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3-Amino-1-propanol

analytical standard

Synonym(e):

3-Amino-propylalkohol

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About This Item

Lineare Formel:
HO(CH2)3NH2
CAS-Nummer:
156-87-6
Molekulargewicht:
75.11
Beilstein:
741855
EG-Nummer:
205-864-4
MDL-Nummer:
MFCD00008223
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329747368
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Dampfdichte

2.59 (vs air)

Dampfdruck

2.1 mmHg ( 20 °C)

Assay

≥99.5% (GC)

Selbstzündungstemp.

770 °F

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.4598 (lit.)
n20/D 1.461

bp

184-187 °C (lit.)

mp (Schmelzpunkt)

10-12 °C (lit.)

Dichte

0.982 g/mL at 20 °C (lit.)

Anwendung(en)

environmental

Format

neat

SMILES String

NCCCO

InChI

1S/C3H9NO/c4-2-1-3-5/h5H,1-4H2

InChIKey

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

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Allgemeine Beschreibung

3-Amino-1-propanol is a linear primary alkanolamine.

Empfohlene Produkte

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Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

H-Sätze

H302,H314

Gefahreneinstufungen

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

WGK

WGK 1

Flammpunkt (°F)

212.0 °F

Flammpunkt (°C)

100 °C

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Analysenzertifikate (COA)

Lot/Batch Number

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P Kovács et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 118(1), 83-87 (1997-11-20)
3-Amino-1-propanol (AP), a substance replacing ethanolamine in phosphatidylethanolamine (PE) significantly reduced 32P incorporation to phosphatidylinositol (PI) and glycosyl-phosphatidylinositol (GPI) in the unicellular organism Tetrahymena pyriformis. At 10 mM, AP completely inhibited the incorporation of 32P into PI. 3H-arachidonate incorporation into
Manuela L Kim et al.
Talanta, 77(3), 1068-1074 (2008-12-10)
An hybrid mesoporous material synthesised in our laboratories for solid phase extraction (SPE) in flow through systems has been used for analytical purposes. The solid was obtained from mesoporous silica MCM-41 functionalized with 3-aminopropyltriethoxy silane by Sol-Gel methodology. In order
C Cacela et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56(6), 1051-1064 (2000-06-14)
Results obtained for the isolated and liquid 3-amino-1-propanol by a concerted molecular orbital and vibrational spectroscopic approach are reported. The relative energies and both structural and vibrational data of the different conformers of the studied compound were calculated using the
Thatavarathy Rama Krishna et al.
The Journal of organic chemistry, 68(25), 9694-9704 (2003-12-06)
In this paper, we report the synthesis of several poly(propyl ether imine) dendrons and dendrimers. These dendrons and dendrimers were constructed by involving an ether as the linker component and an imine as the branching component. The divergent syntheses of
Ofer Eidelman et al.
Biochemistry, 41(37), 11161-11170 (2002-09-11)
Cystic fibrosis commonly occurs as a consequence of the DeltaF508 mutation in the first nucleotide binding fold domain (NBF-1) of CFTR. The mutation causes retention of the mutant CFTR molecule in the endoplasmic reticulum, and this aberrant trafficking event is
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