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538639

Sigma-Aldrich

N,N-Dimethyldecylamine

≥90%

Synonym(s):

1-(Dimethylamino)decane

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About This Item

Linear Formula:
CH3(CH2)9N(CH3)2
CAS Number:
1120-24-7
Molecular Weight:
185.35
Beilstein:
1738198
EC Number:
214-302-7
MDL number:
MFCD00015060
UNSPSC Code:
12352100
PubChem Substance ID:
24878348
NACRES:
NA.22

Quality Level

100

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

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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
GHS07

Signal Word

Warning

Hazard Statements

H302 - H315

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

197.6 °F - closed cup

Flash Point(C)

92 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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.
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
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

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