ChemicalBook > CAS DataBase List > Tetrabutylammonium azide

Tetrabutylammonium azide

Product Name
Tetrabutylammonium azide
CAS No.
993-22-6
Chemical Name
Tetrabutylammonium azide
Synonyms
TETRA-N-BUTYLAMMONIUM AZIDE;tetrabutylammoniun azide;Tetrabutylammonium a;TETRABUTYLAMMONIUM AZIDE;Tetrabutylammonium nitride;n,n,n-tributyl-1-butanaminiuazide;Tetra-n-butylammonium azide, 90+%;N,N,N-Tributyl-1-butanaminium azide;1-Butanaminium, N,N,N-tributyl-, azide;1-Butanaminium, N,N,N-tributyl-, azide (1:1)
CBNumber
CB0463838
Molecular Formula
C16H36N4
Formula Weight
284.48
MOL File
993-22-6.mol
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Tetrabutylammonium azide Property

Melting point:
84-88 °C (lit.)
storage temp. 
2-8°C
Water Solubility 
Soluble in water
form 
powder to crystal
color 
White to Light yellow
Sensitive 
Hygroscopic
CAS DataBase Reference
993-22-6
EPA Substance Registry System
1-Butanaminium, N,N,N-tributyl-, azide (993-22-6)
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Safety

Hazard Codes 
T,N
Risk Statements 
11-50/53-36/37/38-32-25
Safety Statements 
15-36/37/39-45-61-60-26
RIDADR 
1325
WGK Germany 
3
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29239000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P273Avoid release to the environment.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
651664
Product name
Tetrabutylammonium azide
Packaging
5g
Price
$67.8
Updated
2024/03/01
Sigma-Aldrich
Product number
651664
Product name
Tetrabutylammonium azide
Packaging
25g
Price
$215
Updated
2024/03/01
TCI Chemical
Product number
T0920
Product name
Tetrabutylammonium Azide
Purity
>95.0%(T)
Packaging
5g
Price
$95
Updated
2024/03/01
TCI Chemical
Product number
T0920
Product name
Tetrabutylammonium Azide
Purity
>95.0%(T)
Packaging
25g
Price
$336
Updated
2024/03/01
Usbiological
Product number
291040
Product name
Tetrabutylammonium azide
Packaging
5g
Price
$460
Updated
2021/12/16
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Tetrabutylammonium azide Chemical Properties,Usage,Production

Uses

Tetrabutylammonium azide can be used as a reagent for the synthesis of:

  • Heteroarylannulated bicyclic morpholines
  • Cyanimide-based inhibitors of cathepsin C
  • Trimethylene carbonate
  • Aerobic oxidative transformation of primary azides to nitriles
  • Substitution reactions at tetracoordinate boron


It is also used as a catalyst for cyclic carbonate formation.

Tetrabutylammonium azide Preparation Products And Raw materials

Raw materials

Preparation Products

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Tetrabutylammonium azide Suppliers

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View Lastest Price from Tetrabutylammonium azide manufacturers

Career Henan Chemical Co
Product
N,N,N-Tributyl-1-butanaminium azide 993-22-6
Price
US $1.00/g
Min. Order
1g
Purity
Min98%HPLC
Supply Ability
g/kg/ton
Release date
2020-01-09

993-22-6, Tetrabutylammonium azideRelated Search:


  • TETRA-N-BUTYLAMMONIUM AZIDE
  • TETRABUTYLAMMONIUM AZIDE
  • n,n,n-tributyl-1-butanaminiuazide
  • N,N,N-Tributyl-1-butanaminium azide
  • Tetra-n-butylammonium azide, 90+%
  • Tetrabutylammonium nitride
  • 1-Butanaminium, N,N,N-tributyl-, azide
  • 1-Butanaminium, N,N,N-tributyl-, azide (1:1)
  • Tetrabutylammonium a
  • tetrabutylammoniun azide
  • 993-22-6
  • CH3CH2CH2CH24NN3
  • C16H36N4
  • C16H36NN3
  • Quaternary Ammonium Compounds
  • Ammonium Polyhalides, etc. (Quaternary)
  • C-X Bond Formation (Non-Halogen)
  • Synthetic Reagents
  • Azidation/Diazo Transfer
  • Ammonium Polyhalides, etc. (Quaternary)
  • Quaternary Ammonium Compounds
  • Azidation/Diazo TransferChemical Ligation
  • Azide Sources
  • Click Chemistry
  • C-X Bond Formation (Non-Halogen)
  • Synthetic Reagents