W396508
DL-1-氨基-2-丙醇
≥90%
别名:
(±)-1-氨基-2-丙醇, (±)-异丙醇胺
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关于此项目
线性分子式:
CH3CH(OH)CH2NH2
化学文摘社编号:
分子量:
75.11
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3965
EC Number:
201-162-7
MDL number:
Beilstein/REAXYS Number:
605275
Organoleptic:
fishy
Biological source:
synthetic
Food allergen:
no known allergens
SMILES string
CC(O)CN
InChI key
HXKKHQJGJAFBHI-UHFFFAOYSA-N
InChI
1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3
biological source
synthetic
reg. compliance
FDA 21 CFR 117
vapor density
2.6 (vs air)
vapor pressure
<1 mmHg ( 20 °C)
assay
≥90%
impurities
<10% 2-amino-1-propanol
refractive index
n20/D 1.4478 (lit.)
bp
160 °C (lit.)
mp
−2 °C (lit.)
density
0.973 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
fishy
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
[Substantiation of maximum permissible levels of mono-, di- and triisopropanolamine in the air of work areas].
E N Burkatskaia et al.
Gigiena truda i professional'nye zabolevaniia, (7)(7), 46-48 (1986-07-01)
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
Steven B Hawthorne et al.
Environmental science & technology, 39(10), 3639-3645 (2005-06-15)
Soil and groundwater samples were collected at the site of a former chemical processing plant in areas impacted by accidental releases of MEA (monoethanolamine) and IPA (2-propanolamine or isopropanolamine). Although their use had ceased ca. 10 years before sample collection
J W Davis et al.
Reviews of environmental contamination and toxicology, 149, 87-137 (1997-01-01)
This review provides a summary of current information available on the environmental fate and aquatic toxicology of the alkanolamines. Because these materials are widely used, there is a need to understand their fate and effects in the environment. This assessment
S W Graves et al.
The Journal of biological chemistry, 255(15), 7444-7448 (1980-08-10)
Ethanolamine ammonia-lyase catalyzes the adenosylcobalamin (AdoCbl)-dependent deamination of 1-amino-3-propanol (isopropanolamine) to acetone and NH3. During the course of the reaction a hydrogen is transferred from the carbinol carbon of the substrate to one of the methyl carbons of the product
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