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Merck
CN

62320

Sigma-Aldrich

(±)-α-Lipoic acid

≥98.0% (HPLC), solid

Synonym(s):

(±)-1,2-Dithiolane-3-pentanoic acid, 6,8-Dithiooctanoic acid, DL-α-Lipoic acid, DL-6,8-Thioctic acid, Lip(S2)

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1 G
CN¥178.03
10 G
CN¥1,582.03
50 G
CN¥4,543.02
250 G
CN¥14,521.69

CN¥178.03


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1 G
CN¥178.03
10 G
CN¥1,582.03
50 G
CN¥4,543.02
250 G
CN¥14,521.69

About This Item

Empirical Formula (Hill Notation):
C8H14O2S2
CAS Number:
Molecular Weight:
206.33
Beilstein:
81853
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

CN¥178.03


Please contact Customer Service for Availability

Request a Bulk Order

Product Name

(±)-α-Lipoic acid, ≥98.0%

Quality Level

Assay

≥98.0% (HPLC)
≥98.0%

form

solid

ign. residue

≤0.1%

loss

≤0.2% loss on drying

bp

>286 °C/1.013 hPa

mp

60-62 °C

solubility

water: 0.87 g/L at 22 °C

density

1.4 g/cm3 at 23 °C

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This Item
I8000I141P26600
Intralipid 20%, emulsion

I141

Intralipid

reaction suitability

reagent type: oxidant

reaction suitability

-

reaction suitability

-

reaction suitability

-

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

form

solid

form

powder

form

emulsion

form

powder

contains

stabilizer

contains

-

contains

-

contains

-

concentration

45 wt. % (IBX)

concentration

-

concentration

20%

concentration

-

General description

α-lipoic acid (ALA, thioctic acid) is a natural organosulfur compound produced in plants, animals and humans. It is a powerful antioxidant and plays a role in the forming nucleic acids, building blocks of DNA.[1]

This product is a racemic mixture.

Application

(±)-α-Lipoic acid has been used:

  • In in vitro lipoylation studies and in the pyruvate dehydrogenase complex (PDC)-pyruvate dehydrogenase kinase (PDHK) functional assay.[2]
  • To investigate its antioxidative effect on developing cerebellum of rats exposed to arsenic during postnatal period.[3]

Biochem/physiol Actions

(±)-α-Lipoic acid exhibits direct free radical scavenging property[4] and reduces the increased oxidative stress.[5] In addition, it might also exhibit prooxidant activity.[4] α-Lipoic acid functions as an important prosthetic group in α-keto acid dehydrogenase complexes of the mitochondria.[6] It acts as a potential therapeutic for diabetic patients with distal symmetric polyneuropathy (DSP).[5] α-Lipoic acid is also used in the treatment of energy-impaired and redox unbalanced diseases.[6]
Antioxidant and coenzyme needed for the activity of enzyme complexes such as pyruvate dehydrogenase and glycine decarboxylase.
Antioxidant and coenzyme needed for the activity of enzyme complexes such as those of pyruvate dehydrogenase and glycine decarboxylase. Exogenous thioctic acid is reduced intracellularly by two or more enzymes. The reduced form then influences a number of cell processes by direct radical scavenging, recycling of other antioxidants, increasing glutathione synthesis, and modulating transcription factor activity particularly that of NF-κB. Decreases the phagocytosis of myelin by macrophages.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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