产品名称
二异丙胺, 99%
InChI key
UAOMVDZJSHZZME-UHFFFAOYSA-N
InChI
1S/C6H15N/c1-5(2)7-6(3)4/h5-7H,1-4H3
SMILES string
CC(C)NC(C)C
vapor density
3.5 (vs air)
vapor pressure
50 mmHg ( 20 °C)
assay
99%
form
liquid
autoignition temp.
599 °F
expl. lim.
8.5 %
availability
available only in EU
Quality Level
refractive index
n20/D 1.392 (lit.)
bp
84 °C (lit.)
mp
−61 °C (lit.)
solubility
water: soluble 110 g/L at 25 °C
density
0.722 g/mL at 25 °C (lit.)
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
7.8 °F - closed cup
flash_point_c
-13.45 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Synthesis of high carbon materials from acetylenic precursors. Preparation of aromatic monomers bearing multiple ethynyl groups.
Neenan TX and Whitesides GM.
The Journal of Organic Chemistry, 53(11), 2489-2496 (1988)
Reaction of amines and acid catalysts. IV. Kinetics and mechanism of olefin formation from triethylamine and diisopropylamine on ?-alumina.
Hogan P and Pasek J.
Collection of Czechoslovak Chemical Communications, 38(5), 1513-1521 (1973)
Songping Liao et al.
Journal of the American Chemical Society, 125(49), 15114-15127 (2003-12-05)
Lithium diisopropylamide-mediated lithiations of N-alkyl ketimines derived from cyclohexanones reveal that simple substitutions on the N-alkyl side chain and the 2-position of the cyclohexyl moiety afford a 60,000-fold range of rates. Detailed rate studies implicate monosolvated monomers at the rate-limiting
Alexander C Hoepker et al.
The Journal of organic chemistry, 76(19), 7985-7993 (2011-09-06)
Density functional theory computations [MP2/6-31G(d)//B3LYP/6-31G(d)] on the deaggregation of lithium diisopropylamide (LDA) dimer solvated by two tetrahydrofuran ligands to give the corresponding trisolvated monomer show eight structurally distinct minima. The barriers to exchange are comparable to those expected from experimental
Liyan Qiu et al.
Molecular pharmaceutics, 9(5), 1109-1117 (2012-04-13)
pH-responsive drug carriers derived from polymers containing weak base groups have been shown to improve the antitumor effect of chemotherapeutics. The common interpretation is that a "proton sponge effect" caused by pH-responsive polymers facilitates endosomal membrane destruction and accelerates cytoplasmic
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