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22192

Supelco

Cellulose Chromatography Resin

acetate phthalate

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About This Item

Empirical Formula (Hill Notation):
C116H116O64
CAS Number:
9004-38-0
Molecular Weight:
2534.12
MDL number:
MFCD00072769
UNSPSC Code:
12000000
NACRES:
SB.52

product name

Cellulose acetate phthalate,

form

powder

Quality Level

200

technique(s)

LPLC: suitable

matrix

acetylated cellulose

matrix active group

phthalate

capacity

1.0 meq/mL

separation technique

reversed phase

InChI

1S/C32H34O19/c1-13(33)45-11-19-21(35)25(49-29(42)17-9-5-3-7-15(17)27(38)39)23(37)32(48-19)51-24-20(12-46-14(2)34)47-31(44)26(22(24)36)50-30(43)18-10-6-4-8-16(18)28(40)41/h3-10,19-26,31-32,35-37,44H,11-12H2,1-2H3,(H,38,39)(H,40,41)/t19-,20-,21-,22+,23-,24-,25+,26-,31-,32+/m1/s1

InChI key

DMNFZTKVDDFCQE-WJXNTJCASA-N

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General description

Cellulose acetate phthalate (CAP) is a microbicide which inactivates sexually transmitted disease (STD) pathogens like HIV-1. CAP has been used for enteric film coating of tablets and capsules.

Application

CAP is used as a stabiling agent in the preparation of Pseudolatex.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL3210
BCCH4232
BCCD4766
BCBW5667
BCBN9248V

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A Robert Neurath et al.
BMC infectious diseases, 3, 27-27 (2003-11-18)
Cellulose acetate phthalate (CAP) has been used for several decades in the pharmaceutical industry for enteric film coating of oral tablets and capsules. Micronized CAP, available commercially as "Aquateric" and containing additional ingredients required for micronization, used for tablet coating
A Robert Neurath et al.
BMC infectious diseases, 2, 6-6 (2002-05-02)
Cellulose acetate phthalate (CAP), a promising candidate microbicide for prevention of sexual transmission of the human immunodeficiency virus type 1 (HIV-1) and other sexually transmitted disease (STD) pathogens, was shown to inactivate HIV-1 and to block the coreceptor binding site
Azita Haddadi et al.
Journal of microencapsulation, 23(6), 698-712 (2006-11-23)
This work describes the formulation and characterization of urea-loaded microspheres prepared using various polymers such as ethyl cellulose (EC), cellulose acetate phthalate (CAP) and poly (D,L-lactic-co-glycolic acid) (PLGA), along with the utilization of a solvent evaporation technique. The effect of
Chaobo Huang et al.
Biomaterials, 33(3), 962-969 (2011-10-25)
Despite many advances in modern medicine, human immunodeficiency virus (HIV) still affects the health of millions of people world-wide and much effort is put in developing methods to either prevent infection or to eradicate the virus after infection has occurred.
Ju Hyeong Jeon et al.
Journal of periodontology, 79(8), 1457-1464 (2008-08-05)
The cholesterol-lowering drug simvastatin promotes bone formation in cell cultures and animal models. In previous studies, devices for the controlled, localized delivery of simvastatin hydroxyacid enhanced osteoblastic activity in vitro. The objective of this investigation was to determine bioactivity of
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