Delhiraja, Krithika team published research on Environmental Monitoring and Assessment in 2020 | 24034-73-9

24034-73-9, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.

Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, Safety of (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol

In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 24034-73-9, formula is C20H34O, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Safety of (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol

Delhiraja, Krithika;Philip, Ligy research published 《 Characterization of segregated greywater from Indian households-part B: emerging contaminants》, the research content is summarized as follows. Abstract: Emerging contaminants (ECs) have become an increasing area of concern due to the likely impacts of these compounds on human health and the environment. Generally, products which are used for households and personal care activities contribute to major percentage of ECs in household greywater. Not much information on the presence of xenobiotic organic compounds in greywater is currently available. Therefore, the present study focused on the qual. and quant. analyses of emerging contaminants from different classifications of Indian households. The quant. anal. of few selected target pollutants such as phthalic esters, namely di-Et hexyl phthalate, di-Et phthalate, di-Bu phthalate, dioctyl phthalate, triclosan, bisphenol A, caffeine, acetaminophen, 3-Me salicylic acid, 4-octylphenol, and 4-nonylphenol were found to be 0.38 ± 0.39 μg/L, 1.57 ± 1.54 μg/L, 4.77 ± 2.57 μg/L, 0.712 ± 0.17 μg/L, 5.82 ± 1.85 μg/L, 11.08 ± 2.64 μg/L, 2.30 ± 1.19 μg/L 13.18 ± 4.48 μg/L, 3.75 ± 1.90 μg/L, 4.95 ± 2.21 μg/L, and 5.96 μg/L, resp. Risk assessment indicated that 63 compounds identified in the greywater can be considered priority pollutants. Based on the results obtained in the present study, effective zero-discharge liquid system can be designed for different sources of greywater and it can be recycled and reused without much risk. Graphical abstract [graphic not available: see fulltext]

24034-73-9, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.

Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, Safety of (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts