Mandelic acid

Modify Date: 2024-01-02 13:16:17

Mandelic acid Structure
Mandelic acid structure
Common Name Mandelic acid
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
GHS05
Signal Word Danger

 Use of Mandelic acid


D-(-)-Mandelic acid is a natural compound isolated from bitter almonds.

 Names

Name D-(-)-Mandelic acid
Synonym More Synonyms

 Mandelic acid Biological Activity

Description D-(-)-Mandelic acid is a natural compound isolated from bitter almonds.
Related Catalog

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
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

 Safety Information

Symbol GHS05
GHS05
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

 Synthetic Route

 Customs

HS Code 2918199090
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%

 Articles35

More Articles
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...

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...

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...

 Synonyms

(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
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