126411
1,3-Dimethylbutylamin
98%
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Alle Fotos(2)
About This Item
Lineare Formel:
(CH3)2CHCH2CH(CH3)NH2
CAS-Nummer:
Molekulargewicht:
101.19
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
98%
Brechungsindex
n20/D 1.4085 (lit.)
bp
108-110 °C (lit.)
Dichte
0.717 g/mL at 25 °C (lit.)
Funktionelle Gruppe
amine
SMILES String
CC(C)CC(C)N
InChI
1S/C6H15N/c1-5(2)4-6(3)7/h5-6H,4,7H2,1-3H3
InChIKey
UNBMPKNTYKDYCG-UHFFFAOYSA-N
Anwendung
1,3-Dimethylbutylamine has been used to study the application of unfunctionized polymethacrylate resin (TSKgel G3000PWXL) as a stationary phase in liquid chromatography with UV detection.
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 3
Flammpunkt (°F)
55.4 °F - closed cup
Flammpunkt (°C)
13 °C - closed cup
Persönliche Schutzausrüstung
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Kazutoku Ohta et al.
Journal of chromatography. A, 1039(1-2), 161-169 (2004-07-15)
The application of unfunctionized polymethacrylate resin (TSKgel G3000PWXL) as a stationary phase in liquid chromatography with UV detection for C1-C7 aliphatic monocarboxylic acids (formic acid, acetic acid, propionic acid, butyric acid, isovaleric acid, valeric acid, 3,3-dimethylbutyric acid, 4-methylvaleric acid, hexanoic
Hong Ren et al.
Journal of biotechnology, 241, 33-41 (2016-11-14)
Asymmetric synthesis of chiral amines by amine dehydrogenases (AmDH), which catalyzed reductive amination of ketones with high enantioselectivity, is an ideal route for production of chiral amine. In this study, a facile approach is proposed to immobilize unstable amine dehydrogenase
Anna Rickli et al.
European journal of pharmacology, 859, 172515-172515 (2019-07-03)
Preworkout supplements ("boosters") are used to enhance physical and mental performance during workouts. These products may contain various chemical substances with undefined pharmacological activity. We investigated whether substances that are contained in commercially available athletic multiple-ingredient preworkout supplements exert amphetamine-type
Pieter A Cohen et al.
Clinical toxicology (Philadelphia, Pa.), 56(6), 421-426 (2017-11-09)
The United States Food and Drug Administration banned the stimulant 1,3-dimethylamylamine (1,3-DMAA) from dietary supplements and warned consumers that the stimulant can pose cardiovascular risks ranging from high blood pressure to heart attacks. We designed our study to determine if
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