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A56205

Sigma-Aldrich

2-Aminoheptane

99%

Synonym(s):

1-Methylhexylamine, 2-Heptylamine

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About This Item

Linear Formula:
CH3(CH2)4CH(NH2)CH3
CAS Number:
123-82-0
Molecular Weight:
115.22
Beilstein/REAXYS Number:
635676
EC Number:
204-655-5
MDL number:
MFCD00008101
UNSPSC Code:
12352100
PubChem Substance ID:
24891001
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.418 (lit.)

bp

142-144 °C (lit.)

density

0.766 g/mL at 25 °C (lit.)

SMILES string

CCCCCC(C)N

InChI

1S/C7H17N/c1-3-4-5-6-7(2)8/h7H,3-6,8H2,1-2H3

InChI key

VSRBKQFNFZQRBM-UHFFFAOYSA-N

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Application

2-Aminoheptane is a secondary alkyl amine that can be used to synthesize 3-amino-2-heptanone hydrochloride.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000173255
0000164889
STBK5793
0000143945
0000139949

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Mahir Tursun et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 114, 668-680 (2013-07-05)
FT-IR and Raman spectra of 1-heptylamine (1-ha) have been recorded in the region of 4000-10 cm(-1) and 4000-50 cm(-1), respectively. The conformational analysis, optimized geometric parameters, normal mode frequencies and corresponding vibrational assignments of 1-ha (C7H17N) have been examined by
Reactions of Amines. V. Synthesis of ?-Amino Ketones1, 2.
Baumgarten HE
Journal of the American Chemical Society, 82(2), 459-463 (1960)
Mario Thevis et al.
Rapid communications in mass spectrometry : RCM, 31(15), 1290-1296 (2017-05-17)
Continuously refining and advancing the strategies and methods employed in sports drug testing is critical for efficient doping controls. Besides improving and expanding the spectrum of target analytes, alternative test matrices have warranted in-depth evaluation as they commonly allow for
Christian Görgens et al.
Journal of pharmaceutical and biomedical analysis, 131, 482-496 (2016-10-04)
So far, in sports drug testing compounds of different classes are processed and measured using different screening procedures. The constantly increasing number of samples in doping analysis, as well as the large number of substances with doping related, pharmacological effects
Núria Monfort et al.
Drug testing and analysis, 7(9), 819-830 (2015-03-03)
A fast screening method for the detection of more than 60 stimulants in urine was developed. The method consisted of a dilution of the urine (1:5 v/v) and analysis by ultra high performance liquid chromatography coupled to tandem mass spectrometry

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