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22192

Supelco

Cellulose Chromatography Resin

acetate phthalate

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About This Item

Formule empirique (notation de Hill):
C116H116O64
Numéro CAS:
9004-38-0
Poids moléculaire :
2534.12
Numéro MDL:
MFCD00072769
Code UNSPSC :
12000000
Nomenclature NACRES :
SB.52

product name

Cellulose acetate phthalate,

Forme

powder

Niveau de qualité

200

Technique(s)

LPLC: suitable

Matrice

acetylated cellulose

Groupe de la matrice active

phthalate

Capacité

1.0 meq/mL

Technique de séparation

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

Clé InChI

DMNFZTKVDDFCQE-WJXNTJCASA-N

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Catégories apparentées

Description générale

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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (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
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.
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
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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