(S)-(+)-Mandelic acid structure
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Common Name | (S)-(+)-Mandelic acid | ||
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CAS Number | 17199-29-0 | 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 | 131-134 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 162.6±18.8 °C |
Use of (S)-(+)-Mandelic acid(S)-Mandelic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | (S)-mandelate |
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Synonym | More Synonyms |
Description | (S)-Mandelic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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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 | 131-134 °C(lit.) |
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 |
Water Solubility | 100 g/L (25 ºC) |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S22-S24/25-S37/39-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2918199090 |
Precursor 0 | |
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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 |
EINECS 241-240-8 |
S-mandelic acid |
(S)-2-Hydroxy-2-phenylacetic acid |
(S)-(+)-Amygdalic Acid |
L-MANDELIC ACID |
(S)-mandelic acid |
L-mandelate |
S-(+)-Mandelic acid |
Benzeneacetic acid, α-hydroxy-, (αS)- |
(S)-α-Hydroxyphenylacetic acid |
2-phenyl-2-hydroxyethanoic acid |
(+)-L-MANDELIC ACID |
(+)-MANDELIC ACID |
(S)-Mandelate |
(2S)-Hydroxy(phenyl)acetic acid |
Mandelic acid |
(+)-(S)-MANDELIC ACID |
hydroxyphenylacetic acid |
(S)-(+)-Mandelic acid |
Benzeneacetic acid, α-hydroxy-, (S)- |
phenyl-hydroxy-acetic acid |
MFCD00004495 |
L-(+)-Mandelic Acid |
(2S)-hydroxy(phenyl)ethanoic acid |