61670
Dodecanoyl chloride
purum, ≥97.5% (GC)
Synonym(s):
Lauroyl chloride
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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:
InChI key
NQGIJDNPUZEBRU-UHFFFAOYSA-N
InChI
1S/C12H23ClO/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3
SMILES string
CCCCCCCCCCCC(Cl)=O
grade
purum
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
Quality Level
Related Categories
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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Novel stereoselective synthesis of (R)-3-aminotetradecanoic acid (Iturinic acid)
Temperini A, et al.
Letters in Organic Chemistry, 6(1), 22-24 (2009)
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)
Characterization of chemical and solid state structures of acylated chitosans
Zong Z, et al.
Polymer, 41(3), 899-906 (2000)
The effect of surface modification of microfibrillated cellulose (MFC) by acid chlorides on the structural and thermomechanical properties of biopolyamide 4.10 nanocomposites
Leszczynska, A, et al.
Industrial Crops and Products, 116(3), 97-108 (2018)
Sanna Virtanen et al.
Carbohydrate polymers, 177, 105-115 (2017-10-01)
Using softwood pulp as the starting material, the synthesis of regioselectively substituted mixed cellulose esters with varying degree of substitution and ratio of short/long chains was successfully completed. The structures of the cellulose esters were characterised. The impact of the
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