1200-22-2

  • Product Name:R-(+)-Lipoic acid
  • Molecular Formula:C8H14O2S2
  • Purity:99%
  • Molecular Weight:206.33
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Product Details;

CasNo: 1200-22-2

Molecular Formula: C8H14O2S2

Appearance: yellow crystalline solid

Hot Sale Factory Supply High Purity R-(+)-Lipoic acid 1200-22-2 Safe Transportation

  • Molecular Formula:C8H14O2S2
  • Molecular Weight:206.33
  • Appearance/Colour:yellow crystalline solid 
  • Melting Point:48-52 °C(lit.) 
  • Refractive Index:114 ° (C=1, EtOH) 
  • Boiling Point:362.5 °C at 760 mmHg 
  • PKA:5.4(at 25℃) 
  • Flash Point:173 °C 
  • PSA:87.90000 
  • Density:1.218 g/cm3 
  • LogP:2.78510 

(R)-(+)-1,2-Dithiolane-3-pentanoic acid(Cas 1200-22-2) Usage

Chemical Properties

Yellow Crystalline Solid

Uses

A fat-metabolism stimulator

General Description

α-Lipoic acid is an antioxidant which is generally present in plants, animals and many other microorganisms.

Biochem/physiol Actions

(R)-(+)-α-Lipoic acid was shown to significantly increase pyruvate oxidation while abrogating fatty acid oxidation in rat hepatocytes. These effects make R-(+)-α-Lipoic acid a promising treatment option for the treatment of Type II diabetes. It is a biological antioxidant with prooxidant activities, its therapeutic potential is widely investigated, e.g. in the treatment for Alzheimer′s disease.

InChI:InChI=1/C8H14O2S2/c9-8(10)4-2-1-3-7-5-6-11-12-7/h7H,1-6H2,(H,9,10)/t7-/m1/s1

1200-22-2 Relevant articles

Enantioselective Synthesis of R-(+)-α-Lipoic Acid

Page, Philip C. Bulman,Rayner, Christopher M.,Sutherland, Ian O.

, p. 1408 - 1409 (1986)

The title compound has been synthesised ...

ASYMMETRIC SYNTHESIS VIA ACETAL TEMPLATES. 12. HIGHLY DIASTEREOSELECTIVE COUPLING REACTIONS WITH A KETENE ACETAL. AN EFFICIENT, ASYMMETRIC SYNTHESIS OF R-(+)-α-LIPOIC ACID.

Elliott, John D.,Steele, John,Johnson, William S.

, p. 2535 - 2538 (1985)

TiCl4 catalyzes the essentially quantita...

Coevolution of the Activity and Thermostability of an ?-Keto Ester Reductase for Better Synthesis of an (R)-α-Lipoic Acid Precursor

Chen, Qi,Xu, Jian-He,Xu, Yao,Zhang, Zhi-Jun,Zheng, Gao-Wei

, (2019)

In this work, we have identified a signi...

Stereocontrolled reactions induced by a thermolabile group. Synthesis of optically active 1,3-diols

Bloch, Robert,Bortolussi, Michel,Girard, Christian,Seck, Matar

, p. 453 - 462 (1992)

Wittig Horner-Michael reactions of phosp...

Microwave-assisted resolution of α-lipoic acid catalyzed by an ionic liquid co-lyophilized lipase

Liu, Ning,Wang, Lei,Wang, Zhi,Jiang, Liyan,Wu, Zhuofu,Yue, Hong,Xie, Xiaona

, p. 9949 - 9960 (2015)

The combination of the ionic liquid co-l...

Preparation method of R-lipoic acid

-

Paragraph 0039; 0065-0067; 0085-0087; 0105-0106, (2021/07/31)

The invention discloses a preparation me...

Synthesis method R -lipoic acid

-

Paragraph 0042; 0070-0074; 0094-0096; 0116-0117, (2021/09/26)

A synthesis method of R -lipoic acid com...

Preparation method of R-lipoic acid tromethamine salt

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Paragraph 0028; 0036; 0038; 0045; 0047; 0054, (2021/05/12)

The invention relates to a preparation m...

Preparation method of D-lipoic acid

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Paragraph 0040-0070, (2021/02/24)

The invention relates to a preparation m...

1200-22-2 Process route

(7R,10S)-7-Isopropyl-10-methyl-1,5-dithia-spiro[5.5]undecane
114529-48-5

(7R,10S)-7-Isopropyl-10-methyl-1,5-dithia-spiro[5.5]undecane

l-menthone
3391-87-5,17627-49-5,7786-64-3

l-menthone

(R)-1,2-dithiolane-3-pentanoic acid
1200-22-2

(R)-1,2-dithiolane-3-pentanoic acid

Conditions
Conditions Yield
Multistep reaction;
 
[ethyl (5R)-5-(1,2-dithiolan-3yl)pentanoate]
104726-74-1

[ethyl (5R)-5-(1,2-dithiolan-3yl)pentanoate]

(R)-1,2-dithiolane-3-pentanoic acid
1200-22-2

(R)-1,2-dithiolane-3-pentanoic acid

Conditions
Conditions Yield
With ethanol; water; sodium hydroxide; at 50 ℃; for 2h; Reagent/catalyst; Temperature;
96.1%
With sodium hydroxide; In ethanol; water; at 50 ℃; for 2h; Solvent; Temperature;
96%
With water; sodium hydroxide; In methanol; at 48 ℃; for 130h; Temperature; Solvent;
94%
With hydrogenchloride; potassium hydroxide; In ethanol; for 24h; Ambient temperature;
75%
With potassium hydroxide; In ethanol; at 20 ℃; for 24h;
75%
With potassium hydroxide; In ethanol; at 20 ℃; for 24h;
75%
hydrolysis;
 
With sodium hydroxide;
 

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