D(-)Mandelic Acid CAS NO.611-71-2

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D(-)Mandelic Acid CAS NO.611-71-2
Details
MF: C8H8O3
MW:152.15
EINECS:210-276-6
Category
Other Intermediates
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Description

D(-)Mandelic acid Basic information

Referrence

Product Name:D(-)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

D(-)Mandelic acid Chemical Properties

Melting point131-133 °C(lit.)
Boiling point214.6°C (rough estimate)
Density1.1677 (rough estimate)
Refractive index-153.5 ° (C=1, H2O)

Specific rotation

-150 º (c=2.5, H2O)
Flash point>190℃
Storage conditionsStore below +30°C.
Solubility109.8g/l soluble
Coefficient of acidity (pKa)3.37(at 25℃)
FormCrystalline Powder, Crystals or Flakes
ColorWhite to slightly yellow-beige
PH3.34(1 mM solution);2.75(10 mM solution);2.22(100 mM solution)
Optical rotation[α]25/D 151°, c = 1 in ethanol
Water solubilityIt is partly soluble in water, freely soluble in isopropyl and ethyl alcohol.
SensitivityLight Sensitive
BRN 2691094
StabilityStable, but light sensitive. Combustible. Incompatible with strong bases, strong oxidizing agents.

D(-)Mandelic acid Usage And Synthesis

Biological activityD-(-)-Mandelic acid is a natural product obtained from bitter almonds.
Chemical propertiesWhite crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, from bitter almond.
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
  1. A chiral resolver.

  2. Used in organic synthesis and pharmaceutical industry

  3. Reagents for the analysis of bases, alcohols by ester analysis, and α-alkylation by stereoselective dioxopentyl ring analysis


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