180963
Cellulose acetate butyrate
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About This Item
Productos recomendados
form
solid
Quality Level
extent of labeling
28.0-31.0 wt. % Acetyl
16.5-19.0 wt. % Butyryl
0.9-1.3 wt. % Hydroxyl
refractive index
n20/D 1.475 (lit.)
density
1.25 g/mL at 25 °C (lit.)
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Storage Class
11 - Combustible Solids
wgk_germany
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Los clientes también vieron
Decheng Ma et al.
Journal of pharmaceutical and biomedical analysis, 35(4), 779-788 (2004-06-15)
The purpose of this study was to qualitatively and quantitatively determine potential cellulose acetate butyrate (CAB) extractables in a way to meaningfully predict the in vivo exposure resulting from clinical administration. Extractions of CAB-381-20 were performed in several solvent systems
Jun Wuk Park et al.
Macromolecular bioscience, 5(9), 840-852 (2005-09-02)
Miscible blends of PHB and CAB were prepared by the solvent-casting method with various blend compositions, and their orientation behavior was investigated during uniaxial drawing. X-ray analysis revealed that the orientation of the crystallizable PHB component in the drawn PHB/CAB
Chen Huang et al.
Journal of biomedical materials research. Part A, 101(1), 115-122 (2012-07-25)
Cellulose acetate butyrate nanofibers were prepared separately by two electrospinning techniques; a needleless electrospinning using a disc as spinneret and a rotary drum as collector and a conventional needle electrospinning using a rotary drum as collector. Compared to the needle-electrospun
Soad A Yehia et al.
AAPS PharmSciTech, 10(1), 147-157 (2009-02-10)
The purpose of this study was to formulate budesonide (BUD) compression-coated tablets for colonic specific delivery. Pectin and guar gum were used as enzyme-dependent polymers. For comparison purposes, both pH- and time-dependent polymers were also tried. In vitro release studies
M Constantin et al.
International journal of pharmaceutics, 330(1-2), 129-137 (2006-10-10)
Poly(vinyl alcohol) (PVA) microspheres were prepared by dispersion reticulation with glutaraldehyde and further aminated. These microspheres were firstly loaded with diclofenac (DF) and then entrapped in cellulose acetate butyrate (CAB) microcapsules by an o/w solvent evaporation technique for intestinal delivery
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