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Merck
CN

W396508

Sigma-Aldrich

DL-1-Amino-2-propanol

≥90%

Synonym(s):

(±)-1-Amino-2-propanol, (±)-Isopropanolamine

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About This Item

Linear Formula:
CH3CH(OH)CH2NH2
CAS Number:
78-96-6
Molecular Weight:
75.11
FEMA Number:
3965
Beilstein:
605275
EC Number:
201-162-7
MDL number:
MFCD00008139
UNSPSC Code:
12164502
PubChem Substance ID:
329830669
NACRES:
NA.21
Organoleptic:
fishy
Biological source:
synthetic
Food allergen:
no known allergens

Key Documents

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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

SMILES string

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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Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H312,H314

Hazard Classifications

Acute Tox. 4 Dermal - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

159.8 °F - closed cup

Flash Point(C)

71 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBH4318
STBG3743V
STBD1321V
STBC9806V
STBC4984V

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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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