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MilliporeSigma

128511

2,2,4,4,6,8,8-Heptamethylnonane

98%

Synonym(s):

HMN

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About This Item

Linear Formula:
(CH3)3CCH2CH(CH3)CH2C(CH3)2CH2C(CH3)3
CAS Number:
Molecular Weight:
226.44
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
224-506-8
MDL number:
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Product Name

2,2,4,4,6,8,8-Heptamethylnonane, 98%

InChI key

VCLJODPNBNEBKW-UHFFFAOYSA-N

InChI

1S/C16H34/c1-13(10-14(2,3)4)11-16(8,9)12-15(5,6)7/h13H,10-12H2,1-9H3

SMILES string

CC(CC(C)(C)C)CC(C)(C)CC(C)(C)C

vapor density

7.9 (vs air)

vapor pressure

<1 mmHg ( 20 °C)

assay

98%

form

liquid

refractive index

n20/D 1.439 (lit.)

bp

240 °C (lit.)

density

0.793 g/mL at 25 °C (lit.)

Quality Level

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Application

2,2,4,4,6,8,8-Heptamethylnonane was used to study the effects of loading and aging pyrene in soils. It was also used to study its long term effect on the cell surface hydrophobicity (CSH) of a hexane-degrading Pseudomonas aeruginosa strain and a toluene-degrading Pseudomonas putida strain.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1

supp_hazards

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves


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Kathlyn M Kirkwood et al.
Biodegradation, 19(6), 785-794 (2008-02-27)
Mixed bacterial cultures aerobically transformed decalin (decahydronaphthalene) dissolved in an immiscible carrier phase (heptamethylnonane; HMN) in liquid medium. Conversion was enhanced in the presence of decane, a readily degraded n-alkane, and/or HMN. Four Rhodococcus spp. isolates purified from one of
T Ikeda et al.
Xenobiotica; the fate of foreign compounds in biological systems, 18(11), 1271-1280 (1988-11-01)
1. Exposure of rats to 1% (w/w) of 2,2,4,4,6,8,8-heptamethylnonane in the diet for 2 weeks resulted in marked induction of liver peroxisome proliferation as judged from electron micrography, elevated activities of hepatic catalase (36%), cyanide-insensitive palmitoyl-CoA oxidase (10-fold), carnitine acetyl
J Harder et al.
Biodegradation, 11(1), 55-63 (2001-02-24)
Plant volatile organic compounds are a major carbon source in nature. We studied the degradability of these substances by anaerobic microorganisms in enrichment cultures with representative essential oils as organic substrates and nitrate as electron acceptor. Lemon and pine needle
Paulius Palaima et al.
Orphanet journal of rare diseases, 14(1), 197-197 (2019-08-16)
Charcot-Marie-Tooth (CMT) disease is the most common inherited neuromuscular disorder characterized by wide clinical, genetic and pathomechanistic heterogeneity. Recently, the gene encoding peripheral myelin protein 2 (PMP2) was identified as a novel cause for CMT neuropathy with three mutations that
Fauziah F Rochman et al.
Frontiers in microbiology, 8, 1845-1845 (2017-10-17)
Oil sands process-affected water (OSPW), produced by surface-mining of oil sands in Canada, is alkaline and contains high concentrations of salts, metals, naphthenic acids, and polycyclic aromatic compounds (PAHs). Residual hydrocarbon biodegradation occurs naturally, but little is known about the

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