranded helical structures upon forming intramolecular hydrogen bonds. Pentameric strands 11, 12, and 14, heptameric strands 1 and 20, and undecameric strand 15 have
Kelley A Distel et al.
Bioresource technology, 96(5), 617-623 (2004-10-27)
Proleather from Bacillus sp. was chemically modified with decanoyl chloride for enhanced activity for the preparation of poly(lactic acid) in organic solvents. The modified enzyme was highly soluble (up to 44 mg-protein/ml) and active in various organic solvents including chloroform
Dalia S Abdelhamid et al.
Biomaterials, 53, 32-39 (2015-04-22)
Cardiovascular disease initiates with the atherogenic cascade of scavenger receptor- (SR-) mediated oxidized low-density lipoprotein (oxLDL) uptake. Resulting foam cell formation leads to lipid-rich lesions within arteries. We designed amphiphilic macromolecules (AMs) to inhibit these processes by competitively blocking oxLDL
Janclei P Coutinho et al.
Talanta, 134, 256-263 (2015-01-27)
In this work a multivariate statistical tool (Derringer and Suich optimization) was proposed for the separation of seventeen capsinoids (natural and synthetic) using the UHPLC-DAD chromatography. Capsinoids were analyzed at 280 nm. The variables optimized were the mobile phase (water

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