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About This Item
Linear Formula:
CH3(CH2)10COCl
CAS Number:
Molecular Weight:
218.76
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-941-7
Beilstein/REAXYS Number:
1281201
MDL number:
grade
purum
Quality Level
assay
≥97.5% (GC)
refractive index
n20/D 1.445
mp
-13--10 °C
density
0.922 g/mL at 20 °C
functional group
acyl chloride
SMILES string
CCCCCCCCCCCC(Cl)=O
InChI
1S/C12H23ClO/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3
InChI key
NQGIJDNPUZEBRU-UHFFFAOYSA-N
Application
Dodecanoyl chloride aslo known as lauroyl chloride is an acid chloride that can be used as a reagent for the surface modification of:
It can also be used as a:
- Chitosans, by converting it into acylated chitosans for increasing solubility in organic solvents.
- Microfibrillated cellulose (MFC) for improving dispersibility in biopolyamide nanocomposites.
It can also be used as a:
- Starting material for the synthesis of (R)-3-aminotetradecanoic acid (iturinic acid).
- Reagent for the preparation of (3,6-bis(dodecanamido)-2,7-dibromo-9-dodecyl-9H-carbazole).This amide intermediate can be further used in the synthesis of azomethine-bridged ladder-type poly( p-phenylene)s.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
284.0 °F - closed cup
flash_point_c
140 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Characterization of chemical and solid state structures of acylated chitosans
Zong Z, et al.
Polymer, 41(3), 899-906 (2000)
Synthesis of fully soluble azomethine-bridged ladder-type poly (p-phenylenes) by Bischler- Napieralski reaction
Chen Y, et al.
Macromolecules, 43(24), 10216-10220 (2010)
Novel stereoselective synthesis of (R)-3-aminotetradecanoic acid (Iturinic acid)
Temperini A, et al.
Letters in Organic Chemistry, 6(1), 22-24 (2009)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 61670-250ML | 04061832700359 |
| 61670-1L | 04061836692964 |
