Phenoxyacetic acid structure
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Common Name | Phenoxyacetic acid | ||
|---|---|---|---|---|
| CAS Number | 122-59-8 | Molecular Weight | 152.147 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 285.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C8H8O3 | Melting Point | 98-100 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 115.1±13.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of Phenoxyacetic acidPhenoxyacetic acid is an endogenous metabolite. |
| Name | phenoxyacetic acid |
|---|---|
| Synonym | More Synonyms |
| Description | Phenoxyacetic acid is an endogenous metabolite. |
|---|---|
| Related Catalog |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 285.0±0.0 °C at 760 mmHg |
| Melting Point | 98-100 °C(lit.) |
| Molecular Formula | C8H8O3 |
| Molecular Weight | 152.147 |
| Flash Point | 115.1±13.3 °C |
| Exact Mass | 152.047348 |
| PSA | 46.53000 |
| LogP | 1.34 |
| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
| Index of Refraction | 1.541 |
| InChIKey | LCPDWSOZIOUXRV-UHFFFAOYSA-N |
| SMILES | O=C(O)COc1ccccc1 |
| Stability | Stable. Substances to be avoided include strong bases, strong oxidizing agents. Combustible. |
| Water Solubility | 0.1-0.5 g/100 mL at 17 ºC |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302-H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xn:Harmful |
| Risk Phrases | R22;R36/37/38 |
| Safety Phrases | S26-S36-S37/39 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | AJ2230000 |
| HS Code | 2942000000 |
| Precursor 10 | |
|---|---|
| DownStream 10 | |
| HS Code | 2918990090 |
|---|---|
| Summary | 2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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Synthesis, characterization and antibacterial activity of azomethine derivatives derived from 2-formylphenoxyacetic acid.
Molecules 12(2) , 245-54, (2007) A series of eight new azomethine derivatives were synthesized by reacting 2-formylphenoxyacetic acid with aromatic amines. The chemical structures of these compounds were confirmed by means of 1H-NMR,... |
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Penicillin V acylase from Pectobacterium atrosepticum exhibits high specific activity and unique kinetics.
Int. J. Biol. Macromol. 79 , 1-7, (2015) Penicillin V acylases (PVAs, E.C.3.5.11) belong to the Ntn hydrolase super family of enzymes that catalyze the deacylation of the side chain from phenoxymethyl penicillin (penicillin V). Penicillin ac... |
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Correlations between chromatographic parameters and bioactivity predictors of potential herbicides.
J. Chromatogr. Sci. 52 , 676-84, (2014) Different liquid chromatography techniques, including reversed-phase liquid chromatography on Purosphere RP-18e, IAM.PC.DD2 and Cosmosil Cholester columns and micellar liqud chromatography with a Puro... |
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Name: Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
Source: NCGC
External Id: SNCA-p-activity-luciferase
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu...
Source: 824
External Id: CYP273
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Name: Octanol-water partition coefficient, log P of the compound
Source: ChEMBL
Target: N/A
External Id: CHEMBL3256050
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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Name: Cyclohexanol-water partition coefficient, log P of the compound
Source: ChEMBL
Target: N/A
External Id: CHEMBL3256054
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Name: Hedgehog Measured in Biochemical System Using Plate Reader - 2070-01_Inhibitor_Single...
Source: Broad Institute
Target: hedgehog, isoform A [Drosophila melanogaster]
External Id: 2070-01_Inhibitor_SinglePoint_HTS_Activity
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|
Name: qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity
Source: NCGC
External Id: HERG01
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Name: qHTS for Inhibitors of TGF-b: Cytotox Counterscreen
Source: NCGC
Target: N/A
External Id: SMAD3201
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Name: uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay
Source: Burnham Center for Chemical Genomics
Target: cystic fibrosis transmembrane conductance regulator [Homo sapiens]
External Id: SBCCG-A764-CF-PAF-Primary-Assay
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| PHENOXYETHYLBROMIDE |
| 1-phenoxy-2-bromoethane |
| phenoxy acetic acid |
| PhO-CH2COOH |
| 2-phenoxy-ethyl bromide |
| 2-bromoethyl phenyl ether |
| B-BROMOPHENETOLE |
| Phenylium |
| 1-bromo-2-phenyloxyethane |
| Glycolic acid phenyl ether |
| phenoxy-acetic acid |
| MFCD00004296 |
| 2-phenoxyacetic acid |
| 2-Phenoxy-acetic acid |
| EINECS 204-556-7 |
| 1-bromo-2-phenoxyethane |
| Phenoxyacetic acid |