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Merck
CN

P2008

Polyanetholesulfonic acid sodium salt

powder

Synonym(s):

Sodium polyanetholesulfonate

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About This Item

CAS Number:
55963-78-5
UNSPSC Code:
12162002
NACRES:
NA.77
MDL number:
MFCD00148427

Key Documents

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Product Name

Polyanetholesulfonic acid sodium salt, powder

color

yellow

InChI

1S/C10H12O.Na.H2O3S/c1-3-4-9-5-7-10(11-2)8-6-9;;1-4(2)3/h3-8H,1-2H3;;(H2,1,2,3)/q;+1;/p-2/b4-3+;;

SMILES string

C/C=C/C1=CC=C(C=C1)OC.[O-]S(=O)[O-].[Na+]

InChI key

JKJBFNAERWARKW-CZEFNJPISA-L

form

powder

storage condition

(Tightly closed. Dry.)

solubility

water: 1 g/10 mL, clear to hazy, yellow to very dark yellow-orange

Quality Level

200

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Application

Polyanetholesulfonic acid sodium salt:
  • has been used as a component in BACTEC plus aerobic/F medium or blood culture media to decrease the barrier for bacterial growth
  • has been used to inhibit the activity of classical pathway (CP) and alternative pathway (AP)
  • may be used in the preparation of bifunctional/polymeric composite gel beads to remove cationic dyes

Biochem/physiol Actions

Polyanetholesulfonic acid sodium salt is a polymeric phosphor. It can recognize ferric ion (Fe3+) effectively. Sodium polyanethole sulfonate (SPS) is used in commercial blood culture bottles as an anticoagulant. It can prevent the humoral and cellular elements that might interfere with the growth of bacteria. SPS may influence the complement system. It can block phagocytosis and leukocyte functions.

General description

Canonical SMILES: CC=CC1=CC=C(C=C1)OC.[O-]S(=O)[O-].[Na+]

Other Notes

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP0957
BCCN9750
BCCN8683
BCCN7560
BCCN7559

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Xiaojin Qin et al.
RSC advances, 8(54), 31231-31236 (2018-09-04)
Room-temperature phosphorescent materials have been a major focus of research and development during the past decades, due to their applications in OLEDs, photovoltaic cells, chemical sensors, and bioimaging. However, achieving polymeric phosphorescent materials without heavy-metal atoms and halogens under ambient
Ying Pei et al.
Antiviral research, 89(1), 98-108 (2010-11-27)
To investigate the anti-herpesvirus mechanism of pentagalloylglucose (PGG), we compared the proteomic changes between herpes simplex virus type 1 (HSV-1) infected MRC-5 cells with or without PGG-treatment, and between non-infected MRC-5 cells with or without PGG-treatment by 2-DE and MS-based
Ying Pei et al.
Biochemical and biophysical research communications, 405(2), 186-191 (2011-01-11)
Pentagalloylglucose (PGG) is a natural polyphenolic compound with broad-spectrum anti-viral activity, however, the mechanisms underlying anti-viral activity remain undefined. In this study, we investigated the effects of PGG on anti-viral activity against Herpes simplex virus type 1 (HSV-1) associated with
Damodar Gullipalli et al.
Journal of immunology (Baltimore, Md. : 1950), 210(10), 1543-1551 (2023-03-30)
Complement factor D (FD) is a rate-limiting enzyme of the alternative pathway (AP). Recent studies have suggested that it is synthesized as an inactive precursor and that its conversion to enzymatically active FD is catalyzed by mannan-binding lectin-associated serine protease
I Ginsburg et al.
Free radical biology & medicine, 7(4), 369-376 (1989-01-01)
Previous studies have demonstrated that a number of membrane-active agents are capable of binding to the surface of polymorphonuclear leukocytes (PMN) resulting in an augmentation of superoxide anion and hydrogen peroxide (H2O2) production in response to soluble stimuli. It is
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