Mono-o-(phytanyl)pentaerythritol → mono-O-(phytanyl)pentaerythritol water

HRID 2260961Notes

Reaction equation

HRID 2260961 reaction equation
[CH3:1][CH:2]([CH2:14][CH2:15][CH2:16][CH:17]([CH3:29])[CH2:18][CH2:19][CH2:20][CH:21]([CH3:28])[CH2:22][CH2:23][CH2:24][CH:25]([CH3:27])[CH3:26])[CH2:3][CH2:4][O:5][CH2:6][C:7]([CH2:12][OH:13])([CH2:10][OH:11])[CH2:8][OH:9]>O>[CH2:4]([O:5][CH2:6][C:7]([CH2:12][OH:13])([CH2:10][OH:11])[CH2:8][OH:9])[CH2:3][CH:2]([CH2:14][CH2:15][CH2:16][CH:17]([CH2:18][CH2:19][CH2:20][CH:21]([CH2:22][CH2:23][CH2:24][CH:25]([CH3:26])[CH3:27])[CH3:28])[CH3:29])[CH3:1].[OH2:5]

Participants

3

Reactant 1

HCID 11697364Mono-o-(phytanyl)pentaerythritol2×

Product 1

HCID 131728552mono-O-(phytanyl)pentaerythritol water

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Mono-O-(3,7,11,15-tetramethylhexadecyl)pentaerythritol (hereafter referred to as “mono-O-(phytanyl)pentaerythritol,” formula (5) above) and pure water were introduced into a mixing device, and incubation was carried out while performing 100 or more times of mixing operations at room temperature (23° C.) over the period of 48 hours. Thus, a homogeneously mixed sample of mono-O-(phytanyl)pentaerythritol/water system was obtained. This sample of mono-O-(phytanyl)pentaerythritol/water system appeared to be a transparent gel composition.

Workup

  1. additionwere introduced into a mixing device, and incubation
  2. customat room temperature
  3. custom(23° C.)
  4. customover the period of 48 hours

Sources & evidence

ORD record
ord-276a3bf05fac476a9c3dfd9492cb1a69
Source dataset
uspto-grants-2010_12
Patent number
US07846903B2

Reaction notes

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