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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:
635676
EC Number:
204-655-5
MDL number:
MFCD00008101
UNSPSC Code:
12352100
PubChem Substance ID:
24891001
NACRES:
NA.22

Quality Level

100

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

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000374311
0000328250
SDBB1592
STBL3774
0000342378

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Reactions of Amines. V. Synthesis of ?-Amino Ketones1, 2.
Baumgarten HE
Journal of the American Chemical Society, 82(2), 459-463 (1960)
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
Akash Singh et al.
Advanced materials (Deerfield Beach, Fla.), 33(3), e2005868-e2005868 (2020-12-08)
Crystalline metal halide perovskites (MHPs) have provided unprecedented advances in interdisciplinary fields of materials, electronics, and photonics. While crystallinity offers numerous advantages, the ability to access a glassy state with distinct properties provides unique opportunities to extend the associated structure-property
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
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