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185205

Sigma-Aldrich

Myristoyl chloride

97%

Sinónimos:

Tetradecanoyl chloride

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About This Item

Fórmula lineal:
CH3(CH2)12COCl
Número de CAS:
112-64-1
Peso molecular:
246.82
Beilstein/REAXYS Number:
636924
EC Number:
203-994-6
MDL number:
MFCD00000741
UNSPSC Code:
12352100
PubChem Substance ID:
24850676
NACRES:
NA.22

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.449 (lit.)

bp

250 °C/100 mmHg (lit.)

mp

−1 °C (lit.)

density

0.908 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCC(Cl)=O

InChI

1S/C14H27ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3

InChI key

LPWCRLGKYWVLHQ-UHFFFAOYSA-N

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Application

Myristoyl chloride was used in the synthesis of 6-azafulleroid-6-deoxy-2,3-di-O-myristoylcellulose. It was used in N-acylation of chitosan to introduce hydrophobicity for use as matrix for drug delivery. It was used in the synthesis of semi-crystalline dendritic poly(ether-amide) derivatives.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H290,H314

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Stearoyl chloride technical, ≥90% (GC), strongly brown

Sigma-Aldrich

85730

Stearoyl chloride

Dodecanoyl chloride purum, ≥97.5% (GC)

Sigma-Aldrich

61670

Dodecanoyl chloride

Undecanoyl chloride 99%

Sigma-Aldrich

249432

Undecanoyl chloride

Octanoyl chloride 99%

Sigma-Aldrich

O4733

Octanoyl chloride

Canh Le Tien et al.
Journal of controlled release : official journal of the Controlled Release Society, 93(1), 1-13 (2003-11-07)
N-acylation of chitosan with various fatty acid (C(6)-C(16)) chlorides increased its hydrophobic character and made important changes in its structural features. Unmodified chitosan exhibited a low degree of order (DO) and a weak tablet crushing strength. Chitosan acylated with a
Synthesis and crystallinity of dendritic poly (ether-amide) derivatives.
Wei H, et al.
Eur. Polymer J., 38(9), 1899-1905 (2002)
Diego Romano Perinelli et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 109, 93-102 (2016-10-04)
Toxicity is one of the main concerns limiting the use of surfactants. Many efforts have been devoted to the development of new amphiphilic molecules characterized by a lower toxicological profile and environmental impact. N-acyl amino acids are a class of
Nobuhiko Ichihara et al.
Carbohydrate research, 346(15), 2515-2518 (2011-09-17)
6-Azafulleroid-6-deoxy-2,3-di-O-myristoylcellulose (3) was synthesized from 6-azido-6-deoxycellulose (1) by two reaction steps. The myristoylation of compound 1 with myristoyl chloride/pyridine proceeded smoothly to give 6-azido-6-deoxy-2,3-di-O-myristoylcellulose (2) in 97.0% yield. The reaction of compound 2 with fullerene (C(60)) was carried out by
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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