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form
solid
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 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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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
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
Min Soo Park et al.
Langmuir : the ACS journal of surfaces and colloids, 22(10), 4594-4598 (2006-05-03)
We investigate the effects of interfacial energy between water and solvent as well as polymer concentration on the formation of porous structures of polymer films prepared by spin coating of cellulose acetate butyrate (CAB) in mixed solvent of tetrahydrofuran (THF)
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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