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:
Assay:
98%
Form:
liquid
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.
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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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
Maike F Dohrn et al.
Current opinion in neurology, 33(5), 568-574 (2020-08-17)
Hereditary motor neuropathies (HMN) comprise a broad genotypic and phenotypic spectrum of rare, progressively disabling diseases manifesting with length-dependent muscle weakness and atrophy. To date, more than half of the cases cannot be genetically explained. To provide symptomatic and disease-modifying
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
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
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
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