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Merck
CN

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:
23151817
NACRES:
SB.52

Key Documents

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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

SMILES string

O1[C@H]([C@@H]([C@H]([C@@H]([C@H]1COC(=O)C)O)OC(=O)c4c(cccc4)C(=O)O)O)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)OC(=O)c3c(cccc3)C(=O)O)O)COC(=O)C

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

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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
D Quintanar-Guerrero et al.
International journal of pharmaceutics, 188(2), 155-164 (1999-10-16)
Pseudolatexes were obtained by a new process based on an emulsification-diffusion technique involving partially water-miscible solvents. The preparation method consisted of emulsifying an organic solution of polymer (saturated with water) in an aqueous solution of a stabilizing agent (saturated with
Praful Balavant Deshpande et al.
Pharmaceutical development and technology, 15(4), 369-378 (2009-09-24)
The aim of the present study was to formulate and evaluate controlled release polymeric ocular delivery of acyclovir. Reservoir-type ocular inserts were fabricated by sandwiching hydroxypropyl methylcellulose (HPMC) matrix film containing acyclovir between two rate controlling membranes of cellulose acetate
Samantha Pillay et al.
International journal of pharmaceutics, 382(1-2), 277-290 (2009-08-26)
This study focused on the design, biometric simulation and optimization of an intracranial nano-enabled scaffold device (NESD) for the site-specific delivery of dopamine (DA) as a strategy to minimize the peripheral side-effects of conventional forms of Parkinson's disease therapy. The
J R McClanahan et al.
International journal of antimicrobial agents, 38(6), 530-533 (2011-09-17)
WLBU2 is a peptide antibiotic designed for broad antimicrobial activity, including bacteria associated with periodontal disease. Although periodontitis is associated with various systemic conditions, ranging from cardiovascular disease to preterm birth, local therapy is needed to treat the source of
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