Chemical Properties of Mandelic acid (CAS 90-64-2)

Mandelic acid

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InChI
InChI=1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)
InChI Key
IWYDHOAUDWTVEP-UHFFFAOYSA-N
Formula
C8H8O3
SMILES
O=C(O)C(O)c1ccccc1
Molecular Weight1
152.15
CAS
90-64-2
Other Names
  • Benzeneacetic acid, «alpha»-hydroxy-
  • «alpha»-Hydroxy-«alpha»-toluic acid
  • «alpha»-Hydroxyphenylacetic acid
  • p-Mandelic acid
  • Almond acid
  • Amygdalic acid
  • Amygdalinic acid
  • Phenylglycolic acid
  • Phenylhydroxyacetic acid
  • Uromaline
  • dl-Mandelic acid
  • «alpha»-Toluic acid, «alpha»-hydroxy-
  • Glycolic acid, phenyl-
  • Racemic mandelic acid
  • Kyselina 2-fenyl-2-hydroxyethanova
  • Kyselina mandlova
  • Paramandelic acid
  • «alpha»-Phenylhydroxyacetic acid
  • Benzoglycolic acid
  • Hydroxy(phenyl)acetic acid
  • Benzeneacetic acid, «alpha»-hydroxy-, (.+/-.)-
  • (.+/-.)-alpha-Hydroxybenzeneacetic acid
  • (.+/-.)-Mandelic acid
  • (RS)-Mandelic acid
  • 2-Phenyl-2-hydroxyacetic acid
  • 2-Phenylglycolic acid
  • DL-Hydroxy(phenyl)acetic acid
  • NSC 7925
  • 114-21-6
  • 530-31-4
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Physical Properties

Property Value Unit Source
Δf -276.11 kJ/mol Joback Calculated Property
Δfgas -394.24 kJ/mol Joback Calculated Property
Δfus 16.77 kJ/mol Joback Calculated Property
Δvap 75.39 kJ/mol Joback Calculated Property
log10WS -1.10 Crippen Calculated Property
logPoct/wat 0.805 Crippen Calculated Property
McVol 113.130 ml/mol McGowan Calculated Property
Pc 5102.04 kPa Joback Calculated Property
Inp 1487.00 NIST
Tboil 646.91 K Joback Calculated Property
Tc 844.13 K Joback Calculated Property
Tfus 392.00 ± 1.50 K NIST
Vc 0.413 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [278.92; 319.12] J/mol×K [646.91; 844.13] Show Hide
Cp,gas 278.92 J/mol×K 646.91 Joback Calculated Property
Cp,gas 286.85 J/mol×K 679.78 Joback Calculated Property
Cp,gas 294.26 J/mol×K 712.65 Joback Calculated Property
Cp,gas 301.16 J/mol×K 745.52 Joback Calculated Property
Cp,gas 307.59 J/mol×K 778.39 Joback Calculated Property
Cp,gas 313.57 J/mol×K 811.26 Joback Calculated Property
Cp,gas 319.12 J/mol×K 844.13 Joback Calculated Property
Cp,solid 199.20 J/mol×K 323.00 NIST
η [0.0000249; 0.0084829] Pa×s [362.91; 646.91] Show Hide
η 0.0084829 Pa×s 362.91 Joback Calculated Property
η 0.0018322 Pa×s 410.24 Joback Calculated Property
η 0.0005434 Pa×s 457.58 Joback Calculated Property
η 0.0002024 Pa×s 504.91 Joback Calculated Property
η 0.0000893 Pa×s 552.24 Joback Calculated Property
η 0.0000448 Pa×s 599.58 Joback Calculated Property
η 0.0000249 Pa×s 646.91 Joback Calculated Property
ΔfusH 25.52 kJ/mol 392.00 NIST

Similar Compounds

Benzeneacetic acid, «alpha»-hydroxy-, (S)-. Mandelic acid. p-Chloromandelic acid. 4-Fluoromandelic acid. Methyl mandelate. Benzeneacetic acid, «alpha»-hydroxy-, ethyl ester, (R)-. Ethyl mandelate. Benzeneacetic acid, «alpha»-methoxy-, (S)-. Benzeneacetic acid, «alpha»-methoxy-, (.+/-.)-. Benzeneacetic acid, «alpha»-methoxy-, (.+/-.)-. (R)-(-)-«alpha»-Methoxyphenylacetic acid. Mandelamide. Benzeneacetic acid, «alpha»-hydroxy-4-methoxy-, methyl ester. 1,2-Ethanediol, 1-phenyl-. 3-Hydroxymandelic acid, methyl ester.

Find more compounds similar to Mandelic acid.

Sources

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