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China Largest Manufacturer factory sales D-Mandelic Acid CAS 611-71-2
China Largest Manufacturer factory sales D-Mandelic Acid CAS 611-71-2
China Largest Manufacturer factory sales D-Mandelic Acid CAS 611-71-2
China Largest Manufacturer factory sales D-Mandelic Acid CAS 611-71-2
China Largest Manufacturer factory sales D-Mandelic Acid CAS 611-71-2

China Largest Manufacturer factory sales D-Mandelic Acid CAS 611-71-2

Min.Order / FOB Price:Get Latest Price

500 Kilogram

FOB Price:USD 1.0000 -2.0000

  • Min.Order :500 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

D-Mandelic Acid D-Mandelic Acid 611-71-2

Quick Details

  • Appearance:white powder
  • Application:Pharm chemicals industry
  • PackAge:25KG/Drum
  • ProductionCapacity:20|Metric Ton|Month
  • Storage:2-8°C
  • Transportation:By air /Sea/ coruier

Superiority:

                                PRODUCT DETAILS                           

Mandelic acid Basic information
Product Name: Mandelic acid
Synonyms: (R)-(-)-2-MANDELIC ACID;(R)-2-HYDROXY-2-PHENYLACETIC ACID;(R)-(-)-AMYGDALIC ACID;(R)-ALPHA-HYDROXYPHENYLACETIC ACID;R-(-)-ALPHA-HYDROXYPHENYLACETIC ACID;(R)-(-)-MANDELIC ACID;(R)-MANDELIC ACID;D-ALPHA-HYDROXYPHENYLACETIC ACID
CAS: 611-71-2
MF: C8H8O3
MW: 152.15
EINECS: 210-276-6
Product Categories: Aromatics;Chiral Reagents;Chiral Compounds;Miscellaneous;Intermediates & Fine Chemicals;Pharmaceuticals;chiral;Analytical Chemistry;Carboxylic Acids (Chiral);Chiral Building Blocks;e.e. / Absolute Configuration Determination (NMR);Enantiomer Excess & Absolute Configuration Determination;for Resolution of Bases;Optical Resolution;FINE Chemical & INTERMEDIATES;Synthetic Organic Chemistry;Chiral Compound;Cosmetic
Mol File: 611-71-2.mol
Mandelic acid Structure
 
Mandelic acid Chemical Properties
Melting point  131-133 °C(lit.)
alpha  -150 º (c=2.5, H2O)
Boiling point  214.6°C (rough estimate)
density  1.1677 (rough estimate)
refractive index  -153.5 ° (C=1, H2O)
Fp  >190℃
storage temp.  Store below +30°C.
solubility  109.8g/l soluble
pka 3.37(at 25℃)
form  Crystalline Powder, Crystals or Flakes
color  White to slightly yellow-beige
PH 3.34(1 mM solution);2.75(10 mM solution);2.22(100 mM solution);
optical activity [α]25/D 151°, c = 1 in ethanol
Water Solubility  It is partly soluble in water, freely soluble in isopropyl and ethyl alcohol.
Sensitive  Light Sensitive
BRN  2691094
Stability: Stable, but light sensitive. Combustible. Incompatible with strong bases, strong oxidizing agents.
InChIKey IWYDHOAUDWTVEP-SSDOTTSWSA-N
CAS DataBase Reference 611-71-2(CAS DataBase Reference)
EPA Substance Registry System Benzeneacetic acid, .alpha.-hydroxy-, (.alpha.R)- (611-71-2)
 
Safety Information
Hazard Codes  Xi
Risk Statements  41-36/37/38
Safety Statements  22-24/25-36-26-39-37/39
WGK Germany  1
Hazard Note  Irritant/Light Sensitive
TSCA  Yes
HS Code  29181980
Toxicity LD50 orally in Rabbit: 5000 mg/kg
MSDS Information
Provider Language
2-Phenylglycolic acid English
SigmaAldrich English
ACROS English
ALFA English
 
Mandelic acid Usage And Synthesis
Chemical Properties white to light yellow crystal powde
Uses Antiseptic (urinary).
Uses (R)-(-)-Mandelic acid, is used as a antiseptic ingredient particularly against urinary tract infections.Mandelic acid and its derivatives are used to apply the dual activities as an antibacterial agent and as an antiaging agent. It is used as an intermediate for the synthesis of target molecules for other applications.
Uses (R)-( )-Mandelic acid can be used:
  • As a chiral acid in the separation of diastereomeric salts for the synthesis of chiral pyridoindole based building block.
  • In the study of chiral acid selectivity of poly(3,4-ethylenedioxythiophene) (PEDOT) based chiral conducting polymers.
Synthesis Reference(s) The Journal of Organic Chemistry, 33, p. 2565, 1968 DOI: 10.1021/jo01270a105
Synthetic Communications, 18, p. 2141, 1988 DOI: 10.1080/00397918808068285
General Description

(R)-(-)-Mandelic acid, a chiral resolving agent, is also used as a building block to synthesize pharmaceutical drugs such as penicillin and cephalosporin. It can be synthesized from (R,S)-mandelonitrile with high yield and enantioselectivity using nitrilase enzyme.

Purification Methods Purify the mandelic acids by recrystallisation from H2O, *C6H6 or CHCl3. [Roger J Chem Soc 2168 1932,Jamison & Turner J Chem Soc 611 1942.] They have solubilities in H2O of ca 11% at 25o. [Banks & Davies J Chem Soc 73 1938.] The S-benzylisothiuronium salts has m 180o (from H2O) and [] D 25 (+) and (-) 57o (c20, EtOH) [El Masri et al. Biochem J 68 199 1958]. [Beilstein 10 IV 564.]
 
Mandelic acid Preparation Products And Raw materials
Raw materials (S)-(+)-O-Acetyl-L-mandelic acid-->Vinyl acetate
Preparation Products 1H-Azepine-4-carboxylicacid,hexahydro-,methylester,(4R)-(9CI)


                                                                       Group profiles


Leader Biochemical Group is a large leader incorporated industry manufacturers and suppliers of advanced refined raw materials From the year of 1996 when our factory was put into production to year of 2020, our group has successively invested in more than 52 factories with shares and subordinates.We focus on manufacture Pharm & chemicals, functional active ingredients, nutritional Ingredients, health care products, cosmetics, pharmaceutical and refined feed, oil, natural plant ingredients industries to provide top quality of GMP standards products.All the invested factories' product lines cover API and intermediates, vitamins, amino acids, plant extracts, daily chemical products, cosmetics raw materials, nutrition and health care products, food additives, feed additives, essential oil products, fine chemical products and agricultural chemical raw materials And flavors and fragrances. Especially in the field of vitamins, amino acids, pharmaceutical raw materials and cosmetic raw materials, we have more than 20 years of production and sales experience. All products meet the requirements of high international export standards and have been recognized by customers all over the world. Our manufacture basement & R&D center located in National Aerospace Economic & Technical Development Zone Xi`an Shaanxi China. Now not only relying on self-cultivation and development as well as maintains good cooperative relations with many famous research institutes and universities in China. Now, we have closely cooperation with Shanghai Institute of Organic Chemistry of Chinese Academy of Science, Beijing Institute of Material Medical of Chinese Academy of Medical Science, China Pharmaceutical University, Zhejiang University. Closely cooperation with them not only integrating Science and technology resources, but also increasing the R&D speed and improving our R&D power. Offering Powerful Tech supporting Platform for group development. Keep serve the manufacture and the market as the R&D central task, focus on the technical research.  Now there are 3 technology R & D platforms including biological extract, microorganism fermentation and chemical synthesis, and can independently research and develop kinds of difficult APIs and pharmaceutical intermediates. With the strong support of China State Institute of Pharmaceutical Industry (hereinafter short for CSIPI), earlier known as Shanghai Institute of Pharmaceutical Industry (SIPI), we have unique advantages in the R & D and industrialization of high-grade, precision and advanced products.  Now our Group technical force is abundant, existing staff more that 1000 people, senior professional and technical staff accounted for more than 50% of the total number of employees, including 15 PhD research and development personnel, 5 master′ S degree in technical and management personnel 9 people. We have advanced equipment like fermentation equipment and technology also extraction, isolation, purification, synthesis with rich production experience and strict quality control system, According to the GMP required, quickly transforming the R&D results to industrial production in time, it is our advantages and our products are exported to North and South America, Europe, Middle East, Africa, and other five continents and scale the forefront in the nation, won good international reputation.  We believe only good quality can bring good cooperation, quality is our key spirit during our production, we are warmly welcome clients and partner from all over the world contact us for everlasting cooperation, Leader will be your strong, sincere and reliable partner in China.

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Details:

                                                       Product information

Mandelic acid Basic information
Product Name: Mandelic acid
Synonyms: (R)-(-)-2-MANDELIC ACID;(R)-2-HYDROXY-2-PHENYLACETIC ACID;(R)-(-)-AMYGDALIC ACID;(R)-ALPHA-HYDROXYPHENYLACETIC ACID;R-(-)-ALPHA-HYDROXYPHENYLACETIC ACID;(R)-(-)-MANDELIC ACID;(R)-MANDELIC ACID;D-ALPHA-HYDROXYPHENYLACETIC ACID
CAS: 611-71-2
MF: C8H8O3
MW: 152.15
EINECS: 210-276-6
Product Categories: Aromatics;Chiral Reagents;Chiral Compounds;Miscellaneous;Intermediates & Fine Chemicals;Pharmaceuticals;chiral;Analytical Chemistry;Carboxylic Acids (Chiral);Chiral Building Blocks;e.e. / Absolute Configuration Determination (NMR);Enantiomer Excess & Absolute Configuration Determination;for Resolution of Bases;Optical Resolution;FINE Chemical & INTERMEDIATES;Synthetic Organic Chemistry;Chiral Compound;Cosmetic
Mol File: 611-71-2.mol
Mandelic acid Structure
 
Mandelic acid Chemical Properties
Melting point  131-133 °C(lit.)
alpha  -150 º (c=2.5, H2O)
Boiling point  214.6°C (rough estimate)
density  1.1677 (rough estimate)
refractive index  -153.5 ° (C=1, H2O)
Fp  >190℃
storage temp.  Store below +30°C.
solubility  109.8g/l soluble
pka 3.37(at 25℃)
form  Crystalline Powder, Crystals or Flakes
color  White to slightly yellow-beige
PH 3.34(1 mM solution);2.75(10 mM solution);2.22(100 mM solution);
optical activity [α]25/D 151°, c = 1 in ethanol
Water Solubility  It is partly soluble in water, freely soluble in isopropyl and ethyl alcohol.
Sensitive  Light Sensitive
BRN  2691094
Stability: Stable, but light sensitive. Combustible. Incompatible with strong bases, strong oxidizing agents.
InChIKey IWYDHOAUDWTVEP-SSDOTTSWSA-N
CAS DataBase Reference 611-71-2(CAS DataBase Reference)
EPA Substance Registry System Benzeneacetic acid, .alpha.-hydroxy-, (.alpha.R)- (611-71-2)
 
Safety Information
Hazard Codes  Xi
Risk Statements  41-36/37/38
Safety Statements  22-24/25-36-26-39-37/39
WGK Germany  1
Hazard Note  Irritant/Light Sensitive
TSCA  Yes
HS Code  29181980
Toxicity LD50 orally in Rabbit: 5000 mg/kg
MSDS Information
Provider Language
2-Phenylglycolic acid English
SigmaAldrich English
ACROS English
ALFA English
 
Mandelic acid Usage And Synthesis
Chemical Properties white to light yellow crystal powde
Uses Antiseptic (urinary).
Uses (R)-(-)-Mandelic acid, is used as a antiseptic ingredient particularly against urinary tract infections.Mandelic acid and its derivatives are used to apply the dual activities as an antibacterial agent and as an antiaging agent. It is used as an intermediate for the synthesis of target molecules for other applications.
Uses (R)-( )-Mandelic acid can be used:
  • As a chiral acid in the separation of diastereomeric salts for the synthesis of chiral pyridoindole based building block.
  • In the study of chiral acid selectivity of poly(3,4-ethylenedioxythiophene) (PEDOT) based chiral conducting polymers.
Synthesis Reference(s) The Journal of Organic Chemistry, 33, p. 2565, 1968 DOI: 10.1021/jo01270a105
Synthetic Communications, 18, p. 2141, 1988 DOI: 10.1080/00397918808068285
General Description

(R)-(-)-Mandelic acid, a chiral resolving agent, is also used as a building block to synthesize pharmaceutical drugs such as penicillin and cephalosporin. It can be synthesized from (R,S)-mandelonitrile with high yield and enantioselectivity using nitrilase enzyme.

Purification Methods Purify the mandelic acids by recrystallisation from H2O, *C6H6 or CHCl3. [Roger J Chem Soc 2168 1932,Jamison & Turner J Chem Soc 611 1942.] They have solubilities in H2O of ca 11% at 25o. [Banks & Davies J Chem Soc 73 1938.] The S-benzylisothiuronium salts has m 180o (from H2O) and [] D 25 (+) and (-) 57o (c20, EtOH) [El Masri et al. Biochem J 68 199 1958]. [Beilstein 10 IV 564.]
 
Mandelic acid Preparation Products And Raw materials
Raw materials (S)-(+)-O-Acetyl-L-mandelic acid-->Vinyl acetate
Preparation Products 1H-Azepine-4-carboxylicacid,hexahydro-,methylester,(4R)-(9CI)

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