Recommended Products
form
powder
mol wt
average Mn ~70,000
extent of labeling
12-15 wt. % Acetyl
35-39 wt. % Butyryl
1.2-2.2 wt. % Hydroxyl
refractive index
n20/D 1.475 (lit.)
density
1.25 g/mL at 25 °C (lit.)
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Storage Class Code
11 - Combustible Solids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Customers Also Viewed
W M Obeidat et al.
Journal of microencapsulation, 21(1), 47-57 (2004-01-14)
Theophylline microspheres were prepared by the emulsion-solvent evaporation method using cellulose acetate butyrate (CAB381-20) and mixtures of CAB381-20(R) and cellulose acetate phthalate. The physical state of the drug, polymers and microspheres surfaces were determined using scanning electron microscopy. For those
Gheorghe Fundueanu et al.
Biomaterials, 26(20), 4337-4347 (2005-02-03)
Sulfopropylated dextran microspheres (SP-Ms), (Dm = 80 microm) loaded with a water soluble drug (Tetracycline HCl), were included in cellulose acetate butyrate (CAB) microcapsules. Spherical CAB microcapsules were obtained by oil in water (o/w) solvent evaporation method in the presence
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
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
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