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Merck
모든 사진(1)

주요 문서

85730

Sigma-Aldrich

Stearoyl chloride

technical, ≥90% (GC), strongly brown

동의어(들):

Octadecanoyl chloride

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About This Item

Linear Formula:
CH3(CH2)16COCl
CAS Number:
Molecular Weight:
302.92
Beilstein:
639784
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Quality Level

분석

≥90% (GC)

양식

liquid

색상

strongly brown

refractive index

n20/D 1.454 (lit.)

bp

174-178 °C/2 mmHg (lit.)

mp

21-22 °C (lit.)

density

0.897 g/mL at 25 °C (lit.)

작용기

acyl chloride

SMILES string

CCCCCCCCCCCCCCCCCC(Cl)=O

InChI

1S/C18H35ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3

InChI key

WTBAHSZERDXKKZ-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Stearoyl chloride can modify cellulose diacetate (CDA) by replacing residual free hydroxyl groups in synthesizing materials that are used to produce surgical masks, smocks and other industrial products to absorb dust and haze-fog. It can be used in the synthesis of ultrastable coaxial cable-like superhydrophobic mesh. It is also used in the synthesis of stearoyl modified chitosan as drug vehicles for paclitaxel delivery.

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Skin Corr. 1B

보충제 위험성

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point (°F)

329.0 °F - closed cup

Flash Point (°C)

165 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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문서 라이브러리 방문

Ultrastable coaxial cable-like superhydrophobic mesh with self-adaption effect: facile synthesis and oil/water separation application.
Xiao C, et al.
Journal of Material Chemistry A, 4(21), 8080-8090 (2016)
Amphiphilic nanoparticles based on poly (vinyl pyrrolidone) and stearoyl modified chitosan as drug vehicles for paclitaxel delivery.
Liu Z, et al.
Materials Letters, 185, 226-229 (2016)
Çağla Koşak Söz et al.
ACS applied materials & interfaces, 10(43), 37478-37488 (2018-10-27)
We introduce the design of Janus-type paper sheets where one side of the paper exhibits superhydrophobic properties, whereas the other side of the sheet remains hydrophilic and therefore can take up aqueous solutions by capillary wicking. Such papers are being
Acylation of Cellulose Diacetate by Stearoyl Chloride and Characterization for the Acylated Product.
Wang Q, et al.
J. Polym. Mater., 32(4) (2015)
Shuangfei Wang et al.
Carbohydrate polymers, 195, 39-44 (2018-05-29)
Superhydrophobic surfaces have attracted great attention due to their attractive properties. Biopolymer-based low-cost and environmentally-friendly superhydrophobic coatings with easy-to-perform fabrication methods are always desirable. Herein, we report superhydrophobic surfaces using a one-step spray-coating of chitosan-based nanoparticles. The particles were easily

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