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Merck
CN

53646

Propylamine

analytical standard

Synonym(s):

1-Aminopropane

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About This Item

Linear Formula:
CH3CH2CH2NH2
CAS Number:
107-10-8
Molecular Weight:
59.11
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329757964
EC Number:
203-462-3
Beilstein/REAXYS Number:
1098243
MDL number:
MFCD00008205

Key Documents

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Product Name

Propylamine, analytical standard

InChI

1S/C3H9N/c1-2-3-4/h2-4H2,1H3

InChI key

WGYKZJWCGVVSQN-UHFFFAOYSA-N

SMILES string

CCCN

grade

analytical standard

vapor density

2 (vs air)

vapor pressure

4.79 psi ( 20 °C)

assay

≥99.0% (GC)

autoignition temp.

604 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

10.4 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤1.0% water

refractive index

n20/D 1.387-1.389
n20/D 1.388 (lit.)

bp

48 °C (lit.)

mp

−83 °C (lit.)

density

0.719 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

<-31.0 °F

flash_point_c

< -35 °C

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5249
BCCH0969
BCCD2233
BCCC3387
BCBV4333

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Ryan R Gordon et al.
PloS one, 9(9), e104271-e104271 (2014-09-10)
To identify molecular alterations in prostate cancers associating with relapse following neoadjuvant chemotherapy and radical prostatectomy patients with high-risk localized prostate cancer were enrolled into a phase I-II clinical trial of neoadjuvant chemotherapy with docetaxel and mitoxantrone followed by prostatectomy.
Sebastian Finger et al.
Biological chemistry, 395(7-8), 769-778 (2014-07-09)
The binding of cationic polyamines to negatively charged lipid membranes is driven by electrostatic interactions and additional hydrophobic contributions. We investigated the effect of polyamines with different number of charges and charge separation on the phase transition behavior of vesicles
Claire Bagnéris et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(23), 8428-8433 (2014-05-23)
Voltage-gated sodium channels are important targets for the development of pharmaceutical drugs, because mutations in different human sodium channel isoforms have causal relationships with a range of neurological and cardiovascular diseases. In this study, functional electrophysiological studies show that the
Lionel Faure et al.
Phytochemistry, 110, 58-71 (2014-12-11)
Alkamides and N-acylethanolamines (NAEs) are bioactive, amide-linked lipids that influence plant development. Alkamides are restricted to several families of higher plants and some fungi, whereas NAEs are widespread signaling molecules in both plants and animals. Fatty acid amide hydrolase (FAAH)
István Ilisz et al.
Journal of pharmaceutical and biomedical analysis, 98, 130-139 (2014-06-09)
Procedures for the direct high-performance liquid chromatographic enantiomer separation of four bicyclo[2.2.2]octane-based 3-amino-2-carboxylic acids were developed in polar-ionic mode on zwitterionic chiral stationary phases (CSPs) based on cinchonane alkaloide quinine, quinidine and chiral sulfonic acid motifs. The effects of the
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