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Merck

191906

ヒドロキシプロピルセルロース

average Mw ~1,000,000, powder, 20 mesh particle size (99% through)

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この商品について

CAS番号:
UNSPSC Code:
12162002
NACRES:
NA.23
MDL number:
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SMILES string

N(C)(C)c1cc(c(cc1)C(N)CC)C

InChI

1S/C12H20N2/c1-5-12(13)11-7-6-10(14(3)4)8-9(11)2/h6-8,12H,5,13H2,1-4H3

InChI key

RRHXDYJWVYFMKV-UHFFFAOYSA-N

description

biological oxygen demand (BOD) 14,000 ppm

form

powder

autoignition temp.

752 °F

mol wt

average Mw ~1,000,000

impurities

<5 wt. %

particle size

20 mesh (99% through)

pH

5.0-8.5

interfacial tension mineral oil

12.5 dyn/cm, 0.1 wt. % in H2O (vs. mineral oil)

viscosity

1,275-3,500 cP, 1 wt. % in H2O(25 °C, Brookfield, spindle #3) (30 rpm)(lit.)

solubility

H2O: insoluble (above 45 °C), polar organic solvents: soluble

density

0.5 g/mL at 25 °C (lit.)

Quality Level

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Application

  • Thermo-responsive aqueous foams: Hydroxypropyl cellulose has been studied for its properties as a green polymer that can alter its solubility with temperature changes, making it suitable for responsive foam applications (Braunschweig, 2019).
  • Interaction mechanism in aqueous solutions: A study on the interaction between hydroxypropyl cellulose and water in solutions, focusing on the importance of polymer chain length in determining the physical properties of the solutions (Martin-Pastor and Stoyanov, 2020).
  • Corrosion inhibition: Hydroxypropyl cellulose has shown effectiveness as a corrosion inhibitor for aluminium in acidic environments, highlighting its potential in material science and engineering applications (Nwanonenyi et al., 2019).
  • Orally disintegrating films: This application involves the formulation design of hydroxypropyl cellulose films, aiming to enhance the delivery and dissolution profile of pharmaceuticals, making it significant in drug delivery and pharmaceutical sciences (Takeuchi et al., 2018).

保管分類

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

191906-100G: + 191906-BULK: + 191906-5G: + 191906-VAR: + 191906-250G:

jan


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Hyemin Choi et al.
Journal of pharmaceutical sciences, 101(8), 2941-2951 (2012-05-26)
Living organisms secrete minerals composed of peptides and proteins, resulting in "mesocrystals" of three-dimensional-assembled composite structures. Recently, this biomimetic polymer-directed crystallization technique has been widely applied to inorganic materials, although it has seldom been used with drugs. In this study
Ranjit M Dhenge et al.
International journal of pharmaceutics, 438(1-2), 20-32 (2012-09-11)
The present work focuses on the study of the progression of granules in different compartments along the length of screws in a twin screw granulator (TSG). The effects of varying powder feed rate; liquid to solid ratio and viscosity of
Maya Fujiwara et al.
Chemical & pharmaceutical bulletin, 60(11), 1380-1386 (2012-11-06)
We evaluated models for predicting spray mist diameter suitable for scaling-up the fluidized bed granulation process. By precise selection of experimental conditions, we were able to identify a suitable prediction model that considers changes in binder solution, nozzle dimension, and
Weibin Deng et al.
Drug development and industrial pharmacy, 39(2), 290-298 (2012-04-25)
The objective of this study was to improve the dissolution rate and to enhance the stability of a poorly water-soluble and low glass-trasition temperature (T(g)) model drug, fenofibrate, in low molecular weight grades of hydroxypropylcellulose matrices produced by hot-melt extrusion
Satomi Onoue et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 46(5), 492-499 (2012-04-14)
The present study was undertaken to develop a solid self-emulsifying drug delivery system of coenzyme Q(10) (CoQ(10)/s-SEDDS) with high photostability and oral bioavailability. The CoQ(10)/s-SEDDS was prepared by spray-drying an emulsion preconcentrate containing CoQ(10), medium-chain triglyceride, sucrose ester of fatty

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