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156930

Sigma-Aldrich

Lauroyl chloride

98%

Sinônimo(s):

Dodecanoyl chloride

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About This Item

Fórmula linear:
CH3(CH2)10COCl
Número CAS:
112-16-3
Peso molecular:
218.76
Beilstein:
1281201
Número CE:
203-941-7
Número MDL:
MFCD00000740
Código UNSPSC:
12352100
ID de substância PubChem:
24849648
NACRES:
NA.22

Ensaio

98%

forma

liquid

índice de refração

n20/D 1.445 (lit.)

pb

134-137 °C/11 mmHg (lit.)

solubilidade

methanol: soluble 100 mg/mL, clear

densidade

0.946 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCCCCC(Cl)=O

InChI

1S/C12H23ClO/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3

chave InChI

NQGIJDNPUZEBRU-UHFFFAOYSA-N

Categorias relacionadas

Aplicação

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

Pictogramas

Corrosion
GHS05

Palavra indicadora

Danger

Frases de perigo

H314

Classificações de perigo

Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

284.0 °F - closed cup

Ponto de fulgor (°C)

140 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

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Feng Peng et al.
Carbohydrate research, 343(17), 2956-2962 (2008-09-17)
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
Conghu Li et al.
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
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
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
Parvaiz Ahmad Bhat et al.
Food chemistry, 340, 128168-128168 (2020-10-05)
The chemical instability of Citral in acidic conditions is viewed as hurdle to commercialize it in food/beverage industries. We attempted to stabilize citral in various single and mixed surfactant systems at pH 1.0 and temperature 25 °C. The study highlights the
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