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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:
1209250
EC Number:
208-851-1
MDL number:
MFCD00008092
UNSPSC Code:
12352100
PubChem Substance ID:
24893495
NACRES:
NA.22

Quality Level

100

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

Signal Word

Warning

Hazard Statements

H226,H302,H315,H319

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

118.4 °F

Flash Point(C)

48 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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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Heterogeneous Pt catalysts for reductive amination of levulinic acid to pyrrolidones
Touchy AS, et al.
ACS Catalysis, 4(9), 3045-3050 (2014)
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)
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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