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CAS RN: 93183-36-9 | Product Number: D6204

Diisopropylammonium Tetrazol-1-ide


Purity: >98.0%(T)(HPLC)
Synonyms:
  • Diisopropylammonium Tetrazolide
Product Documents:
5G
100,00 €
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25G
298,00 €
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Product Number D6204
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__6H__1__5N·CH__2N__4 = 171.25 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Air Sensitive,Hygroscopic,Heat Sensitive
Packaging and Container 5G-Glass Bottle with Plastic Insert (View image)
CAS RN 93183-36-9
Reaxys Registry Number 3569216
Specifications
Appearance White to Light yellow powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Melting point 150.0 to 154.0 °C
NMR confirm to structure
Properties (reference)
Melting Point 152 °C
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
Related Laws:
Transport Information:
HS Number 2933998090
Application
TCI Practical Example: Phosphoroamidite Synthesis Using Diisopropylammonium Tetrazole

 TCI Practical Example: Phosphoroamidite Synthesis Using Diisopropylammonium Tetrazole

Used Chemicals

Procedure

2-Cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite (0.7 mL, 2.2 mmol, 1.2 eq.) was added to a solution of DMT-T (1.0 g, 1.8 mmol) and diisopropylammonium tetrazole (160 mg, 0.92 mmol, 0.5 eq.) in dichloromethane (9.2 mL) at room temperature. After the completion of the reaction, saturated aq. NaHCO3 (5 mL) was added to the solution and extracted with dichloromethane (15 mL, twice). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (hexane:ethyl acetate = 70:30 - 50:50, 2% of triethylamine was added to the eluents) to give 1 (1.2 g, 88% yield) as a white crystal.

Experimenter’s Comments

The reaction solution was monitored by NMR.

Analytical Data

Compound 1

1H NMR (400 MHz, CDCl3); δ 11.36 (s, 1H), 7.50 (d, J = 4.0 Hz, 1H), 7.36-7.20 (m, 9H), 6.87-6.83 (m, 4H), 6.16-6.15 (m, 1H), 4.56-4.49 (m, 1H), 3.99 (d, J = 4.0 Hz, 1H), 3.73-3.72 (m, 1H), 3.22-3.19 (m, 1H), 2.72 (t, J = 8.0 Hz, 1H), 2.62 (t, J = 1.2 Hz, 1H), 2.41-2.31 (m, 1H), 1.44 (d, J = 1.2 Hz, 3H), 1.18-1.06 (m, 12H).

Lead Reference

Other Reference


Product Documents (Note: Some products will not have analytical charts available.)
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