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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, 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
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
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
Nandkishor Kotagale et al.
Pharmaceutical development and technology, 15(4), 431-437 (2010-03-20)
The present work deals with the formulation and evaluation of polymer-coated polysaccharide tablets of azathioprine prepared by direct compression method using different ratios of avicel (MCC), inulin and triacetin. The tablets formulations containing 25 mg of azathioprine were prepared and
J H Jeon et al.
Pharmaceutical development and technology, 13(6), 505-512 (2008-08-23)
The objective of these studies was to develop simple, implantable devices that intermittently release PTH(1-34) and thus could be used for locally stimulating bone formation. The formulations were based on the association polymer system of cellulose acetate phthalate and Pluronic
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