Identification | More | [Name]
(3,4-Dimethoxyphenyl)acetic acid | [CAS]
93-40-3 | [Synonyms]
3,4-DIMETHOXYPHENYLACETIC ACID AKOS 90105 AKOS BBS-00003748 ASISCHEM P20560 HOMOVERATRIC ACID RARECHEM AL BO 0125 (3,4-dimethoxyphenyl)-aceticaci 3,4-(Dimethoxy)benzeneacetic acid 3,4-dimethoxy-benzeneaceticaci 3,4-dimethoxybenzeneaceticacid Benzeneacetic acid, 3,4-dimethoxy- Homoveratricacidhomoveratrumicacid HOMOVERATRIC ACID CRYSTALLINE 2-(3,4-dimethoxyphenyl)acetic acid 3-(3,4-dimethoxy phenyl)acetic acid 3,4-DIMETHOXYPHENYLACETIC ACID/HOMOVERATRIC ACID Homoveratrumic acid | [EINECS(EC#)]
202-244-5 | [Molecular Formula]
C10H12O4 | [MDL Number]
MFCD00004335 | [Molecular Weight]
196.2 | [MOL File]
93-40-3.mol |
Chemical Properties | Back Directory | [Appearance]
white to beige powder | [Melting point ]
96-98 °C (lit.) | [Boiling point ]
293.08°C (rough estimate) | [density ]
1.2166 (rough estimate) | [refractive index ]
1.5430 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Powder | [pka]
pK1:4.333 (25°C) | [color ]
White to beige | [Water Solubility ]
SOLUBLE | [BRN ]
1110282 | [InChIKey]
WUAXWQRULBZETB-UHFFFAOYSA-N | [LogP]
1.242 | [CAS DataBase Reference]
93-40-3(CAS DataBase Reference) | [NIST Chemistry Reference]
Acetic acid, 3,4-dimethoxyphenyl-(93-40-3) | [EPA Substance Registry System]
93-40-3(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . R22:Harmful if swallowed. | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . S36/37:Wear suitable protective clothing and gloves . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
AH0675000
| [Hazard Note ]
Irritant | [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29189090 |
Hazard Information | Back Directory | [Chemical Properties]
white to beige powder | [Uses]
Homoveratric Acid is a dopamine metabolite that inhibits brain mitochondrial respiration via monoamine oxidase/H2O2-dependent or non-dependent pathway. | [Definition]
ChEBI: Homoveratric acid is a phenylacetic acid substituted at positions 3 and 4 by methoxy groups. It has a role as a human urinary metabolite and a human xenobiotic metabolite. It is a dimethoxybenzene and a member of phenylacetic acids. | [Synthesis Reference(s)]
Organic Syntheses, Coll. Vol. 2, p. 333, 1943 The Journal of Organic Chemistry, 15, p. 548, 1950 DOI: 10.1021/jo01149a016 | [Purification Methods]
Crystallise homoveratric acid from H2O or *C6H6/ligroin. The amide has m 142o (from H2O). [Beilstein 10 H 409, 10 I 197, 10 II 268, 10 III 1459, 10 IV 1509.] |
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