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Sodium salicylate - USP grade, high purity , CAS No.54-21-7

  • PharmPure™
  • USP
Item Number
S104179
Grouped product items
SKUSizeAvailabilityPrice Qty
S104179-250g
250g
In stock
$27.90

Cell-permeable anti-inflammatory agent

Basic Description

SynonymsSodium salicylate|54-21-7|Sodium 2-hydroxybenzoate|Enterosalicyl|Kerasalicyl|Salsonin|Alysine|Clin|Enterosalil|Entrosalyl|Glutosalyl|Kerosal|Magsalyl|Nadisal|Salisod|Aroall|Idocyl novum|Neo-salicyl|Benzoic acid, 2-hydroxy-, monosodium salt|Natrum salicyli
Specifications & PurityPharmPure™, USP
Biochemical and Physiological MechanismsSodium salicylate is a metabolite of acetylsalicylic acid, and functions by inhibiting NF κ B and reduces oxidative stress. The agent has the ability to protect against neurotoxicity induced by glutamate in rat studies. Along with aspirin , sodium salicyl
Shipped InNormal
GradePharmPure™, USP
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

An NF kappa B inhibitor and reducer of oxidative stress.

Associated Targets

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD(+)] 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name sodium;2-hydroxybenzoate
INCHI InChI=1S/C7H6O3.Na/c8-6-4-2-1-3-5(6)7(9)10;/h1-4,8H,(H,9,10);/q;+1/p-1
InChi Key ABBQHOQBGMUPJH-UHFFFAOYSA-M
Canonical SMILES C1=CC=C(C(=C1)C(=O)[O-])O.[Na+]
Isomeric SMILES C1=CC=C(C(=C1)C(=O)[O-])O.[Na+]
WGK Germany 1
RTECS VO5075000
PubChem CID 16760658
Molecular Weight 160.1
Beilstein 3732792

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

10 results found

Lot NumberCertificate TypeDateItem
J2310047Certificate of AnalysisOct 16, 2023 S104179
J2310048Certificate of AnalysisOct 16, 2023 S104179
B23171119Certificate of AnalysisFeb 23, 2023 S104179
B23171111Certificate of AnalysisFeb 22, 2023 S104179
A2331460Certificate of AnalysisFeb 06, 2023 S104179
K2215848Certificate of AnalysisNov 17, 2022 S104179
K2215847Certificate of AnalysisNov 16, 2022 S104179
A2219065Certificate of AnalysisJan 21, 2022 S104179
A2219060Certificate of AnalysisJan 20, 2022 S104179
F2230216Certificate of AnalysisJan 20, 2022 S104179

Chemical and Physical Properties

SolubilitySoluble in water (1000 g/l) at 20 °C, ethanol, and glycerol.
SensitivityLight sensitive.
Flash Point(°C)98.3 °C
Boil Point(°C)213 °C
Melt Point(°C)>300℃

Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS07
Signal Warning
Hazard Statements

H319:Causes serious eye irritation

H302:Harmful if swallowed

H361:Suspected of damaging fertility or the unborn child

Precautionary Statements

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P203:Obtain, read and follow all safety instructions before use.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P317:IF SWALLOWED: Get medical help.

P318:if exposed or concerned, get medical advice.

P337+P317:If eye irritation persists: Get medical help.

WGK Germany 1
RTECS VO5075000

Related Documents

References

1. Pritchard R et al..  (2018)  Celecoxib inhibits mitochondrial O2 consumption, promoting ROS dependent death of murine and human metastatic cancer cells via the apoptotic signalling pathway..  Biochem Pharmacol,  154  (318-334).  [PMID:29800556]

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