8.00894
N-Ethyldiisopropylamine
for synthesis
Synonym(s):
N-Ethyldiisopropylamine, N,N-Diisopropylethylamine
Select a Size
About This Item
Product Name
N-Ethyldiisopropylamine, for synthesis
SMILES string
N(C(C)C)(C(C)C)CC
InChI
1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3
InChI key
JGFZNNIVVJXRND-UHFFFAOYSA-N
grade
synthesis grade
vapor pressure
14 hPa ( 20 °C)
assay
≥98% (GC)
form
liquid
autoignition temp.
240 °C
potency
200-500 mg/kg LD50, oral (Rat)
expl. lim.
0.7-6.3 % (v/v)
dilution
(for synthesis)
pH
12.3 (20 °C in H2O, as an emulsion)
kinematic viscosity
0.88 cSt(20 °C)
bp
127 °C/1013 hPa
transition temp
flash point 9.5 °C
density
0.76 g/cm3 at 20 °C
storage temp.
2-30°C
Quality Level
Analysis Note
Density (d 20 °C/ 4 °C): 0.755 - 0.758
Water (K. F.): ≤ 0.20 %
Identity (IR): passes test
Application
- Dual Stimuli-Responsive Hybrid Polymeric Nanoparticles Self-Assembled from POSS-Based: Describes the synthesis of hybrid polymeric nanoparticles using N-Ethyldiisopropylamine in the assembly process (Yang et al., 2022).
- Magnetical Control of the Charge-Separated State Lifetime Realized by Covalent Attachment of a Platinum Complex: Details the use of N-Ethyldiisopropylamine in the preparation of magnetically controllable platinum complexes (Kozaki et al., 2021).
- Hybrid block copolymers of polyesters/polycarbonates and polypeptides synthesized via one-pot sequential ring-opening polymerization: Explains the initiation of polymerization with N-Ethyldiisopropylamine for creating hybrid block copolymers (Gradišar et al., 2018).
General description
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
49.1 °F
flash_point_c
9.5 °C
Regulatory Information
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Protocols
Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service