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Merck
모든 사진(1)

Key Documents

140295

Sigma-Aldrich

Decanoyl chloride

98%

동의어(들):

Capric acid chloride

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About This Item

Linear Formula:
CH3(CH2)8COCl
CAS Number:
Molecular Weight:
190.71
Beilstein:
507055
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

6.57 (vs air)

Quality Level

분석

98%

형태

liquid

refractive index

n20/D 1.441 (lit.)

bp

94-96 °C/5 mmHg (lit.)

density

0.919 g/mL at 25 °C (lit.)

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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일반 설명

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

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

애플리케이션

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

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

284.0 °F

Flash Point (°C)

140 °C

개인 보호 장비

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


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문서 라이브러리 방문

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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