Saltar al contenido
Merck

538639

Sigma-Aldrich

N,N-Dimethyldecylamine

≥90%

Sinónimos:

1-(Dimethylamino)decane

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
CH3(CH2)9N(CH3)2
Número de CAS:
Peso molecular:
185.35
Beilstein/REAXYS Number:
1738198
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥90%

refractive index

n20/D 1.431 (lit.)

bp

234 °C (lit.)

density

0.778 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCN(C)C

InChI

1S/C12H27N/c1-4-5-6-7-8-9-10-11-12-13(2)3/h4-12H2,1-3H3

InChI key

YWWNNLPSZSEZNZ-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Categorías relacionadas

General description

N,N-Dimethyldecylamine is a tertiary amine. It can be prepared by reacting N,N-dimethyldodecylamine, t-butyl hydroperoxide, vanadium oxyacetylacetonate and t-butyl alcohol.

Application

N,N-Dimethyldecylamine may be used as one of the reaction components in the preparation of:
  • comb-shaped quaternized poly(2,6-dimethylphenylene oxide) (PPO)
  • pore-expanded MCM-41 silica
  • QA C10 stationary phase bearing quaternary ammonium embedded between a propyl and a decyl chain

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

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


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Applications of pore-expanded MCM-41 silica: 4. Synthesis of a highly active base catalyst.
Das DD, et al.
Catalysis Communications, 8(5), 829-833 (2007)
Hydroperoxide oxidations catalyzed by metals. II. Oxidation of tertiary amines to amine oxides.
Sheng MN and Zajacek JG.
The Journal of Organic Chemistry, 33(2), 588-590 (1968)
Qiaoxia Liu et al.
Journal of separation science, 35(20), 2685-2692 (2012-09-26)
A stationary phase (named QA C10) with quaternary ammonium embedded between a propyl and a decyl chain was synthesized by immobilization of N,N-dimethyldecylamine on chloropropyl-silica surface. A set of representative neutral, basic, and acidic compounds was employed to evaluate its
Nanwen Li et al.
Journal of the American Chemical Society, 135(27), 10124-10133 (2013-06-01)
To produce an anion-conductive and durable polymer electrolyte for alkaline fuel cell applications, a series of quaternized poly(2,6-dimethyl phenylene oxide)s containing long alkyl side chains pendant to the nitrogen-centered cation were synthesized using a Menshutkin reaction to form comb-shaped structures.
Daria Szymaniak et al.
ChemPlusChem, 85(10), 2281-2289 (2020-09-23)
The synthesis and characteristics are presented of novel double-salt herbicidal ionic liquids (DSHILs) that contain 4-chloro-2-methylphenoxyacetate and trans-cinnamate anions. In the designed synthesis, an anion of natural origin and a herbicidal anion were combined with an amphiphilic bisammonium cation to

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico