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71943

Sigma-Aldrich

Sodium salicylate

tested according to Ph. Eur.

Sinonimo/i:

Natrii salicylas, 2-Hydroxybenzoic acid sodium salt, Salicylic acid sodium salt, Sodium 2-hydroxybenzoate

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About This Item

Formula condensata:
HOC6H4COONa
Numero CAS:
54-21-7
Peso molecolare:
160.10
Beilstein:
3732792
Numero CE:
200-198-0
Numero MDL:
MFCD00002440
Codice UNSPSC:
12352201
ID PubChem:
329763648
NACRES:
NA.21

agenzia

USP/NF
tested according to Ph. Eur.

Livello qualitativo

100

Forma fisica

crystals

Colore

white

Intervallo di pH utile

6.85 (26.3 °C)

Punto di fusione

>300 °C (lit.)

Solubilità

water: 575.7 g/L at 25 °C (77 °F)

applicazioni

pharmaceutical (small molecule)

Stringa SMILE

[Na+].Oc1ccccc1C([O-])=O

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
ABBQHOQBGMUPJH-UHFFFAOYSA-M

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Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H319,H361d

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

208.9 °F - Pensky-Martens closed cup

Punto d’infiammabilità (°C)

98.3 °C - Pensky-Martens closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCJ7211
BCCG9418
BCCG2202
BCCD4378
BCCD1203

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Kui Wang et al.
Journal of medicinal chemistry, 52(20), 6402-6412 (2009-10-16)
Viologens are showing an increasing number of scientific and technical applications in addition to their use as herbicides. However, their high toxicity poses considerable risks to human health, society, and the environment. In this context, we propose a new therapeutic
Yanguang Cao et al.
The Journal of pharmacology and experimental therapeutics, 339(3), 896-904 (2011-09-10)
Type 2 diabetes mellitus (T2DM) arises owing to insulin resistance and β-cell dysfunction. Chronic inflammation is widely identified as a cause of T2DM. The Goto-Kakizaki (GK) rat is a spontaneous rodent model for T2DM with chronic inflammation. The purpose of
Rainer Amann et al.
European journal of pharmacology, 447(1), 1-9 (2002-07-11)
Aspirin (acetylsalicylic acid) is one of the most widely used drugs worldwide. It acetylates cyclooxygenases thereby irreversibly blocking the conversion of arachidonic acid to prostanoids. Biotransformation of aspirin yields salicylate, a compound that possesses similar anti-inflammatory potency as aspirin but
Astam K Patra et al.
Journal of hazardous materials, 201-202, 170-177 (2011-12-16)
We report a highly efficient synthetic strategy for self-assembled mesoporous γ-Al(2)O(3) materials using sodium salicylate as template. The mesoporous γ-Al(2)O(3) samples synthesized following this strategy have high surface areas (231-497 m(2)g(-1)), consist of crystalline tiny spherical nanoparticles of dimensions ca.
Yan-Yan Su et al.
PloS one, 7(10), e46969-e46969 (2012-10-17)
Sodium salicylate (NaSal), an aspirin metabolite, can cause tinnitus in animals and human subjects. To explore neural mechanisms underlying salicylate-induced tinnitus, we examined effects of NaSal on neural activities of the medial geniculate body (MGB), an auditory thalamic nucleus that
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