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Merck
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주요 문서

01887

Supelco

3-Amino-1-propanol

analytical standard

동의어(들):

3-Aminopropyl alcohol

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About This Item

Linear Formula:
HO(CH2)3NH2
CAS Number:
Molecular Weight:
75.11
Beilstein:
741855
EC Number:
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

vapor density

2.59 (vs air)

vapor pressure

2.1 mmHg ( 20 °C)

분석

≥99.5% (GC)

autoignition temp.

770 °F

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

refractive index

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

bp

184-187 °C (lit.)

mp

10-12 °C (lit.)

density

0.982 g/mL at 20 °C (lit.)

응용 분야

environmental

형식

neat

SMILES string

NCCCO

InChI

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

InChI key

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

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일반 설명

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

추천 제품

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

픽토그램

CorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point (°F)

212.0 °F - Pensky-Martens closed cup

Flash Point (°C)

100 °C - Pensky-Martens closed cup

개인 보호 장비

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


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

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
Adel A A Emara et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 592-604 (2007-02-27)
The bifunctional carbonyl compound; 4,6-diacetylresorcinol (DAR) serves as precursor for the formation of different Schiff base ligands, which are either di- or tetra-basic with two symmetrical sets of either O2N or N2O tridentate chelating sites. The condensation of 4,6-diacetylresorcinol with

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