Decylamine

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Structural formula
Structural formula of decylamine
General
Surname Decylamine
other names

1-aminodecane

Molecular formula C 10 H 23 N
Brief description

colorless liquid

External identifiers / databases
CAS number
EC number 217-957-7
ECHA InfoCard 100.016.326
PubChem 8916
Wikidata Q5493262
properties
Molar mass 157.30 g mol −1
Physical state

liquid

density

0.79 g cm −3

Melting point

17 ° C

boiling point

220.5 ° C

Vapor pressure

0.896 mbar (50 ° C)

solubility
  • very heavy in water (0.55 g l −1 at 25 ° C)
  • miscible with ethanol
Refractive index

1.436 (20 ° C)

safety instructions
GHS labeling of hazardous substances
06 - Toxic or very toxic 05 - Corrosive 09 - Dangerous for the environment

danger

H and P phrases H: 301-311-314-400
P: 273-280-301 + 310-305 + 351 + 338-310
Toxicological data
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Decylamine is a chemical compound from the group of alkylamines .

properties

Decylamine is a colorless liquid that is very difficult to ignite and is very sparingly soluble in water.

use

Decylamine can for the synthesis of dynamin inhibitors as Dynole® 2-24 as well as a coordinating solvent in the thermolysis of lead piperidine - and lead-tetrahydroquinoline dithiocarbamate complexes to lead sulfide - nanoparticles are used. Derivatives such as N, N-dimethyldecylamine oxide are used in cosmetics.

Individual evidence

  1. ↑ a b c d e f g h i j k l Entry on decylamine in the GESTIS substance database of the IFA , accessed on January 9, 2019(JavaScript required) .
  2. ↑ William M. Haynes: CRC Handbook of Chemistry and Physics, 94th Edition: . CRC Press, 2013, ISBN 978-1-4665-7115-0 , pp. 143 ( limited preview in Google Book search).
  3. ↑ a b Data sheet Decylamine, ≥99.0% (GC) from Sigma-Aldrich , accessed on May 5, 2015 ( PDF ).
  4. ↑ https://pubs.rsc.org/en/content/articlelanding/2012/dt/c2dt30282a/unauth#!divAbstract Thermolysis of lead complexes to PbS
  5. ^ GWA Milne: Gardner's Commercially Important Chemicals: Definitions, Trade Names, and Properties . John Wiley & Sons, 2005, ISBN 0-471-73661-9 , pp. 180 ( limited preview in Google Book Search).