W396508
DL-1-氨基-2-丙醇
≥90%
别名:
(±)-1-氨基-2-丙醇, (±)-异丙醇胺
生物来源
synthetic
管理合规性
FDA 21 CFR 117
蒸汽密度
2.6 (vs air)
蒸汽压
<1 mmHg ( 20 °C)
方案
≥90%
杂质
<10% 2-amino-1-propanol
折射率
n20/D 1.4478 (lit.)
沸点
160 °C (lit.)
mp
−2 °C (lit.)
密度
0.973 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
fishy
SMILES字符串
CC(O)CN
InChI
1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3
InChI key
HXKKHQJGJAFBHI-UHFFFAOYSA-N
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警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Dermal - Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
159.8 °F - closed cup
闪点(°C)
71 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Ravi Bhushan et al.
Journal of chromatography. A, 1216(45), 7941-7945 (2009-10-06)
Taking into account the structural similarities of amino alcohols with amino acids and in order to reduce time for derivatization unconventional approaches viz. microwave irradiation, ultrasonication and ultra centrifugation were applied for synthesis of dinitrophenyl derivatives of nine amino alcohols
Contact allergy to isopropanolamine in Traxam gel.
S M Cooper et al.
Contact dermatitis, 41(4), 233-234 (1999-10-09)
S H Ford
Biochimica et biophysica acta, 841(3), 306-317 (1985-09-06)
Two intermediate stages in cobalamin biosynthesis, amidation of carboxylic acid groups in the corrin ring and (R)-1-amino-2-propanol attachment at propionic acid position f, have been studied using cell-free extracts from the obligate anaerobe Clostridium tetanomorphum. The preparation of an incomplete
Lijun Zhou et al.
Chemical & pharmaceutical bulletin, 56(8), 1147-1152 (2008-08-02)
Novel potential human immunodeficiency virus (HIV) protease inhibitors were designed by a combination of nelfinavir and amprenavir motifs. The designed compounds were prepared by a facile synthetic route and their stereochemistry was further confirmed by a stereospecific synthesis from commercially
Roberto Di Santo et al.
Bioorganic & medicinal chemistry, 10(8), 2511-2526 (2002-06-12)
A series of N-aryl heteroarylisopropanolamines in which an indole or a 3-arylpyrrole moiety was linked to an aryl group through an isopropanolamine linker, were designed and synthesized as potential anti-HIV-1-PR agents. Series was tested for their ability in blocking PR
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