192171
DL-丙氨醇
98%
别名:
(±)-2-氨基-1-丙醇
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关于此项目
线性分子式:
CH3CH(NH2)CH2OH
化学文摘社编号:
分子量:
75.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-207-3
Beilstein/REAXYS Number:
1209234
MDL number:
产品名称
DL-丙氨醇, 98%
InChI key
BKMMTJMQCTUHRP-UHFFFAOYSA-N
InChI
1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3
SMILES string
CC(N)CO
assay
98%
form
liquid
optical activity
[α]/D +1.0 to −1.0°
refractive index
n20/D 1.450 (lit.)
bp
173-176 °C (lit.)
density
0.943 g/mL at 25 °C (lit.)
functional group
amine
hydroxyl
Quality Level
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Application
DL-Alaninol has been used in the synthesis of:
- N6-α-(I-hydroxypropyl) lysine
- diastereomers of DL-β-amino alcohols
- enantiopure and racemic samples of 2-methyl-N-tosylaziridine
- (±)-3-(5-dimethylcarbamoyl-pent-1-enyl)-N-(2-hydroxy-1-methyl-ethyl)benzamide
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
183.2 °F - closed cup
flash_point_c
84 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Ian C Stewart et al.
Journal of the American Chemical Society, 127(50), 17616-17617 (2005-12-15)
Sulfonylaziridines have been identified as excellent monomers for living ring-opening polymerization initiated by nucleophilic sulfonylamides. The resulting polymers exhibit low polydispersities and controllable molecular weights. The enantiopurity of the monomer plays a key role: racemic samples yield soluble polymers of
The role of lysine residues in the activity of 2-keto-3-deoxy-6-phosphogluconate aldolase.
J M Ingram et al.
The Journal of biological chemistry, 240(11), 4146-4151 (1965-11-01)
P M Hoi et al.
British journal of pharmacology, 152(5), 751-764 (2007-09-25)
A putative novel cannabinoid receptor mediates vasorelaxation to anandamide and abnormal-cannabidiol and is blocked by O-1918 and by high concentrations of rimonabant. This study investigates VSN16, a novel water-soluble agonist, as a vasorelaxant potentially acting at non-CB1, non-CB2 cannabinoid receptors
Vahe Bandarian et al.
Biochemistry, 41(27), 8580-8588 (2002-07-03)
The structure of the steady-state radical intermediate in the deamination of S-2-aminopropanol catalyzed by ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium has been probed by electron paramagnetic resonance (EPR) spectroscopy using isotopically labeled forms of the substrate and of the adenosylcobalamin
R LoBrutto et al.
Biochemistry, 40(1), 9-14 (2001-01-05)
The mechanism of propagation of the radical center between the cofactor, substrate, and product in the adenosylcobalamin- (AdoCbl) dependent reaction of ethanolamine ammonia-lyase has been probed by pulsed electron nuclear double resonance (ENDOR) spectroscopy. The radical of S-2-aminopropanol, which appears
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