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About This Item
Linear Formula:
(CH3)2CHNHCH(CH3)2
CAS Number:
Molecular Weight:
101.19
UNSPSC Code:
12352116
EC Index Number:
203-558-5
NACRES:
NA.22
MDL number:
Assay:
≥99% (GC)
Grade:
synthesis grade
Bp:
83-84 °C/1013 hPa
Vapor pressure:
93.33 hPa ( 20 °C)
grade
synthesis grade
Quality Segment
vapor pressure
93.33 hPa ( 20 °C)
assay
≥99% (GC)
form
liquid
autoignition temp.
295 °C
potency
420 mg/kg LD50, oral (Rat), 2900 mg/kg LD50, skin (Rabbit)
expl. lim.
1.1-7.1 % (v/v)
dilution
(for synthesis)
pH
11.8 (20 °C, 6 g/L in H2O)
bp
83-84 °C/1013 hPa
mp
-70 °C
transition temp
flash point -13.45 °C (DIN 51755 Part 1)
density
0.72 g/cm3 at 20 °C
storage temp.
2-30°C
SMILES string
N(C(C)C)C(C)C
InChI
1S/C6H15N/c1-5(2)7-6(3)4/h5-7H,1-4H3
InChI key
UAOMVDZJSHZZME-UHFFFAOYSA-N
General description
Diisopropylamine (DIPA) is an aliphatic secondary amine commonly used as an organic base in chemical synthesis.
Application
Diisopropylamine can be used as:
It can also be used as a starting material to prepare lithium diisopropylamide (LDA), a strong non-nucleophilic base widely used in organic synthesis for deprotonation reactions.
- A reagent to synthesize furan, dihydrofuran, or butanolide derivatives by reacting with γ-ketothioesters.
- A catalyst to prepare aryl disulfides via oxidative coupling of aryl thiols in the presence of air as an oxidant.
- A base in Pd-catalyzed cross-coupling reactions such as Heck and Sonogashira reaction.
It can also be used as a starting material to prepare lithium diisopropylamide (LDA), a strong non-nucleophilic base widely used in organic synthesis for deprotonation reactions.
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Signal Word
Danger
Target Organs
Respiratory system
Storage Class
3 - Flammable liquids
Flash Point (°F)
7.8 °F - closed cup
Flash Point (°C)
-13.45 °C - closed cup
Hazard Codes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - PMT - Repr. 1B - Skin Corr. 1B - STOT SE 3 - vPvM
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