192171
DL-アラニノール
98%
別名:
(±)-2-アミノ-1-プロパノール
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この商品について
化学式:
CH3CH(NH2)CH2OH
CAS番号:
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:
Assay:
98%
Form:
liquid
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°
Quality Level
bp
173-176 °C (lit.)
density
0.943 g/mL at 25 °C (lit.)
functional group
amine, hydroxyl
関連するカテゴリー
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
保管分類
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
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
第4類:引火性液体 + 第三石油類 + 危険等級III + 非水溶性液体
fsl
192171-VAR: + 192171-25G: + 192171-5G: + 192171-BULK:
jan
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
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)
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
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
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
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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