156930
Lauroyl chloride
98%
Synonym(s):
Dodecanoyl chloride
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About This Item
Linear Formula:
CH3(CH2)10COCl
CAS Number:
Molecular Weight:
218.76
Beilstein:
1281201
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
liquid
refractive index
n20/D 1.445 (lit.)
bp
134-137 °C/11 mmHg (lit.)
solubility
methanol: soluble 100 mg/mL, clear
density
0.946 g/mL at 25 °C (lit.)
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
Lauroyl chloride was used:
- as tailoring agent for chemical modification of nanocelluloses of different length, nanofibrillated cellulose and cellulose nanocrystals
- in the preparation of acylated collagen with water solubility and better surface activity
- as organic low-friction boundary lubricant in the preparation of novel polyvinyl alcohol hydrogel
- in the synthesis of hemicellulose-based hydrophobic biomaterials
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
284.0 °F - closed cup
Flash Point(C)
140 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Ana G Cunha et al.
Langmuir : the ACS journal of surfaces and colloids, 30(31), 9327-9335 (2014-07-22)
Nanocelluloses are bio-based nanoparticles of interest as stabilizers for oil-in-water (o/w) Pickering emulsions. In this work, the surface chemistry of nanocelluloses of different length, nanofibrillated cellulose (NFC, long) and cellulose nanocrystals (CNC, short), was successfully tailored by chemical modification with
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Hemicellulose-based hydrophobic biomaterials with degrees of substitution ranging from 0.46 to 1.54 were synthesized under mild conditions in homogeneous media (N,N-dimethylformamide-lithium chloride) by reacting the native wheat straw hemicellulosic polymers with lauroyl chloride using 4-dimethylaminopyridine as a catalyst. Other catalysts
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Michelle M Blum et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 100(7), 1755-1763 (2012-07-19)
A novel material design was developed by functionalizing polyvinyl alcohol hydrogel with an organic low-friction boundary lubricant (molar ratios of 0.2, 0.5, and 1.0 moles of lauroyl chloride). The hydrogels were fabricated using two different techniques. First, the boundary lubricant
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International journal of biological macromolecules, 57, 92-98 (2013-03-19)
A new kind of acylated collagen with water solubility and better surface activity was prepared via reaction of pepsin-solubilized calf skin collagen with lauroyl chloride and succinic anhydride in this paper. The equilibrium surface tension and the isoelectric point were
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