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Merck
CN

01887

3-氨基-1-丙醇

analytical standard

别名:

3-氨基丙醇

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关于此项目

线性分子式:
HO(CH2)3NH2
化学文摘社编号:
分子量:
75.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-864-4
Beilstein/REAXYS Number:
741855
MDL number:
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产品名称

3-氨基-1-丙醇, analytical standard

InChI key

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

InChI

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

SMILES string

NCCCO

grade

analytical standard

vapor density

2.59 (vs air)

vapor pressure

2.1 mmHg ( 20 °C)

assay

≥99.5% (GC)

autoignition temp.

770 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

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.)

application(s)

environmental

format

neat

Quality Level

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General description

3-氨基-1-丙醇是一种直链伯链烷醇胺。

Other Notes

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hcodes

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

存储类别

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

ppe

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


历史批次信息供参考:

分析证书(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
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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