- Min.Order :100 Gram
- Purity: 99%
- Payment Terms : L/C,D/A,D/P,T/T,Other
Keywords
RARECHEM AL BO 0133 P-METHOXY-A-CARBOXYTOLUENE HOMO-P-ANISIC ACID
Quick Details
- Appearance:white to light yellow crystalline powder
- Application: 104-01-8
- PackAge:1g;5g;10g;25g;50g;100g;500g;1KG;5KG,25kg,50kg or as customers request
- ProductionCapacity:100|Kilogram|Month
- Storage:2-8, cold storage, to avoid light storage.
- Transportation:BY SEA /BY AIR /BY COURIER
Superiority:
Exhibition in shanghai
Our Laboratoy
Our factory
Package & Shipment
Details:
| 4-Methoxyphenylacetic acid Basic information |
| Product Name: | 4-Methoxyphenylacetic acid |
| Synonyms: | ASISCHEM D13364;LABOTEST-BB LT00848110;HOMOANISIC ACID;HOMO-P-ANISIC ACID;4-METHOXYPHENYLACETIC ACID;P-METHOXY-A-CARBOXYTOLUENE;P-METHOXYPHENYLACETIC ACID;RARECHEM AL BO 0133 |
| CAS: | 104-01-8 |
| MF: | C9H10O3 |
| MW: | 166.17 |
| EINECS: | 203-166-4 |
| Product Categories: | Aromatic Phenylacetic Acids and Derivatives;pharmacetical;Building Blocks;C9;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks |
| Mol File: | 104-01-8.mol |
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| 4-Methoxyphenylacetic acid Chemical Properties |
| mp | 84-86 °C(lit.) |
| bp | 140 °C3 mm Hg(lit.) |
| Fp | 193°C |
| Water Solubility | 6 g/L (20 ºC) |
| BRN | 1101737 |
| CAS DataBase Reference | 104-01-8(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzeneacetic acid, 4-methoxy-(104-01-8) |
| EPA Substance Registry System | Benzeneacetic acid, 4-methoxy-(104-01-8) |
| Safety Information |
| Hazard Codes | Xn,Xi |
| Risk Statements | 22-36/37/38-20/21/22 |
| Safety Statements | 26-36 |
| WGK Germany | 3 |
| RTECS | AI8960000 |
| Hazard Note | Irritant |
| HS Code | 29189090 |
| MSDS Information |
| Provider | Language |
|---|---|
| 4-Methoxyphenylacetic acid | English |
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| 4-Methoxyphenylacetic acid Usage And Synthesis |
| Chemical Properties | white to light yellow crystalline powder and |
| General Description | Pale yellow or off white colored flakes. Severely irritates skin and eyes. May be toxic by ingestion. |
| Reactivity Profile | Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 4-Methoxyphenylacetic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. |
| Health Hazard | TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution. |
| Fire Hazard | Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. |
Service we provide:
1. Mixed container, we can mix different items in one container.
2. Quality control, before shipment, free sample for test. after shipment, keep sample for 3 years
3. Prompt shipment with professional documents
4. Packing as your request, with photo before shipment
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