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Sodium thioctate

Name: Sodium thioctate
Brand: 2A Biotech
SKU: 2A-9028313

CAS Number2319-84-8

SynonymsEpakon; Sodium thioctate; Tioctene; Eparidasi; Thioctan; Tioctan; Tioicorzan; Tioctinessa; 6,8-Thioctic acid sodium salt; Thioctic acid sodium salt

Molecular FormulaC8H13NaO2S2

Molecular Weight228.30700

Purity98.00%

Boiling Point362.5ºC at 760mmHg

Melting Point241-253 °C

MSDSChinese English

Cat. No.: 2A-9028313 Purity: 98.00%

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Quality Control of [ 2319-84-8 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number	2319-84-8
Catalog No.	2A-9028313
Chinese Name	硫辛酸钠
Synonyms	Epakon; Sodium thioctate; Tioctene; Eparidasi; Thioctan; Tioctan; Tioicorzan; Tioctinessa; 6,8-Thioctic acid sodium salt; Thioctic acid sodium salt
Molecular Formula	C8H13NaO2S2
Molecular Weight	228.30700
Purity	98.00
Boiling Point	362.5ºC at 760mmHg
Melting Point	241-253 °C
Storage Condition	room temperature
Application	Sodium alpha-lipoate (sodium lipoate; (±)-sodium alpha-lipoate; DL-sodium alpha-lipoate) is an antioxidant. Sodium alpha-lipoate inhibits NF-κB-dependent HIV-1 LTR activation. Sodium alpha-lipoate ind
HTC	2934999090
PubChem ID	14773759
SMILES	O=C([O-])CCCCC1CCSS1.[Na+]
InChI	InChI=1S/C8H14O2S2.Na/c9-8(10)4-2-1-3-7-5-6-11-12-7;/h7H,1-6H2,(H,9,10);/q;+1/p-1
InChI Key	UUDFBRWLHZIIQX-UHFFFAOYSA-M
Bioactivity	α-Lipoic Acid sodium (Thioctic acid sodium; (±)-α-Lipoic acid sodium; DL-α-Lipoic acid sodium) is an antioxidant. α-Lipoic Acid sodium inhibits NF-κB-dependent HIV-1 LTR activation. α-Lipoic Acid sodium induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells. α-Lipoic Acid sodium can be used for researching diabetes, neuropathy, obesity, abnormal pregnancy and other diseases[1][2][3][4][5]. Related Catalog Signaling Pathways >> Apoptosis >> Apoptosis Research Areas >> Cancer Signaling Pathways >> Anti-infection >> HIV Research Areas >> Endocrinology Research Areas >> Infection Research Areas >> Metabolic Disease Research Areas >> Neurological Disease Target NF-κB HIV Human Endogenous Metabolite Microbial Metabolite References [1]. Xiao L, et al. Activity of the dietary antioxidant ergothioneine in a virus gene-based assay for inhibitors of HIV transcription. Biofactors. 2006;27(1-4):157-65. [2]. Lei D, et al. Synergistic neuroprotective effect of rasagiline and idebenone against retinal ischemia-reperfusion injury via the Lin28-let-7-Dicer pathway. Oncotarget. 2018 Jan 30;9(15):12137-12153. [3]. Yang Y, et al. Alpha-lipoic acid improves high-fat diet-induced hepatic steatosis by modulating the transcription factors SREBP-1, FoxO1 and Nrf2 via the SIRT1/LKB1/AMPK pathway. J Nutr Biochem. 2014 Nov;25(11):1207-1217. [4]. Pibiri M, et al. α-Lipoic acid induces Endoplasmic Reticulum stress-mediated apoptosis in hepatoma cells. Sci Rep. 2020 Apr 28;10(1):7139. [5]. Salehi B, et al. Insights on the Use of α-Lipoic Acid for Therapeutic Purposes. Biomolecules. 2019 Aug 9;9(8):356. Chemical & Physical Properties Boiling Point 362.5ºC at 760mmHg Melting Point 241-253 °C Molecular Formula C8H13NaO2S2 Molecular Weight 228.30700 Flash Point 173ºC Exact Mass 228.02500 PSA 90.73000 LogP 1.45040 Vapour Pressure 3.07E-06mmHg at 25°C InChIKey UUDFBRWLHZIIQX-UHFFFAOYSA-M SMILES O=C([O-])CCCCC1CCSS1.[Na+]
Use of	Properties Name sodium,5-(dithiolan-3-yl)pentanoate Synonym More Synonyms Sodium thioctate Biological Activity Related Catalog Signaling Pathways >> Apoptosis >> Apoptosis Research Areas >> Cancer Signaling Pathways >> Anti-infection >> HIV Research Areas >> Endocrinology Research Areas >> Infection Research Areas >> Metabolic Disease Research Areas >> Neurological Disease Human Endogenous Metabolite Microbial Metabolite References [1]. Xiao L, et al. Activity of the dietary antioxidant ergothioneine in a virus gene-based assay for inhibitors of HIV transcription. Biofactors. 2006;27(1-4):157-65. [2]. Lei D, et al. Synergistic neuroprotective effect of rasagiline and idebenone against retinal ischemia-reperfusion injury via the Lin28-let-7-Dicer pathway. Oncotarget. 2018 Jan 30;9(15):12137-12153. [4]. Pibiri M, et al. α-Lipoic acid induces Endoplasmic Reticulum stress-mediated apoptosis in hepatoma cells. Sci Rep. 2020 Apr 28;10(1):7139. [5]. Salehi B, et al. Insights on the Use of α-Lipoic Acid for Therapeutic Purposes. Biomolecules. 2019 Aug 9;9(8):356. Chemical & Physical Properties Molecular Formula C8H13NaO2S2 Exact Mass 228.02500 PSA 90.73000 LogP 1.45040 InChIKey UUDFBRWLHZIIQX-UHFFFAOYSA-M
Tax Rebate	13.0%
Supervision	None. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport Info	Product name: Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Sodium thioctate

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