Organic Acids

Organic compounds with acidic properties, organic acids are generally weak acids incapable of complete dissociation in water. Available in a range of chemical compositions and acid strengths, they can be used for various industrial and everyday applications.

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3,271 – 3,285 of 4,347 results

3,271

eMolecules 1314397-71-1 | 1-(DIFLUOROMETHYL)CYCLOPROPANECARBOXYLIC ACID | AstaTech | MFCD20230593 | 136.098 | C5H6F2O2 | 95.000 | OC(=O)C1(CC1)C(F)F | 0.1g | 771348296

1-(DIFLUOROMETHYL)CYCLOPROPANECARBOXYLIC ACID | AstaTech | 1314397-71-1 | MFCD20230593 | 136.098 | C5H6F2O2 | 95.000 | OC(=O)C1(CC1)C(F)F | 0.1g | 771348296

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3,272

Aqua Solutions Citric Acid/surfactant Reagent(2.9 Liters)

Citric Acid/surfactant Reagent(2.9 Liters)

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3,273

eMolecules Ambeed / Cycloheptane carboxylic acid / 1g / 524986406 / A102010 / / 1460-16-8 / MFCD00004152 / 142.198 / C8H14O2

Ambeed / Cycloheptane carboxylic acid / 1g / 524986406 / A102010 / / 1460-16-8 / MFCD00004152 / 142.198 / C8H14O2

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3,274

eMolecules 32833-96-8 | 2-(Dimethylamino)-2-oxoacetic acid | Ambeed | MFCD01971023 | 117.104 | C4H7NO3 | 97.000 | CN(C)C(=O)C(O)=O | 1g | 533498148

2-(Dimethylamino)-2-oxoacetic acid | Ambeed | 32833-96-8 | MFCD01971023 | 117.104 | C4H7NO3 | 97.000 | CN(C)C(=O)C(O)=O | 1g | 533498148

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3,275

eMolecules 4942-47-6 | 1-Adamantaneacetic acid | Ambeed194.274 | C12H18O2 | 98.000 | OC(=O)CC12CC3CC(CC(C3)C1)C2 | 1g | 490509199

1-Adamantaneacetic acid | Ambeed | 4942-47-6194.274 | C12H18O2 | 98.000 | OC(=O)CC12CC3CC(CC(C3)C1)C2 | 1g | 490509199

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3,276

eMolecules 30100-16-4 | Boc-8-aoc-oh | Ambeed | MFCD00270350 | 259.346 | C13H25NO4 | 97.000 | CC(C)(C)OC(=O)NCCCCCCCC(O)=O | 250mg | 552559311

Boc-8-aoc-oh | Ambeed | 30100-16-4 | MFCD00270350 | 259.346 | C13H25NO4 | 97.000 | CC(C)(C)OC(=O)NCCCCCCCC(O)=O | 250mg | 552559311

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3,277

eMolecules Ambeed / Boc-Gly-Pro-OH / 250mg / 525109152 / A192072 / / 14296-92-5 / MFCD00057234 / 272.301 / C12H20N2O5

Ambeed / Boc-Gly-Pro-OH / 250mg / 525109152 / A192072 / / 14296-92-5 / MFCD00057234 / 272.301 / C12H20N2O5

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3,278

Medchemexpress LLC Citric acid triammonium | 3458-72-8 | 99.9% | 100 G

Citric acid triammonium is formed by Citric acid reacting with ammonia in a molar ratio of 1:3. It can be utilized as a carbon source for preparing carbon quantum dots (CDs). When citric acid triammonium contains higher nitrogen components, it may enhance the nitrogen-based functional groups in CDs, leading to more efficient emission-color tunability.

Molecular weight: 243.22
Formula: C6H17N3O7
Appearance: Solid
Color: White to off-white
SMILES: O=C(CC(C(O)=O)(O)CC(O)=O)O.[3NH3]
Shipping: Room temperature in continental US; may vary elsewhere
Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

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3,279

eMolecules 2450-31-9 | Ambeed | Tetracosanedioic acid | 1g | 632810513 | A737455 | MFCD00002809 | 398.628 | C24H46O4

Ambeed | 2-Nitro-1H-pyrrole | 250mg | 553232023 | A562079 | 5919-26-6 | MFCD12923841 | 112.088 | C4H4N2O2

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3,280

eMolecules 2248271-56-7 | 4-{[(tert-butoxy)carbonyl]amino}-2-chloro-6-fluorobenzoic acid | Synthonix289.690 | C12H13ClFNO4 | 98.000 | CC(C)(C)OC(=O)Nc1cc(F)c(C(O)=O)c(Cl)c1 | 10mg | 794075932

4-{[(tert-butoxy)carbonyl]amino}-2-chloro-6-fluorobenzoic acid | Synthonix | 2248271-56-7289.690 | C12H13ClFNO4 | 98.000 | CC(C)(C)OC(=O)Nc1cc(F)c(C(O)=O)c(Cl)c1 | 10mg | 794075932

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3,281

eMolecules 776309-04-7 | Medchem Express | JTT 551 | 5mg | 771358952 | HY-19779 | 605.86 | C34H43N3O3S2

Medchem Express | JTT 551 | 5mg | 771358952 | HY-19779 | 776309-04-7 | 605.860 | C34H43N3O3S2

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3,282

Aobchem 3-(Propylthio)benzoic acid | ≥95% | CAS 110208-00-9 | C10H12O2S | 500mg

3-(Propylthio)benzoic acid | ≥95% | CAS 110208-00-9 | C10H12O2S | 500mg

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3,283

Apexbio Technology LLC Urotensin-II-114-124-human-TFA

Urotensin II (114-124 human) TFA (CAS No 251293-28-4) is a peptide fragment primarily utilized in cardiovascular and neurological research It originates from human urotensin II a potent vasoactive peptide involved in various physiological processes primarily acting through the G protein-coupled urotensin II receptor (UT) This interaction influences cellular pathways related to vasoconstriction and vascular smooth muscle proliferation In vitro this fragment functions in the nanomolar to low micromolar range demonstrating significant potency in cellular assays Typically employed in cell models and animal studies it aids in exploring cardiovascular dysfunction evaluating potential therapeutic agents and drug screening protocols Experimental concentrations typically depend on the specific research design ensuring flexibility for diverse investigative focuses