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Merck

22192

Supelco

Cellulose Chromatography Resin

acetate phthalate

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About This Item

Empirische Formel (Hill-System):
C116H116O64
CAS-Nummer:
Molekulargewicht:
2534.12
MDL-Nummer:
UNSPSC-Code:
12000000
NACRES:
SB.52

Produktbezeichnung

Cellulose-acetatphthalat,

Form

powder

Qualitätsniveau

Methode(n)

LPLC: suitable

Matrix

acetylated cellulose

Aktive Matrixgruppe

phthalate

Kapazität

1.0 meq/mL

Trenntechnik

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

InChIKey

DMNFZTKVDDFCQE-WJXNTJCASA-N

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Allgemeine Beschreibung

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.

Anwendung

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Kunden haben sich ebenfalls angesehen

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
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
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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