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线性分子式:
(CH3)2CHNH2
化学文摘社编号:
分子量:
59.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
200-860-9
Beilstein/REAXYS Number:
605259
MDL number:
InChI key
JJWLVOIRVHMVIS-UHFFFAOYSA-N
InChI
1S/C3H9N/c1-3(2)4/h3H,4H2,1-2H3
SMILES string
CC(C)N
grade
analytical standard
vapor density
2.04 (vs air)
vapor pressure
9.2 psi ( 20 °C)
autoignition temp.
755 °F
quality
anhydrous
shelf life
limited shelf life, expiry date on the label
expl. lim.
10.4 %
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
33-34 °C (lit.)
density
0.688 g/mL at 20 °C (lit.)
application(s)
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care
format
neat
storage temp.
2-8°C
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 1 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
<-13.0 °F - closed cup
flash_point_c
<= -25 °C - closed cup
ppe
Faceshields, Gloves, Goggles
法规信息
危险化学品
此项目有
Comparative effects of the formulation of glyphosate-surfactant herbicides on hemodynamics in swine.
Hsin-Ling Lee et al.
Clinical toxicology (Philadelphia, Pa.), 47(7), 651-658 (2009-08-12)
Most of the glyphosate-surfactant herbicides (GlySH) are formulated commercial products containing isopropylamine (IPA) salt of glyphosate (IPAG), variable amount of a surfactant, and water. Although glyphosate is only slightly toxic to rats, ingestion of GlySH may lead to severe effects
Jacek Lipok et al.
Ecotoxicology and environmental safety, 73(7), 1681-1688 (2010-09-04)
The toxicity of commercial formulation of Roundup® 360 SL, widely used, nonselective herbicide and its main constituents, glyphosate (PMG), equimolar (1:1) isopropylamine salt of glyphosate (GIPA) and isopropylamine (IPA) was examined towards eight aquatic microphotoautotrophs; seven cyanobacterial strains representing either
Gabriel Vallejos et al.
Bioorganic & medicinal chemistry, 13(14), 4450-4457 (2005-05-24)
The in vitro monoamine oxidase inhibitory (MAOI) activities of 11 heteroarylisopropylamines vis-à-vis MAO-A and MAO-B were described and interpreted in terms of possible interactions with the enzyme active site. Molecular dynamics simulations allowed a comparison between the most active MAO-A
Katrijn De Klerck et al.
Journal of chromatography. A, 1234, 72-79 (2011-12-07)
In chiral supercritical fluid chromatography (SFC), mobile-phase additives are often used to improve enantioseparations and peak shapes. An acidic or basic additive is chosen, depending on the nature of the compound. This work highlights the simultaneous use of the acidic
Karim Engelmark Cassimjee et al.
Chemical communications (Cambridge, England), 46(30), 5569-5571 (2010-05-13)
Enantiopure chiral amines synthesis using omega-transaminases is hindered by an unfavourable equilibrium, but when using isopropylamine as the amine donor the equilibrium can be completely displaced by using a specific dehydrogenase in situ for removal of formed acetone.
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