추천 제품
vapor density
3.5 (vs air)
Quality Level
vapor pressure
50 mmHg ( 20 °C)
분석
≥99.5%
형태
liquid
autoignition temp.
599 °F
expl. lim.
8.5 %
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.)
SMILES string
CC(C)NC(C)C
InChI
1S/C6H15N/c1-5(2)7-6(3)4/h5-7H,1-4H3
InChI key
UAOMVDZJSHZZME-UHFFFAOYSA-N
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일반 설명
Diisopropylamine (DIPA) is an aliphatic secondary amine widely used as an organic base in organic synthesis. Its standard molar enthalpy of formation and combustion has been measured by static-bomb calorimetry.
애플리케이션
Diisopropylamine (DIPA) may be used in the following syntheses:
- diisopropylamine methyl urea (DMU)
- N,N-diisopropyl quinoline-2-carboxamide
- 3-N-sulfonylamidine coumarins
- N-chloroamine, an intermediate to generate amides
신호어
Danger
유해 및 위험 성명서
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
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
7.8 °F - closed cup
Flash Point (°C)
-13.45 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
이미 열람한 고객
Iron-Catalyzed Direct Synthesis of Amides from Methylarenes.
Advanced Synthesis & Catalysis, 357(7), 1437-1445 (2015)
A simple and novel amide ligand based on quinoline derivative used for palladium-catalyzed Suzuki coupling reaction.
Journal of Organometallic Chemistry, 794, 27-32 (2015)
Enthalpies of combustion of di-n-propylamine, diisopropylamine, diisobutylamine, and di-sec-butylamine.
The Journal of Chemical Thermodynamics, 29(9), 1025-1030 (1997)
Microwave-Assisted Copper-Catalyzed Four Component Tandem Synthesis of 3-N-Sulfonylamidine Coumarins.
The Journal of Organic Chemistry, 80 (12), 6291-6299 (2015)
Research on Synthesis and Corrosion Inhibitory Performance of Diisopropylamine Methyl Urea.
Applied Mechanics and Materials, 713, 2839-2842 (2015)
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