185205
肉豆蔻酰氯
97%
别名:
十四酰氯
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线性分子式:
CH3(CH2)12COCl
化学文摘社编号:
分子量:
246.82
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-994-6
Beilstein/REAXYS Number:
636924
MDL number:
产品名称
肉豆蔻酰氯, 97%
InChI key
LPWCRLGKYWVLHQ-UHFFFAOYSA-N
InChI
1S/C14H27ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3
SMILES string
CCCCCCCCCCCCCC(Cl)=O
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.)
functional group
acyl chloride
Quality Level
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Application
肉豆蔻酰氯已被用于合成6-氮杂富勒基-6-脱氧-2,3-二-O-肉豆蔻酰纤维素。它已被用于壳聚糖的N-酰化来引入疏水性以用作药物递送的基质。它已被用于合成半结晶树状聚（醚-酰胺）衍生物。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
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
法规信息
危险化学品
此项目有
Synthesis and crystallinity of dendritic poly (ether-amide) derivatives.
Wei H, et al.
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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
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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