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126802

Sigma-Aldrich

Heptylamine

99%

Sinónimos:

1-Aminoheptane

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About This Item

Fórmula lineal:
CH3(CH2)6NH2
Número de CAS:
111-68-2
Peso molecular:
115.22
Beilstein/REAXYS Number:
1731688
EC Number:
203-895-8
MDL number:
MFCD00008244
UNSPSC Code:
12352100
PubChem Substance ID:
24847743
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.424 (lit.)

bp

154-156 °C (lit.)

density

0.777 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCN

InChI

1S/C7H17N/c1-2-3-4-5-6-7-8/h2-8H2,1H3

InChI key

WJYIASZWHGOTOU-UHFFFAOYSA-N

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Application

Heptylamine has been used as an internal standard in the determination of biogenic monoamines and biogenic diamines by the fluorescence-HPLC method. It has also been used to study the effect of hydration on the gaseous structure of protonated heptylamine by infrared photodissociation (IRPD) spectroscopy and computational chemistry.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

111.2 °F - closed cup

flash_point_c

44 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Decylamine ≥99.0% (GC)

Sigma-Aldrich

30692

Decylamine

Tetradecylamine 95%

Sigma-Aldrich

T10200

Tetradecylamine

2-Aminoheptane for synthesis

Sigma-Aldrich

8.41027

2-Aminoheptane

N-Hexylmethylamine 96%

Sigma-Aldrich

359327

N-Hexylmethylamine

Polina Bogdanova et al.
Talanta, 216, 120992-120992 (2020-05-28)
A phenomenon of supramolecular solvents formation in aqueous solutions containing primary amine and monoterpenoid compound is presented for the first time. A novel supramolecular solvent-based liquid phase microextraction was developed. In an aqueous phase primary amine formed isotropic solution due
Ksenia Cherkashina et al.
Analytica chimica acta, 1074, 117-122 (2019-06-05)
A homogeneous liquid-liquid microextraction procedure based on primary amine phase separation was developed as a novel approach for the pretreatment of biological fluids. The procedure assumes primary amine dissolution in the aqueous sample phase, resulting in the creation of a
Dalin Ly et al.
Foods (Basel, Switzerland), 9(2) (2020-02-23)
Naturally fermented foods are an important part of the typical diet in Cambodia. However, the food safety status of these products has not been widely studied. The aim of this study was, therefore, to provide an overview of the quality
Dibyangana Parbat et al.
Chemical science, 8(9), 6092-6102 (2017-10-11)
Bioinspired underwater super-oil-wettability (superoleophilic/superoleophobic) properties are emerging as a potential avenue for developing smart materials for addressing issues related to healthcare, environment, energy
Maria Demireva et al.
Journal of the American Chemical Society, 134(27), 11216-11224 (2012-06-20)
Effects of hydration on the gaseous structures of diprotonated 1,7-diaminoheptane and protonated heptylamine are investigated by infrared photodissociation (IRPD) spectroscopy and computational chemistry. IRPD spectra in the hydrogen bond stretching region (2800-3900 cm(-1)) indicate that 1,7-diammoniumheptane is linear and that
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