Mandelic acid structure
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Common Name | Mandelic acid | ||
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CAS Number | 611-71-2 | Molecular Weight | 152.15 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 321.8±22.0 °C at 760 mmHg | |
Molecular Formula | C8H8O3 | Melting Point | 130-134ºC | |
MSDS | Chinese USA | Flash Point | 162.6±18.8 °C | |
Symbol |
GHS05 |
Signal Word | Danger |
Use of Mandelic acidD-(-)-Mandelic acid is a natural compound isolated from bitter almonds. |
Name | D-(-)-Mandelic acid |
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Synonym | More Synonyms |
Description | D-(-)-Mandelic acid is a natural compound isolated from bitter almonds. |
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Related Catalog |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 321.8±22.0 °C at 760 mmHg |
Melting Point | 130-134ºC |
Molecular Formula | C8H8O3 |
Molecular Weight | 152.15 |
Flash Point | 162.6±18.8 °C |
Exact Mass | 152.047348 |
PSA | 57.53000 |
LogP | 0.92 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.591 |
Symbol |
GHS05 |
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Signal Word | Danger |
Hazard Statements | H318 |
Precautionary Statements | P280-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
Hazard Codes | Xi |
Risk Phrases | R41 |
Safety Phrases | S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 1 |
HS Code | 2918199090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2918199090 |
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Summary | 2918199090 other carboxylic acids with alcohol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% |
Simultaneous determination of aromatic acid metabolites of styrene and styrene-oxide in rat urine by gas chromatography-flame ionization detection.
J. Anal. Toxicol. 36(5) , 312-8, (2012) A convenient and reliable gas chromatographic method was developed for the simultaneous determination of six aromatic acid metabolites of styrene and styrene-oxide in rat urine; i.e., benzoic (BA), ph... |
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Chiral separation of D,L-mandelic acid through cellulose membranes.
Chirality 23(5) , 379-82, (2011) This work reports the chiral separation of D,L-mandelic acid with cellulose membranes. Cellulose was chosen as membrane material because it possesses multichiral carbon atoms in its molecular structur... |
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DNA damage and susceptibility assessment in industrial workers exposed to styrene.
J. Toxicol. Environ. Health A 75(13-15) , 735-46, (2012) Styrene is a widely used chemical in the manufacture of synthetic rubber, resins, polyesters, and plastics. The highest levels of human exposure to styrene occur during the production of reinforced pl... |
(S)-(+)-2-hydroxy-2-phenylacetic acid |
S-mandelic acid |
(-)-mandelic acid |
(S)-2-Hydroxy-2-phenylacetic acid |
(2R)-hydroxy(phenyl)ethanoic acid |
D-mandelic acid |
(S)-(+)-Amygdalic Acid |
R-(-)-Mandelic acid |
L-MANDELIC ACID |
(R)-(-)-Mandelic acid |
(R)-(-)-Amygdalic Acid |
(S)-mandelic acid |
L-mandelate |
S-(+)-Mandelic acid |
(2R)-Hydroxy(phenyl)acetic acid |
Benzeneacetic acid, α-hydroxy-, (αS)- |
(S)-α-Hydroxyphenylacetic acid |
(-)-(R)-mandelic acid |
2-phenyl-2-hydroxyethanoic acid |
Benzeneacetic acid, α-hydroxy-, (αR)- |
(+)-L-MANDELIC ACID |
MFCD00064251 |
(+)-MANDELIC ACID |
(S)-Mandelate |
(R)-MANDELIC ACID |
(2S)-Hydroxy(phenyl)acetic acid |
Mandelic acid |
Benzeneacetic acid, α-hydroxy-, (R)- |
(+)-(S)-MANDELIC ACID |
hydroxyphenylacetic acid |
(S)-(+)-Mandelic acid |
Benzeneacetic acid, α-hydroxy-, (S)- |
phenyl-hydroxy-acetic acid |
D-(-)-Mandelic acid |
benzeneacetic acid, a-hydroxy-, (aR)- |
EINECS 210-276-6 |
(R)-(-)-Mandelicacid |
L-(+)-Mandelic Acid |
(R)-(−)-Mandelic acid |
(2S)-hydroxy(phenyl)ethanoic acid |
(D)-(-)-Mandelicacid |