Chemical Acids
| Packaging Size | 25 Kg, 25 KG |
| Form | Powder |
| Packaging Type | 25 PAPER BAG |
| Pack Type | PAPER BAG |
| Country of Origin | Made in India |
We are providing an excellent quality array of Fumaric Acid to our prestigious clients at very affordable rates within committed period of time.
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Specification: Specification CAS Registry Number 110-17-8 ATC code D05AX01 ChEBI CHEBI:18012 ChEMBL ChEMBL 503160 ChemSpider 10197150 DrugBank DB04299 EC number 203-743-0 InChI[show] Jmol-3D images Image KEGG C00122 SMILES[show] UNII 88XHZ13131 Properties Chemical formula C4H4O4 Molar mass 116.07 g·mol−1 Appearance White solid Density 1.635 g/cm3 Melting point 287 °C (549 °F; 560 K) (decomp)[2] Solubility in water 4.3 g/L at 20°C[1] Acidity (pKa) pka1 = 3.03, pka2 = 4.44 Hazards EU classification Irritant (Xi) R-phrases R36 S-phrases (S2)-S26 NFPA 704 120 Related compounds Related carboxylic acids maleic acid succinic acid crotonic acid Related compounds fumaryl chloride fumaronitrile dimethyl fumarate iron(II) fumarate
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| Packaging Size | 30 kg |
| Form | Liquid |
| Grade Standard | Industrial |
| Color | White |
| Packaging Type | Bottles |
| Application | Acidity Regulators, Pharmaceutical Intermediates |
| Packing Size | BARREL,CARBO |
Acetic acid /əˈsiːtᵻk/, systematically named ethanoic acid /ˌɛθəˈnoʊᵻk/, is a colourless liquid organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2). When undiluted, it is sometimes called glacial acetic acid. Vinegar is roughly 3–9% acetic acid by volume, making acetic acid the main component of vinegar apart from water. Acetic acid has a distinctive sour taste and pungent smell. In addition to household vinegar, it is mainly produced as a precursor to polyvinyl acetate and cellulose acetate. Although it is classified as a weak acid, concentrated acetic acid is corrosive and can attack the skin.
Acetic acid is the second simplest carboxylic acid (after formic acid) and consists of two small functional groups, an acetyl group (sometimes symbolized as Ac) and a hydroxyl group (AcOH); it can also be viewed as a methyl group and a carboxyl group linked. It is an important chemical reagent and industrial chemical, used primarily in the production of cellulose acetate for photographic film, polyvinyl acetate for wood glue, and synthetic fibres and fabrics. In households, diluted acetic acid is often used in descaling agents. In the food industry, acetic acid is controlled by the food additive code E260 as an acidity regulator and as a condiment. As a food additive it is approved for usage in many countries, including Canada,[6] the European Union,[7] the United States,[8] Australia and New Zealand.[9] In biochemistry, the acetyl group, derived from acetic acid, is fundamental to all forms of life. When bound to coenzyme A, it is central to the metabolism of carbohydrates and fats.
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| Form | Powder |
| Usage | Industrial |
| Grade Standard | Technical Grade |
| Packaging Size | 50KG |
| Packaging Type | PLASTIC BAG |
| Purity | 99% |
| Chemical Formula | C2H3ClO2 |
We are among the leading organizations in the industry for offering an extensive array of Mono Chloro Acetic Acids to our esteemed clients. These products are prepared from only high quality components.
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Illustrative of its usefulness in organic chemistry is the O-alkylation of salicylaldehyde with chloroacetic acid, followed by decarboxylation of the resulting ether, producing benzofuran.[4] In industry, chloroacetic acid is used in the production of a wide variety of useful compounds; e.g., drugs, dyes, pesticides.[3] Most reactions take advantage of the high reactivity of the C–Cl bond. It is the precursor to the herbicide glyphosate, and the herbicides MCPA (2-methyl-4-chlorophenoxyacetic acid) and dimethoate are prepared by alkylation with chloroacetic acid. Chloroacetic acid is converted to chloroacetyl chloride, a precursor to adrenaline (epinephrine). Displacement of chloride by sulfide gives thioglycolic acid, which is used as a stabilizer in PVC and a component in some cosmetics. In its largest-scale application, chloroacetic acid is used to prepare the thickening agent carboxymethyl cellulose and carboxymethyl starch.
Like other chloroacetic acids and related halocarbons, chloroacetic acid is a hazardous alkylating agent. The LD50 for rats is 76 mg/kg.(3)
Chloroacetic acid easily penetrates skin and mucous membranes and interferes with cellular energy production. Initial dermal exposure to high concentrations (e.g., 80% solution) may not appear very damaging at first, however systemic poisoning may present within hours. Exposure can be fatal if greater than 6% body surface area is exposed to chloroacetic acid. The sodium salt does not penetrate the skin as well as the acid but can be as damaging given a longer duration and greater surface area of exposure.
Upon exposure to chloroacetic acid, immediate decontamination should be commenced by rinsing the affected area with water or bicarbonate solution in order to neutralize the acid and prevent further skin absorption
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| Usage/Application | Industrial |
| Grade Standard | Chemical Grade |
| Form Of Chemicals | Powder |
| Boiling Point | 163.5 C |
| Cas-No | 107-92-6 |
| Molecular Formula | C4H8O2 |
IUPAC name Butanoic acid
| Other names Butyric acid, 1-Propanecarboxylic acid, Propanecarboxylic acid, C4:0 (Lipid numbers) | |
| Identifiers | |
|---|---|
| CAS Number | 107-92-6 |
| ChEBI | CHEBI:30772 |
| ChEMBL | ChEMBL14227 |
| ChemSpider | 259 |
| DrugBank | DB03568 |
| EC Number | 203-532-3 |
| IUPHAR/BPS | 1059 |
| Jmol 3D model | Interactive image Interactive image |
| KEGG | C00246 |
| MeSH | Butyric+acid |
| PubChem | 264 |
| RTECS number | ES5425000 |
| UNII | 40UIR9Q29H |
| UN number | 2820 |
| InChI[show] | |
| SMILES[show] | |
| Properties | |
| Chemical formula | C 3H 7COOH |
| Molar mass | 88.11 g·mol−1 |
| Appearance | Colorless liquid |
| Odor | Unpleasant and obnoxious |
| Density | 1.135 g/cm3 (−43 °C)[1] 0.9528 g/cm3 (25 °C)[2] |
| Melting point | −5.1 °C (22.8 °F; 268.0 K)[2] |
| Boiling point | 163.75 °C (326.75 °F; 436.90 K)[2] |
| Sublimation conditions | Sublimes at −35 °C ΔsublHo = 76 kJ/mol[3] |
| Solubility in water | Miscible |
| Solubility | Slightly soluble in CCl4[4] Miscible with ethanol, ether |
| log P | 0.79[4] |
| Vapor pressure | 0.112 kPa (20 °C)[5] 0.74 kPa (50 °C) 9.62 kPa (100 °C)[3] |
| Henry''s law constant (kH) | 5.35·10−4 L·atm/mol[4] |
| Acidity (pKa) | 4.82[4] |
| Thermal conductivity | 1.46·105 W/m·K |
| Refractive index (nD) | 1.398 (20 °C)[2] |
| Viscosity | 1.814 cP (15 °C)[6] 1.426 cP (25 °C)[4] |
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| Form | Powder |
| Packaging Size | 50 KG |
| Type | Anhydrous, Monohydrate |
| ||
| Names | ||
|---|---|---|
| IUPAC name2-hydroxypropane-1,2,3-tricarboxylic acid | ||
| Other names citric acid | ||
| Identifiers | ||
| CAS Number | 77-92-9 | |
| ChEBI | CHEBI:30769 | |
| ChEMBL | ChEMBL1261 | |
| ChemSpider | 305 | |
| DrugBank | DB04272 | |
| EC Number | 201-069-1 | |
| IUPHAR/BPS | 2478 | |
| Jmol 3D model | Interactive image | |
| D00037 | ||
| 22230 (monohydrate) 311, 22230 (monohydrate) | ||
| GE7350000 | ||
| XF417D3PSL | ||
| Properties | ||
| Chemical formula | C6H8O7 | |
| Molar mass | 192.12 g·mol−1 | |
| Appearance | crystalline white solid | |
| Odor | odorless | |
| Density | 1.665 g/cm3 (anhydrous) 1.542 g/cm3 (18 °C, monohydrate) | |
| Melting point | 156 °C (313 °F; 429 K) | |
| Boiling point | 310 °C (590 °F; 583 K) decomposes from 175 °C[1] | |
| Solubility in water | 117.43 g/100 mL (10 °C) 147.76 g/100 mL (20 °C) 180.89 g/100 mL (30 °C) 220.19 g/100 mL (40 °C) 382.48 g/100 mL (80 °C) 547.79 g/100 mL (100 °C)[2] | |
| Solubility | soluble in alcohol, ether, ethyl acetate, DMSO insoluble in C6H6, CHCl3, CS2, toluene[1] | |
| Solubility in ethanol | 62 g/100 g (25 °C)[1] | |
| Solubility in amyl acetate | 4.41 g/100 g (25 °C)[1] | |
| Solubility in diethyl ether | 1.05 g/100 g (25 °C)[1] | |
| Solubility in 1,4-Dioxane | 35.9 g/100 g (25 °C)[1] | |
| log P | -1.64 | |
| Acidity (pKa) | pKa1 = 3.13[3] pKa2 = 4.76[3] pKa3 = 6.39,[4] 6.40[5] | |
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