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239844

Sigma-Aldrich

3-Amino-1-propanol

≥99%

Sinônimo(s):

3-Aminopropyl alcohol

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About This Item

Fórmula linear:
HO(CH2)3NH2
Número CAS:
156-87-6
Peso molecular:
75.11
Beilstein:
741855
Número CE:
205-864-4
Número MDL:
MFCD00008223
Código UNSPSC:
12352100
ID de substância PubChem:
24854393
NACRES:
NA.22

densidade de vapor

2.59 (vs air)

pressão de vapor

2.1 mmHg ( 20 °C)

Ensaio

≥99%

forma

liquid

temperatura de autoignição

770 °F

índice de refração

n20/D 1.4598 (lit.)

pb

184-187 °C (lit.)

pf

10-12 °C (lit.)

solubilidade

water: soluble

densidade

0.982 g/mL at 20 °C (lit.)

cadeia de caracteres SMILES

NCCCO

InChI

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

chave InChI

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

3-Amino-1-propanol was used in the synthesis of di-tert-butyl aminopropanol derivative.

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H302,H314

Classificações de perigo

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

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

212.0 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

100 °C - Pensky-Martens closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

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(±)-1-Amino-2-propanol analytical standard

Supelco

95343

(±)-1-Amino-2-propanol

(S)-(+)-2-Amino-1-propanol 98%

Sigma-Aldrich

A76206

(S)-(+)-2-Amino-1-propanol

3-(Boc-amino)-1-propanol 97%

Sigma-Aldrich

416444

3-(Boc-amino)-1-propanol

N-(3-Hydroxypropyl)acetamide AldrichCPR

Sigma-Aldrich

OTV000276

N-(3-Hydroxypropyl)acetamide

Rahul S Kalhapure et al.
International journal of pharmaceutics, 425(1-2), 9-18 (2012-01-24)
There is increasing demand for lipids owing to their use in formulating lipid based drug delivery systems of poorly soluble drugs. The present work discusses the synthesis, characterization of oleic acid based heterolipid and its use as oil in the
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
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