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D161292

Sigma-Aldrich

2-Amino-6-methylheptane

99%

Synonym(s):

1,5-Dimethylhexylamine, 6-Methyl-2-heptylamine

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About This Item

Linear Formula:
(CH3)2CH(CH2)3CH(CH3)NH2
CAS Number:
543-82-8
Molecular Weight:
129.24
Beilstein/REAXYS Number:
1209250
EC Number:
208-851-1
MDL number:
MFCD00008092
UNSPSC Code:
12352100
PubChem Substance ID:
24893495
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.422 (lit.)

bp

154-156 °C (lit.)

density

0.767 g/mL at 25 °C (lit.)

SMILES string

CC(C)CCCC(C)N

InChI

1S/C8H19N/c1-7(2)5-4-6-8(3)9/h7-8H,4-6,9H2,1-3H3

InChI key

QNIVIMYXGGFTAK-UHFFFAOYSA-N

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Application

2-Amino-6-methylheptane can be used as:
  • A building block for the synthesis of n-type photoconductor, N,N′-bis(1,5-dimethylhexyl)-3,4:9,10-perylenebis (dicarbox-imide) (PDHEP).
  • A reagent in the synthesis of substituted pyrrolidones by reductive amination of levulinic acid using supported platinum catalyst.
  • A nucleophilic amine in the synthesis of unsymmetrical sulfamide by reacting with sulfamic acid salts and triphenylphosphine ditriflate.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

118.4 °F - closed cup

flash_point_c

48 °C - closed cup

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Microwave-assisted synthesis of phthalocyanine-porphyrin complex and its photoelectric conversion properties
Liu MO and Hu AT
Journal of Organometallic Chemistry, 689(15), 2450-2455 (2004)
Heterogeneous Pt catalysts for reductive amination of levulinic acid to pyrrolidones
Touchy AS, et al.
ACS Catalysis, 4(9), 3045-3050 (2014)
Efficient synthesis of unsymmetrical sulfamides from sulfamic acid salts by activation with triphenylphosphine ditriflate
Shehata MF, et al.
Tetrahedron, 75(24), 3186-3194 (2019)
Pieter A Cohen et al.
Clinical toxicology (Philadelphia, Pa.), 56(6), 421-426 (2017-11-09)
The United States Food and Drug Administration banned the stimulant 1,3-dimethylamylamine (1,3-DMAA) from dietary supplements and warned consumers that the stimulant can pose cardiovascular risks ranging from high blood pressure to heart attacks. We designed our study to determine if

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