C07C46/10

Novel Methods For Processing Lignocellulosic Material
20190390405 · 2019-12-26 ·

The invention relates to novel methods for processing lignocellulosic material. More specifically, the invention proves an integrated approach for processing cellulose to obtain paper and pulp and valorizing lignin to obtain value-added chemicals and products.

Novel Methods For Processing Lignocellulosic Material
20190390405 · 2019-12-26 ·

The invention relates to novel methods for processing lignocellulosic material. More specifically, the invention proves an integrated approach for processing cellulose to obtain paper and pulp and valorizing lignin to obtain value-added chemicals and products.

CO-CRYSTAL OF COENZYME QH AND NICOTINAMIDE, PREPARATION METHOD THEREFOR AND USE THEREOF
20240140897 · 2024-05-02 ·

The present invention relates to a co-crystal of coenzyme QH and nicotinamide, a preparation method therefor and the use thereof. Compared with the existing coenzyme QH, the co-crystal has a higher melting point and superior stability. The preparation method for the co-crystal of coenzyme QH is simple, easy to control and good in terms of reproducibility. The present invention greatly improves the use convenience of coenzyme QH, saves costs during storage, transportation and use, and broadens the application range of coenzyme QH.

CO-CRYSTAL OF COENZYME QH AND NICOTINAMIDE, PREPARATION METHOD THEREFOR AND USE THEREOF
20240140897 · 2024-05-02 ·

The present invention relates to a co-crystal of coenzyme QH and nicotinamide, a preparation method therefor and the use thereof. Compared with the existing coenzyme QH, the co-crystal has a higher melting point and superior stability. The preparation method for the co-crystal of coenzyme QH is simple, easy to control and good in terms of reproducibility. The present invention greatly improves the use convenience of coenzyme QH, saves costs during storage, transportation and use, and broadens the application range of coenzyme QH.

Process for preparing a <i>Lawsonia inermis </i>extract

The present disclosure relates to a process for preparing a Lawsonia inermis extract which is rich in Lawsone. It also relates to the extract which may be obtained by said process and to a composition comprising thereof. The disclosure also relates to a method for dying fibers, in particular keratin fibers.

Process for preparing a <i>Lawsonia inermis </i>extract

The present disclosure relates to a process for preparing a Lawsonia inermis extract which is rich in Lawsone. It also relates to the extract which may be obtained by said process and to a composition comprising thereof. The disclosure also relates to a method for dying fibers, in particular keratin fibers.

PRODUCTION METHOD FOR REDUCED COENZYME Q10 FORM-II TYPE CRYSTAL OR CRYSTALLINE SOLID THEREOF

It is an object of the present disclosure to provide a method for producing a reduced coenzyme Q10 Form II crystal or a crystalline solid thereof, which is excellent in the filterability of a slurry containing a reduced coenzyme Q10 Form II crystal.

The present embodiment is a method for producing a reduced coenzyme Q10 Form II crystal or a crystalline solid thereof, including: adding a reduced coenzyme Q10 Form II crystal as a seed crystal to a mixed solution containing an alcohol and a reduced coenzyme Q10; and precipitating a reduced coenzyme Q10 Form II crystal in the mixed solution after adding the seed crystal, wherein a change rate of formazin turbidity (FTU) is maintained at 15 FTU/min or more for 80% or more of a period during which the formazin turbidity (FTU) shifts from 1,000 to 10,000 in the precipitation.

PRODUCTION METHOD FOR REDUCED COENZYME Q10 FORM-II TYPE CRYSTAL OR CRYSTALLINE SOLID THEREOF

It is an object of the present disclosure to provide a method for producing a reduced coenzyme Q10 Form II crystal or a crystalline solid thereof, which is excellent in the filterability of a slurry containing a reduced coenzyme Q10 Form II crystal.

The present embodiment is a method for producing a reduced coenzyme Q10 Form II crystal or a crystalline solid thereof, including: adding a reduced coenzyme Q10 Form II crystal as a seed crystal to a mixed solution containing an alcohol and a reduced coenzyme Q10; and precipitating a reduced coenzyme Q10 Form II crystal in the mixed solution after adding the seed crystal, wherein a change rate of formazin turbidity (FTU) is maintained at 15 FTU/min or more for 80% or more of a period during which the formazin turbidity (FTU) shifts from 1,000 to 10,000 in the precipitation.

Synthesis of hydroxyfluorene-carboxilic acid and esters thereof
10351504 · 2019-07-16 ·

Methods of synthesizing phenanthrenequinone, 9-hydroxyfluorene-9-5 carboxylic acid (HFCA), methyl-9-hydroxyfluorene-carboxylate (HFCA methyl ester) and methyl-2-chloro-9-hydroxyfluorenecarboxylate, (Chlorflurenol) starting from preferred embodiment are disclosed. Several reaction products of phenanthrene are useful in industry, and are valuable plant growth regulators.

Systems And Methods For Producing Synthetic Hypericin

Improved systems and methods for producing synthetic hypericin at high volume and high purity.