Search results

Create the page "Acids" on this wiki! See also the search results found.

• Filtration
  ...be used to remove most impurities, though it is not compatible with strong acids and oxidizing solutions.
  3 KB (467 words) - 21:24, 2 December 2018
• Reagent bottle
  ...glass bottle is commonly used for storing organic solvents, though mineral acids are also usually stored in such bottles. Transparent bottles tend to be use ...unsuitable for storing corrosive chemicals, especially volatile ones, like acids, as the metal lid will rust.
  9 KB (1,411 words) - 14:43, 26 November 2022
• NaK
  ...ediately on contact with air. It reacts violently with water, alcohols and acids.
  2 KB (307 words) - 21:20, 24 April 2020
• Diatomaceous earth
  ...earth consists mostly of [[silicon dioxide]] and resists corrosion by most acids, except for [[hydrofluoric acid]].
  2 KB (269 words) - 14:12, 27 June 2018
• Zeolite
  Zeolites are attacked by strong acids and bases.
  1 KB (197 words) - 16:19, 10 December 2017
• Potassium bisulfate
  ...turated acid, potassium bisulfate solutions have a much lower pH than many acids themselves, and should be treated with care. It may also release sulfuric a [[Category:Acids]]
  5 KB (587 words) - 10:50, 27 October 2019
• Ammonium sulfide
  | SolubleOther = Reacts with acids, bases<br>Soluble in liquid [[ammonia]], [[ethanol]], [[methanol]]
  6 KB (681 words) - 16:39, 1 March 2021
• Potassium bicarbonate
  | SolubleOther = Reacts with acids<br>Insoluble in alcohols, [[benzene]], [[chloroform]], [[toluene]] ...bonate, like its [[sodium bicarbonate|sodium counterpart]] will react with acids to form potassium salt of the said acid.
  5 KB (550 words) - 16:41, 3 July 2019
• Hydrogen cyanide
  HCN may be prepared quantitatively without the use of acids from Hg(CN)₂ by treatment with aluminium metal in water:<ref>G. [[Category:Acids]]
  10 KB (1,464 words) - 12:40, 26 January 2024
• Ammonium carbonate
  Reaction with acids gives ammonium salt of said acid and releases carbon dioxide:
  5 KB (606 words) - 14:02, 23 May 2021
• Sodium formate
  ...irritant and should be handled with proper protection. Contact with strong acids should be avoided as it will generate formic acid and carbon monoxide. Sodium formate should be stored in closed bottles, away from acids.
  4 KB (502 words) - 21:30, 12 August 2021
• Di-tert-butyl ether
  In closed bottles, away from light and strong acids. Since it resists auto-oxidation, ''t''-Bu2O does not form peroxides upon s
  4 KB (477 words) - 15:35, 1 March 2017
• Anthraquinone
  It resists the attack of many acids and bases.
  5 KB (576 words) - 22:31, 27 December 2023
• Chemistry Diamonds on Youtube
  [https://www.youtube.com/watch?v=l4mag18S6b8 Buying Acids OTC(in Australia)]
  9 KB (1,320 words) - 09:45, 9 January 2022
• Sodium bisulfite
  [[Category:Acids]]
  5 KB (543 words) - 17:07, 7 August 2017
• Mercury sulfide
  Mercury sulfide is resistant to the attack of most reagents, such as acids and bases.
  5 KB (576 words) - 21:34, 10 July 2022
• Methylamine
  Methylamine reacts with acids to form methylammonium salts, such as methylammmonium chloride (or methylam
  6 KB (801 words) - 21:56, 21 October 2020
• Acid
  ...y to donate [[proton]]s, or protonate other compounds. According to Lewis, acids are acceptors of electron pairs. == Strong and weak acids ==
  3 KB (535 words) - 21:07, 26 June 2017
• Devarda's alloy
  Devarda's alloy should be stored in closed bottles, away from bases, acids and oxidizers.
  2 KB (296 words) - 12:44, 10 September 2016
• Erowid
  .../chemistry/fc.acylation.tsoh.html Friedel-Crafts Acylation with Carboxylic Acids catalyzed by Tosic Acid]'''
  6 KB (941 words) - 16:51, 27 September 2016
• N-Methyl-2-pyrrolidone
  N-Methyl-2-pyrrolidone will react with acids to form salts. In closed bottles, away from acids.
  4 KB (419 words) - 21:36, 27 October 2020
• Hydroxylamine
  Hydroxylamine reacts with acids to give hydroxylammonium salts. Other acids, such as hydrochloric and phosphoric acids can also be used. The yield of this route is between 50-80%.<ref>Schoch, E.
  8 KB (1,041 words) - 16:34, 30 December 2023
• Methyl red
  Methyl red should be stored in closed amber bottles, away from light and acids.
  5 KB (626 words) - 21:47, 28 December 2023
• Succinic acid
  [[Category:Acids]] [[Category:Weak acids]]
  5 KB (582 words) - 12:29, 26 November 2022
• Brass
  Many acids, such as hydrochloric acid or sulfuric acid will only dissolve the zinc fro Brass objects should be kept away from acids and ammonia.
  6 KB (882 words) - 13:38, 20 November 2020
• Ammonium sulfite
  | SolubleOther = Reacts with acids<br>Insoluble in [[acetone]], [[ethanol]], [[toluene]] In sealed bottles, away from air or acids.
  4 KB (490 words) - 21:07, 13 October 2019
• Bromocresol green
  Bromocresol green is best kept in closed bottles, away from acids and ammonia.
  4 KB (459 words) - 19:14, 23 November 2023
• Potassium ferricyanide
  | SolubleOther = Soluble in acids<br>Slightly soluble in alcohols Reaction with very strong acids may release [[hydrogen cyanide]] which is exceedingly toxic.
  4 KB (476 words) - 19:36, 22 August 2020
• Amberlite
  In closed bottles, away from any volatile compounds, such as acids or ammonia.
  1 KB (182 words) - 13:50, 9 November 2019
• Methyl orange
  ...lour at the pH of a midstrength acid, it is usually used in titrations for acids. In closed bottles, away from acids and volatile compounds.
  4 KB (520 words) - 21:47, 28 December 2023
• Carboxylic acid
  Carboxylic acids can be classified under several categories: *Monocarboxylic acids: only have one -COOH group. Most are liquid at room temperature and have st
  4 KB (526 words) - 13:34, 31 December 2021
• Ammonium bisulfite
  [[Category:Acids]]
  4 KB (484 words) - 17:07, 6 August 2017
• Zinc acetate
  Zinc acetate should be stored in closed bottles, away from moisture and acids, in a well ventilated place.
  7 KB (851 words) - 14:26, 6 June 2019
• Stainless steel
  ...04L and 430 have shown to be more resistant. On the other hand, hydrohalic acids, such as [[hydrochloric acid]] will attack all types of stainless steel, mo Stainless steel objects should be kept away from hydrohalic acids and halogens. Periodically inspect SS objects for any signs of pitting corr
  6 KB (832 words) - 08:52, 23 September 2023
• Sodium methoxide
  | SolubleOther = Reacts with [[carboxylic acid]]s, halocarbons, mineral acids<br>Soluble in [[dimethyl sulfoxide|DMSO]], [[ethanol]], lipids, [[methanol]
  6 KB (759 words) - 20:55, 10 October 2019
• Benzoic acid
  [[Category:Acids]] [[Category:Carboxylic acids]]
  7 KB (907 words) - 21:15, 5 March 2024
• Steel
  ...ment. It shows good resistance to air oxidation, but presence of moisture, acids and or salts will cause steel to oxidize, and the apparition of rust. Iron-
  7 KB (1,131 words) - 14:21, 9 September 2020
• Aluminium isopropoxide
  6 KB (660 words) - 17:58, 8 August 2018
• Silver carbonate
  | SolubleOther = Reacts with acids<br>Insoluble in [[acetone]], liq. [[ammonia]], [[chloroform]], [[ethanol]], Like all other carbonates, silver carbonate will react with acids to give their respective silver salts and give off [[carbon dioxide]].
  5 KB (594 words) - 17:07, 6 July 2019
• Phosphorus pentachloride
  | SolubleOther = Reacts with alcohols, carboxylic acids<br>Soluble in [[benzene]], [[carbon disulfide]], [[carbon tetrachloride]], ...ide is a good chlorinating agent and is capable of chlorinating carboxylic acids to acyl chlorides:
  8 KB (1,001 words) - 21:15, 22 October 2022
• Phosphoryl chloride
  | SolubleOther = Reacts with alcohols, carboxylic acids<br>Soluble in benzoyl chloride, [[bromine]], bromoacetic acid, [[carbon dis
  6 KB (750 words) - 09:43, 15 August 2022
• Bronze
  ...ng a protective oxide coating which prevents further corrosion. Hydrohalic acids attack bronze in the presence of oxygen, while [[sulfuric acid]] attacks it Bronze items should be kept away from corrosive vapors, like acids and ammonia.
  3 KB (502 words) - 20:18, 6 February 2021
• Phosphorus tribromide
  *α-bromination of carboxylic acids
  6 KB (765 words) - 20:59, 2 December 2018
• Phosphorus pentabromide
  | SolubleOther = Reacts with alcohols, carboxylic acids<br>Soluble in AsCl₃, [[bromine]], liq. [[Hydrogen bromide|HBr]], ...bromide rapidly hydrolyzes in water to release hydrobromic and phorphorous acids.
  5 KB (599 words) - 20:58, 2 December 2018
• Phosphoryl bromide
  5 KB (508 words) - 15:12, 31 December 2018
• Plasticware
  ...eous solutions and diluted acids. Not employed for long term use of strong acids or organic solvents. PTFE beakers are mainly used when working with hydrofl
  7 KB (1,092 words) - 20:41, 2 October 2022
• Trifluoroacetic acid
  [[Category:Acids]] [[Category:Strong acids]]
  6 KB (682 words) - 17:27, 27 May 2023
• Ammonium dichromate
  ...tic containers, with a proper label and a hazard symbol. Keep it away from acids and open flame sources.
  5 KB (576 words) - 19:12, 9 November 2018
• Sodium oxide
  ...er = Reacts with alcohols, [[carboxylic acid]]s, esters, halogens, mineral acids<br>Insoluble in [[ether]]s, hydrocarbons
  5 KB (655 words) - 19:10, 6 February 2020
• Potassium bisulfite
  ...um bisulfite releases toxic sulfur dioxide gas, especially in contact with acids. Work in a well ventilated area or fumehood. [[Category:Acids]]
  5 KB (564 words) - 09:42, 25 June 2023
• Sodium dichromate
  ...[[sodium hydroxide]]) is added to the solution to neutralize all remaining acids and precipitate a mixture of iron and chromium hydroxides, which are then f
  5 KB (658 words) - 21:38, 23 May 2019
• Niacin
  [[Category:Carboxylic acids]] [[Category:Acids]]
  5 KB (554 words) - 21:54, 15 March 2021
• Potassium cyanide
  Potassium cyanide should be stored in closed bottles, away from any acids, in a locked cabinet with a clear hazard label on the storage bottle.
  6 KB (794 words) - 13:27, 10 July 2022
• Sodium cyanide
  | SolubleOther = Reacts with acids<br>Soluble in [[ammonia]], [[methanol]]<br>Slightly soluble in [[dimethylfo Sodium cyanide should be stored in closed bottles, away from any acids, in a locked cabinet with a clear hazard label on the storage bottle. Alkal
  10 KB (1,481 words) - 13:28, 10 July 2022
• Triethyl citrate
  Triethyl citrate should be stored in closed bottles, away from acids.
  4 KB (403 words) - 20:23, 9 January 2017
• Triethyl borate
  [[Category:Esters of inorganic acids]]
  4 KB (427 words) - 21:37, 21 January 2020
• Sodium ethoxide
  4 KB (455 words) - 18:40, 12 July 2019
• Hydroquinone
  Hydroquinone, like phenols are very weak acids and can be deprotonated.
  5 KB (540 words) - 20:05, 19 June 2019
• Ethylenediaminetetraacetic acid
  [[Category:Acids]] [[Category:Carboxylic acids]]
  5 KB (553 words) - 18:53, 5 July 2019
• Sodium dodecyl sulfate
  ...from coconut or palm kernel oil by hydrolysis (which liberates their fatty acids), followed by hydrogenation. If you don't want this route, just use dodecan
  5 KB (536 words) - 09:28, 8 September 2019
• Tartaric acid
  Tartaric acid is a crystalline colorless solid, soluble in water, acids and alcohols, but insoluble in hydrocarbons and halocarbons. [[Category:Acids]]
  7 KB (882 words) - 20:02, 14 January 2020
• Antimony(III) oxide
  Antimony(III) oxide reacts with acids to form antimony salts, which may hydrolyze if the pH is not low enough. In closed bottles, away from acids.
  4 KB (483 words) - 21:17, 15 May 2019
• Chloroplatinic acid
  [[Category:Acids]]
  4 KB (414 words) - 22:36, 28 August 2018
• Butyric acid
  ...nt of rancid butter or vomit. It is miscible in water and other carboxylic acids. [[Category:Acids]]
  4 KB (499 words) - 20:00, 7 September 2020
• Calcium propionate
  Calcium propionate reacts with strong acids to eliberate [[propionic acid]]
  4 KB (387 words) - 21:37, 27 January 2017
• Ammonium bisulfate
  [[Category:Acids]]
  3 KB (335 words) - 14:54, 28 January 2017
• Hunsdiecker reaction
  ...lk/viewthread.php?tid=66503 Halobenzenes by decarboxylation of halobenzoic acids] ...emadness.org/talk/viewthread.php?tid=83518 Hunsdiecker Reaction with Amino Acids Literature/Insight]
  1 KB (196 words) - 21:56, 15 May 2020
• Ethenone
  | SolubleOther = Reacts with carboxylic acids<br>Soluble in [[acetone]], [[benzene]], [[chloroform]], [[ethanol]]<br>Slig
  4 KB (470 words) - 22:00, 19 August 2018
• Mercury(II) oxide
  | SolubleOther = Reacts with acids<br>Insoluble in [[acetone]], alcohols, [[ammonia]], ethers, Mercury(II) oxide reacts with most acids to give mercury salts, making it the basic precursor for any mercury compou
  4 KB (528 words) - 21:26, 16 October 2022
• Silver acetate
  In closed plastic or glass containers, away from light and acids.
  4 KB (486 words) - 00:00, 30 December 2021
• Metalware
  ...r heavy objects around. It's advised not to carry corrosive reagents, like acids or halogens with it. When washing them, make sure you do not use acids, so avoid putting them in the acid bath after holding them in a base bath.
  13 KB (2,034 words) - 08:43, 5 May 2019
• Reactivation of calcinated oxides
  ...re and makes them resistant to the attack of most corrosive reagents, like acids, aqueous alkali, metal halides or halogens. Indurated oxides can be '''reac ...lk/viewthread.php?tid=21663 Very low solubility of erbium oxide in mineral acids]
  3 KB (504 words) - 19:38, 5 February 2020
• Fuming
  ===Acids===
  4 KB (615 words) - 16:25, 2 January 2023
• Ammonium dinitramide
  Ammonium dinitramide should be kept in closed plastic bottles, away from acids and anything combustible.
  7 KB (923 words) - 16:56, 19 November 2018
• Guanidine
  As a base, guanidine will react with acids to form salts. By protanating guanidine, the [[guanidinium]] ion is formed.
  7 KB (902 words) - 19:02, 27 March 2022
• Potassium tert-butoxide
  5 KB (534 words) - 20:21, 17 September 2022
• Pentanoic acid
  [[Category:Acids]] [[Category:Weak acids]]
  4 KB (451 words) - 18:29, 21 July 2019
• Titanium(IV) chloride
  [[Category:Lewis acids]]
  5 KB (622 words) - 21:01, 5 June 2021
• Redox
  *''Acids'': [[chloric acid]], [[chromic acid]]s, [[nitric acid]], peracids, [[perchl *''Acids'': [[ascorbic acid]], [[citric acid]], [[formic acid]], [[hydrogen sulfide]
  4 KB (400 words) - 15:01, 2 January 2022
• Reducer
  *''Acids'': [[ascorbic acid]], [[citric acid]], [[formic acid]], [[hydrogen sulfide]
  2 KB (181 words) - 21:43, 29 April 2018
• Potassium bitartrate
  [[Category:Acids]] [[Category:Carboxylic acids]]
  5 KB (553 words) - 20:55, 25 November 2018
• Chromium(III) chloride
  [[Category:Lewis acids]]
  5 KB (542 words) - 21:34, 7 May 2020
• Calcium cyanamide
  | SolubleOther = Reacts with acids<br>Insoluble in organic solvents
  7 KB (901 words) - 15:17, 18 November 2023
• Clemmensen reduction
  The reaction is not suitable for substances sensitive to acids. Also, [[carboxylic acid]] groups cannot be reduced by this method.
  2 KB (260 words) - 21:07, 29 July 2017
• Sodium amide
  5 KB (631 words) - 01:20, 30 August 2020
• Guanidinium nitrate
  ...trate]], the decomposition of GdnNO₃ is influenced by bases and acids.<ref>http://energetics.chm.uri.edu/system/files/Decomposition%20of%20Urea%2
  7 KB (849 words) - 17:39, 3 August 2020
• Ammonium nitrite
  | SolubleOther = Reacts with acids
  6 KB (712 words) - 20:21, 1 October 2020
• Grignard reagent
  6 KB (857 words) - 14:37, 1 April 2019
• Sodium aluminium hydride
  4 KB (488 words) - 19:20, 20 October 2019
• Guanidinium carbonate
  Guanidinium carbonate reacts with acids to release carbon dioxide and water, yielding guanidinium ions.
  4 KB (458 words) - 17:10, 23 June 2019
• Wolff–Kishner reduction
  *[http://www.sciencemadness.org/talk/viewthread.php?tid=12419 alpha-keto acids and hydrazone formation/wolff-kishner stuffs]
  3 KB (355 words) - 16:03, 20 May 2018
• Lithium hydride
  6 KB (710 words) - 09:52, 20 February 2022
• Lithium borohydride
  5 KB (558 words) - 21:28, 9 September 2023
• Sodium borohydride
  | SolubleOther = Reacts with acids, [[alcohol]]s, [[aldehyde]]s, [[carboxylic acid]]s, [[halocarbon]]s, [[keto Addition of acids speeds up the decomposing reaction. [[Boron trioxide]] has been found to be
  10 KB (1,222 words) - 19:18, 13 August 2023
• Cement
  ...generally resist the attack of oxidizers, but many corrosive reagents like acids, bases or halogens will corrode them, the speed depends on the corrosive re
  5 KB (715 words) - 15:11, 28 October 2017
• Sodium hydride
  7 KB (822 words) - 10:14, 20 February 2022
• Ketone
  3 KB (428 words) - 22:37, 10 June 2018
• Acyl halide
  Acyl halides can be prepared by reacting carboxylic acids with halogenating reagents such as cyanuric fluoride for acyl fluorides, [[
  2 KB (233 words) - 20:52, 19 May 2019
• Potassium hydrogen phthalate
  [[Category:Carboxylic acids]]
  4 KB (413 words) - 16:59, 8 July 2023
• Blanc reaction
  1 KB (214 words) - 18:52, 5 July 2019
• Benzyl chloride
  ...eaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester.
  8 KB (1,110 words) - 21:27, 7 November 2021
• Barbituric acid
  [[Category:Acids]] [[Category:Weak acids]]
  6 KB (656 words) - 18:03, 1 March 2021
• Amine
  Amines react with acids to form alkyl- or aryl-ammonium salts.
  2 KB (278 words) - 15:35, 29 August 2017
• Spatula
  ...resist most chemical reagents, though they are not compatible with strong acids, some salts (like [[copper]] salts) and halogens ([[iodine]]). It is not ad
  2 KB (385 words) - 20:54, 2 October 2022
• HI/P reduction
  3 KB (541 words) - 19:35, 19 April 2019
• Cyanuric acid
  [[Category:Acids]]
  4 KB (491 words) - 15:18, 18 November 2023
• Keck clip
  ...y excellent thermal and chemical resistance to solvents. Halogens and some acids will corrode metal kecks. Main disadvantage of metal joint clips is that th ...st high temperatures, but can be severely attacked by halogens and various acids. Biggest problem with metal clamps is that they will slowly scratch the gla
  4 KB (634 words) - 20:06, 16 November 2020
• Magnesium oxide
  ...ence of its low solubility in water. It will however react vigorously with acids, giving magnesium salts. In closed bottles, away from acids and halogens.
  5 KB (554 words) - 23:31, 20 March 2020
• Magnesium carbonate
  Magnesium carbonate reacts with acids to form magnesium salts of said acids and releasing carbon dioxide. ...onate is a white hygroscopic solid, insoluble in solvents, but reacts with acids.
  7 KB (923 words) - 18:03, 17 November 2019
• Zamak
  Zamak quickly tarnishes in air and reacts with most acids and bases, as well as halogens.
  4 KB (591 words) - 16:05, 6 October 2019
• Cork ring
  ...as it is soft and wood is not attacked by organic solvents, though strong acids and bases will slowly damage it. It can also resist temperatures up until 2
  3 KB (517 words) - 21:22, 8 June 2023
• Evaporating dish
  The glazing covering the inside of the dish resists the attack of many acids, but will be attacked by alkali at high temperatures.
  2 KB (252 words) - 22:45, 24 January 2019
• Alkaloid
  ...es. They are nearly universally bitter in taste. Alkaloids form salts with acids; these salts tend to be soluble in water, while freebase alkaloids are spar
  4 KB (589 words) - 18:29, 22 July 2023
• Wood's metal
  Wood's metal has low reactivity with many acids, such as [[hydrochloric acid]], but is rapidly corroded by [[nitric acid]].
  2 KB (349 words) - 17:10, 10 December 2019
• Nitration
  4 KB (524 words) - 16:18, 14 April 2020
• Benzoquinone
  ...aturated ketones. 1,4-Benzoquinone is sensitive toward both strong mineral acids and alkali, which cause condensation and decomposition of the compound.
  5 KB (539 words) - 20:21, 14 August 2020
• Lab tips & tricks
  ...s method however is impractical for large bottles, but except for volatile acids you won't usually work with large quantities of hazardous chemicals.
  13 KB (2,315 words) - 17:30, 26 September 2022
• Drying rack
  ...corrosion if the protective coating is damaged or breaks down and water or acids enter contact with the metal. This is a problem mostly for old drying racks
  2 KB (364 words) - 19:39, 15 July 2019
• Surgical instrument
  ...y, while displaying good chemical resistance to most reagents, except some acids, halogens, etc. Surgical items made of metal should not be exposed to acids or halogens.
  5 KB (721 words) - 17:35, 22 June 2019
• Amino acid
  '''Amino acids''' are organic compounds containing [[amine]] (-NH₂) and [[carbo ...(N). Other elements, such as [[sulfur]] (S) are encountered in some amino acids, as well other organic groups, such as aromatic rings.
  2 KB (200 words) - 21:46, 9 October 2019
• Caffeine
  Caffeine reacts with acids to give salts of caffeine. Reaction with [[citric acid]] will give caffeine
  7 KB (810 words) - 19:20, 30 December 2023
• Glutamic acid
  [[Category:Carboxylic acids]] [[Category:Amino acids]]
  5 KB (602 words) - 18:23, 3 August 2020
• Crucible tongs
  Keep the crucible tongs away from haloacids and halogens, as well as strong acids.
  1 KB (148 words) - 21:51, 10 June 2021
• Odor
  ...th of an odor is given by the sensitivity of the olfactory nerve. Volatile acids and halogens can also be detected at relative low concentrations, while som
  3 KB (421 words) - 15:46, 5 January 2020
• Glycine
  ...H₂-CH₂-COOH'''. It is one of the proteinogenic amino acids. ...es a proton with a pKa of about 9.6 and can therefore form salts both with acids and bases.
  5 KB (559 words) - 20:19, 5 January 2020
• Oleum
  [[Category:Acids]] [[Category:Strong acids]]
  5 KB (725 words) - 22:50, 20 January 2020
• Peroxydisulfuric acid
  [[Category:Acids]] [[Category:Strong acids]]
  5 KB (570 words) - 00:22, 29 March 2020
• Sodium sulfide
  Sodium sulfide reacts with acids to release [[hydrogen sulfide]]. ...m hydroxide, sodium sulfide is strongly alkaline and can cause skin burns. Acids react with it to rapidly produce hydrogen sulfide, which is highly toxic.
  5 KB (548 words) - 19:59, 24 October 2023
• Sodium fluoride
  Avoid contact with strong acids, as it will release hydrofluoric acid.
  5 KB (553 words) - 20:30, 16 October 2022
• Copper(I) oxide
  | SolubleOther = Reacts with acids, aq. [[ammonia|NH₃]]<br>Insoluble in alcohols, ethers, halocarbo
  5 KB (541 words) - 08:22, 5 August 2021
• Dehydration reaction
  2 KB (202 words) - 18:43, 19 July 2019
• Sodium chlorite
  | SolubleOther = Reacts with acids<br>Slightly soluble in [[ethanol]], [[methanol]] Sodium chlorite reacts with acids and elemental chlorine to yield chlorine dioxide.
  5 KB (612 words) - 22:41, 13 February 2021
• Barium peroxide
  | SolubleOther = Reacts with acids<br>Insoluble in hydrocarbons
  5 KB (530 words) - 17:04, 13 February 2022
• Sodium chromate
  ...[[sodium hydroxide]]) is added to the solution to neutralize all remaining acids and precipitate a mixture of iron and chromium hydroxides, which are then f
  6 KB (735 words) - 21:39, 23 May 2019
• Organic acid anhydride
  Acid anhydrides react with halogen acids, reaction which yields equal amounts of the acylated product and the carbox Laboratory routes rely on the dehydration of the corresponding acids or their salts. A variety of methods have been developed, because anhydride
  5 KB (861 words) - 19:09, 12 February 2024
• Chlorite
  Chlorite salts, like sodium chlorite reacts with acids and elemental [[chlorine]] to yield [[chlorine dioxide]]. Chlorites are powerful oxidizers. Avoid contact with acids, as the reaction will release toxic chlorine dioxide.
  2 KB (277 words) - 22:13, 16 September 2020
• Erbium(III) oxide
  | SolubleOther = Reacts with acids<br>Insoluble in solvents ...de]] from the atmosphere, forming erbium(III) carbonate. It can react with acids to form the corresponding erbium(III) salts. This makes it a good precursor
  4 KB (392 words) - 22:18, 8 November 2018
• Calcium chromate
  | SolubleOther = Reacts with strong acids<br>Practically insoluble in [[alcohol]]
  4 KB (493 words) - 15:12, 10 January 2019
• Fluorosulfuric acid
  ...'''sulfurofluoridic acid''' is one of the strongest commercially available acids, more specifically a superacid. It has the chemical formula '''HFSO<sub>3</
  5 KB (565 words) - 19:10, 8 November 2023
• Peracetic acid
  | SolubleOther = Miscible with alcohols, carboxylic acids<br>Soluble in ether [[Category:Acids]]
  5 KB (621 words) - 16:36, 28 August 2018
• Dimethyl dioxane
  ...use acid, like in the case of dioxane, as dimethyldioxane is sensitive to acids. Instead, a base like [[sodium hydroxide|sodium]] or [[potassium hydroxide]
  7 KB (865 words) - 16:40, 4 September 2019
• Strontium nitrate
  ...rate should be stored in plastic or glass containers or bottles, away from acids and any flammable materials.
  5 KB (648 words) - 17:44, 12 September 2022
• Lead(IV) oxide
  | SolubleOther = Reacts with mineral acids<br>Soluble in [[acetic acid]], alkalis<br>Insoluble in [[alcohol]]s, [[keto ...he instability of its Pb⁴⁺ cation, lead dioxide reacts with hot acids, converting to the more stable Pb²⁺ state and liberating oxygen,
  11 KB (1,482 words) - 20:24, 23 October 2022
• Ricinoleic acid
  [[Category:Acids]] [[Category:Weak acids]]
  5 KB (563 words) - 09:16, 25 June 2023
• Barium oxide
  | SolubleOther = Reacts with alcohols, acids, [[bromine]], [[phenol]]<br>Insoluble in liq. [[ammonia]], organic solvents Reaction with acids yields barium salts.
  4 KB (445 words) - 20:32, 13 March 2024
• Quinine
  Quinine reacts with acids forming water soluble salts.
  5 KB (640 words) - 18:36, 5 March 2024
• Sulfamic acid
  [[Category:Acids]] [[Category:Strong acids]]
  7 KB (910 words) - 12:58, 18 November 2023
• Glycolic acid
  ...Cu2+ which are significantly stronger than complexes with other carboxylic acids. This indicates that the hydroxyl group is involved in complex formation, p *Make monohaloacetic acids
  6 KB (661 words) - 21:33, 22 July 2020
• Thioglycolic acid
  [[Category:Acids]] [[Category:Mid-strength acids]]
  5 KB (535 words) - 18:52, 22 May 2019
• Alcohol catalyzed alkali metal production
  *Carboxylic acids: none work
  18 KB (2,804 words) - 20:34, 17 September 2022
• Sorbic acid
  [[Category:Acids]] [[Category:Weak acids]]
  4 KB (460 words) - 16:39, 31 December 2021
• PH
  ...belief, the pH value can be less than 0 or greater than 14 for very strong acids and bases respectively.
  2 KB (310 words) - 19:24, 23 October 2022
• Rubidium hydroxide
  | SolubleOther = Reacts with acids<br>Soluble in [[ethanol]], [[methanol]]<br>Insoluble in anh. [[ammonia]], [ Rubidium hydroxide should be kept in air-tight containers, away from acids.
  5 KB (547 words) - 23:02, 26 April 2019
• Primary alcohol
  Primary alcohols can be oxidized to aldehydes or carboxylic acids.
  427 B (50 words) - 20:55, 22 March 2019
• Carbide
  ...ransition metal carbides resist hydrolysis, but will be slowly attacked by acids.
  3 KB (466 words) - 17:34, 3 October 2021
• Oxalyl chloride
  4 KB (503 words) - 21:47, 11 October 2022
• Buffering agent
  ...the function of a buffering agent is to prevent a rapid change in pH when acids or bases are added to the solution. Buffering agents have variable properti
  549 B (86 words) - 23:57, 24 March 2019
• Chloroacetic acid
  ...pure product, which can be important since mono-, di-, and trichloroacetic acids are difficult to separate by distillation. [[Category:Acids]]
  7 KB (843 words) - 19:47, 15 September 2022
• Bromoacetic acid
  [[Category:Acids]] [[Category:Mid-strength acids]]
  4 KB (433 words) - 19:30, 18 June 2019
• Iodoacetic acid
  ...acid is corrosive and highly poisonous. As the toxicity of monohaloacetic acids increases with halogen size, iodoacetic acid is more toxic than [[bromoacet [[Category:Acids]]
  4 KB (371 words) - 19:30, 18 June 2019
• Aminoguanidine
  | SolubleOther = Reacts with acids
  5 KB (576 words) - 20:00, 12 March 2021
• Ash
  Since ash is strongly alkaline, it will react with acids, releasing [[carbon dioxide]].
  3 KB (479 words) - 12:06, 2 November 2021
• Resorcinol
  ...with [[sodium nitrite]], a water-soluble blue dye, which is turned red by acids, and is used as an [[PH indicator|indicator]], under the name of lacmoid. [[Category:Weak acids]]
  5 KB (507 words) - 19:52, 25 October 2020
• Guanidinium bicarbonate
  Guanidinium bicarbonate reacts with acids to form guanidinium salts and releasing [[carbon dioxide]].
  3 KB (346 words) - 22:03, 24 October 2022
• Nitro compound
  *Oxidation of oximes or primary amines with peroxycarboxylic acids or [[Dimethyldioxirane|DMDO]]. *Decarboxylation of α-nitro carboxylic acids formed from nitriles and ethyl nitrate.
  6 KB (839 words) - 21:28, 26 October 2020
• Hypochlorous acid
  When acids are added to aqueous salts of hypochlorous acid (such as sodium hypochlorit [[Category:Acids]]
  5 KB (628 words) - 19:54, 21 April 2019
• Barium permanganate
  ...rosive and a strong oxidizer. Avoid contact with combustible materials and acids.
  4 KB (401 words) - 18:57, 12 March 2023
• Wood
  ...burn if ignited in an oxygen-rich environment, like air. Wood reacts with acids.
  3 KB (404 words) - 22:22, 13 February 2021
• Paper
  Paper reacts with acids differently: reaction with conc. [[sulfuric acid]] will cause it to turn bl
  2 KB (273 words) - 10:46, 2 April 2020
• Regulatory quirks
  ...as in "compounds that may generate poisonous gases in contact with water, acids or bases", which can also refer to other non-phosphide compounds. ...dumping certain harmless lab-grade reagents, like acetic, citric, tartaric acids and their salts, sodium hydroxide, various alcohols and esters, that not on
  44 KB (6,991 words) - 19:37, 8 January 2024
• Butylated hydroxytoluene
  [[Category:Weak acids]]
  5 KB (560 words) - 17:13, 30 November 2022
• Eucalyptol
  Eucalyptol forms crystalline [[adduct]]s with hydrohalic acids, o-cresol, [[resorcinol]] and [[phosphoric acid]]. Formation of these adduc
  4 KB (452 words) - 20:29, 15 September 2022
• Kojic acid
  .../www.sciencemadness.org/whisper/viewthread.php?tid=54463 Producing Organic Acids with Microorganisms] [[Category:Acids]]
  6 KB (719 words) - 23:23, 1 March 2024
• Lactic acid
  [[Category:Acids]] [[Category:Mid-strength acids]]
  5 KB (588 words) - 21:39, 13 June 2020
• Chlorous acid
  Both resulting acids are also unstable in concentrated form, and will too further decompose to [ [[Category:Acids]]
  4 KB (453 words) - 16:36, 17 June 2019
• Fluoroacetic acid
  [[Category:Acids]] [[Category:Mid-strength acids]]
  5 KB (570 words) - 17:26, 27 May 2023
• Difluoroacetic acid
  [[Category:Acids]] [[Category:Mid-strength acids]]
  4 KB (366 words) - 17:27, 27 May 2023
• Dichloroacetic acid
  ...d]] in the presence of UV light will yield mono-, di- and tri-chloroacetic acids. Separating the components via fractional distillation is difficult but doa [[Category:Acids]]
  4 KB (485 words) - 20:52, 2 February 2020
• Trichloroacetic acid
  [[Category:Acids]] [[Category:Strong acids]]
  5 KB (607 words) - 19:45, 27 July 2022
• Ytterbium(III) oxide
  | SolubleOther = Reacts with acids<br>Insoluble in organic solvents Ytterbium(III) oxide reacts with acids forming salts.
  3 KB (309 words) - 16:36, 23 October 2023
• Yttrium(III) oxide
  | SolubleOther = Reacts with acids
  4 KB (410 words) - 16:12, 22 June 2019
• Borderline chemical compound
  Perhalocarboxylic acids, like [[trifluoroacetic acid]] are sometimes classified as inorganic, thoug
  3 KB (488 words) - 16:25, 2 January 2020
• Cerium(IV) oxide
  | SolubleOther = Reacts with acids Cerium(IV) oxide is a white solid, odorless which reacts with acids.
  3 KB (344 words) - 17:05, 23 June 2019
• Friedel-Crafts reaction
  ...wever, because the product ketone forms a rather stable complex with Lewis acids such as AlCl3, a stoichiometric amount or more of the "catalyst" must gener
  2 KB (230 words) - 21:46, 11 October 2022
• Soap
  Since they are salts of fatty acids, soaps have the general formula (RCO₂⁻)₂
  2 KB (345 words) - 12:47, 23 December 2021
• Triphenylphosphine
  Triphenylphosphine is a weak base, but does form stable salts with strong acids such as HCl and HBr.
  4 KB (456 words) - 14:18, 6 October 2019
• Trimethylphosphine
  Trimethylphosphine is a weak [[base]], but does form stable salts with strong acids.
  5 KB (594 words) - 22:30, 21 January 2020
• Ferulic acid
  ...ions in popcorn and bamboo shoots. It is a major metabolite of chlorogenic acids in humans along with caffeic and isoferulic acid. [[Category:Acids]]
  5 KB (539 words) - 18:37, 19 October 2019
• Thiourea
  | SolubleOther = Reacts with acids<br>Soluble in [[ethanol]], [[methanol]]<br>Almost insoluble in [[diethyl et
  5 KB (540 words) - 20:40, 15 September 2022
• Thiourea dioxide
  [[Category:Acids]] [[Category:Sulfinic acids]]
  4 KB (447 words) - 17:55, 13 May 2020
• Resin
  ...e, and delta-cadinene. Some resins also contain a high proportion of resin acids. Rosins on the other hand are less volatile and contain many diterpenes.<re
  2 KB (321 words) - 23:44, 2 January 2020
• Propionaldehyde
  Propanal will polymerize in presence of strong acids acids or bases. Can also occur in contact with methyl methacrylate.
  5 KB (511 words) - 21:21, 15 September 2022
• Hydroxylammonium chloride
  *Preparation of oximes and hydroxamic acids
  9 KB (1,090 words) - 09:47, 25 June 2023
• Hydroxylammonium sulfate
  *Preparation of oximes and hydroxamic acids
  4 KB (499 words) - 19:50, 8 January 2020
• Anthranilic acid
  [[Category:Carboxylic acids]] [[Category:Anthranilic acids]]
  5 KB (521 words) - 17:43, 30 June 2020
• Barium azide
  | SolubleOther = Reacts with acids<br>Insoluble in [[acetone]], [[diethyl ether]], [[carbon tetrachloride|CCl<
  5 KB (604 words) - 22:24, 13 February 2021
• Aluminium phosphide
  | SolubleOther = Reacts with acids<br>Insoluble in organic solvents ...ich an unpleasant garlic-like odor, highly toxic. It reacts with water and acids, and it is not soluble in organic solvents.
  5 KB (633 words) - 10:28, 9 February 2020
• Ethyl nitrate
  ...cid]], fuming nitric acid or a mixture of concentrated sulfuric and nitric acids, in the presence of [[urea]].<ref>https://www.prepchem.com/synthesis-of-eth
  7 KB (870 words) - 10:47, 10 July 2022
• Triethanolamine
  | SolubleOther = Reacts with acids<br>Miscible with [[acetone]], [[chloroform]], [[ethanol]], [[isopropanol]], Triethanolamine is a strong base and readily reacts with acids. In the presence of water, it will readily absorb carbon dioxide from air t
  5 KB (580 words) - 20:34, 5 December 2020
• Potassium nitrite
  In closed bottles, in a dry place, away from any acids.
  7 KB (890 words) - 20:09, 24 October 2023
• Lithium nitrate
  In closed glass or plastic bottles, away from acids and flammable materials.
  5 KB (555 words) - 11:27, 29 February 2020
• Boron nitride
  Boron nitride is insoluble in most common acids, but is soluble in alkaline molten salts and nitrides, such as [[Lithium hy
  6 KB (812 words) - 20:57, 23 October 2022
• Magnesium diboride
  Magnesium diboride reacts with dilute acids to release hydrogen and a small amount of boranes, while reaction with wate
  5 KB (516 words) - 16:18, 2 January 2022
• Fluoroboric acid
  [[Category:Acids]] [[Category:Strong acids]]
  5 KB (593 words) - 23:04, 8 August 2020
• Lead(II) chloride
  ...[hydrochloric acid]], aq. [[ammonia]]<br>Insoluble in alcohols, carboxylic acids, hydrocarbons
  5 KB (629 words) - 00:22, 26 August 2020
• Hypophosphorous acid
  [[Category:Acids]] [[Category:Mineral acids]]
  6 KB (673 words) - 21:59, 14 June 2020
• Trimethyl phosphate
  [[Category:Esters of inorganic acids]]
  4 KB (491 words) - 11:35, 28 December 2020
• Ferroin
  In closed dark amber bottles, away from oxidizing agents and acids.
  4 KB (484 words) - 19:38, 31 March 2020
• Beeswax
  ...of the genus Apis. Chemically, beeswax consists mainly of esters of fatty acids and various long-chain alcohols. ...rage, unhydrolyzed beeswax contains esters (71%), hydrocarbons (15%), free acids (8%) and other compounds (~6%).<ref>https://link.springer.com/article/10.10
  3 KB (473 words) - 16:14, 17 January 2021
• Vegetable oil
  ...s cooking oil and are generally edible. Triglycerides of less common fatty acids, such as [[ricinoleic acid]] are not suitable for consumption and are inste ...as peroxides and hydroperoxides, plant oils rich in polyunsaturated fatty acids have a limited shelf-life.
  5 KB (701 words) - 18:56, 19 April 2020
• Rubber
  ...specialty materials. It also resists the chemical attack of many solvents, acids and oxidizers, though halogens and nitric acid/nitrogen dioxide will corrod
  5 KB (699 words) - 20:24, 2 October 2022
• Phenethyl alcohol
  ...HF]].<ref>Kanth JV, Periasamy M (1991). "Selective Reduction of Carboxylic Acids into Alcohols Using NaBH and I2". Journal of Organic Chemistry. 56: 5964–
  6 KB (682 words) - 21:25, 1 October 2023
• Styphnic acid
  [[Category:Acids]]
  6 KB (671 words) - 19:33, 16 May 2023
• Ether cleavage
  ...[[ether]]s. The most common reagents used in ether cleavage are hydrohalic acids and certain organolithium compounds. ...[hydrofluoric acid]] to cleave ethers in protic media. Usage of hydrohalic acids takes advantage of the fact that these agents are able to protonate the eth
  3 KB (518 words) - 16:20, 6 June 2020
• Benzylamine
  Benzylamine reacts with acids forming salts.
  5 KB (561 words) - 11:40, 20 August 2020
• Glycoluril
  Nitration of glycoluril with a mixture of conc. nitric and sulfuric acids yields [[tetranitroglycoluril]] (TNGU), a potent explosive.
  4 KB (487 words) - 16:09, 12 October 2020
• Cadmium oxide
  | SolubleOther = Reacts with acids<br>Slowly soluble in ammonium salts<br>Insoluble in alkalis, organic solven CdO is a basic oxide and is thus attacked by aqueous acids to give solutions of [Cd(H₂O)₆]²⁺. Upon tr
  4 KB (520 words) - 22:09, 25 August 2020
• Nickel(II) perchlorate
  Nickel(II) perchlorate is a powerful oxidizing agent. In contact with strong acids, it will ignite organic material on contact.
  5 KB (543 words) - 20:43, 16 November 2020
• Nitrosylsulfuric acid
  [[Category:Acids]] [[Category:Mineral acids]]
  6 KB (736 words) - 19:21, 22 March 2021
• Tetranitroglycoluril
  6 KB (680 words) - 21:39, 26 October 2020
• Trinitrophloroglucinol
  [[Category:Acids]]
  5 KB (559 words) - 19:47, 25 October 2020
• Aminoguanidinium bicarbonate
  Aminoguanidinium bicarbonate will react with acids to yield their respective salts.
  7 KB (851 words) - 10:04, 7 May 2021
• Tetrabutyltin
  TBT reacts easily with halogens, hydrogen halides and most acids.
  5 KB (602 words) - 21:02, 1 November 2020
• Borazine
  | SolubleOther = Reacts with acids
  6 KB (810 words) - 22:09, 6 November 2020
• Phloroglucinol
  [[Category:Weak acids]]
  5 KB (542 words) - 00:10, 15 November 2020
• Ethylamine
  | SolubleOther = Reacts with acids<br>Miscible with [[acetone]], [[benzene]], [[diethyl ether]], [[ethanol]], Ethylamine reacts with acids to form their respective salts.
  7 KB (882 words) - 21:56, 15 November 2020
• Zinc perchlorate
  Zinc perchlorate is a powerful oxidizing agent. In contact with strong acids, it will ignite organic material on contact.
  6 KB (650 words) - 22:29, 15 August 2022
• Dimethylzinc
  ...ubleOther = Reacts with alcohols, bases, carboxylic acids, esters, mineral acids<br>Miscible with [[benzene]], [[diethyl ether]], [[hexane]], [[toluene]], [
  7 KB (843 words) - 22:43, 17 November 2020
• Pyruvic acid
  '''Pyruvic acid''' is the simplest of the keto acids, as well as alpha-keto acids, which are compounds with a carboxylic acid and a ketone functional group. ...d back to carbohydrates (such as glucose) via gluconeogenesis, or to fatty acids through a reaction with acetyl-CoA.
  6 KB (709 words) - 21:06, 15 September 2022
• Diethanolamine
  Diethanolamine is a base, and will react with acids to form salts.
  5 KB (544 words) - 23:22, 5 December 2020
• Succinonitrile
  ...dness.org/whisper/viewthread.php?tid=29248 Useful intermediates from amino-acids and related compounds]
  5 KB (509 words) - 12:12, 29 December 2020
• Phenylacetic acid
  [[Category:Acids]] [[Category:Weak acids]]
  8 KB (1,054 words) - 15:20, 17 August 2022
• Ascaridole
  ...e and prone to explosion when heated above 130 °C or treated with organic acids. This however only happens for large amounts and the deflagration is not ve
  6 KB (660 words) - 20:03, 29 December 2020
• Periodic acid
  [[Category:Acids]] [[Category:Mineral acids]]
  6 KB (732 words) - 18:19, 15 March 2022
• Violuric acid
  [[Category:Acids]] [[Category:Weak acids]]
  4 KB (487 words) - 15:30, 25 May 2021
• Calcium bicarbonate
  | SolubleOther = Reacts with acids Solutions of calcium carbonate react with acids forming calcium salts of said acids and releasing carbon dioxide.
  4 KB (498 words) - 19:48, 12 March 2021
• Purple acid
  *Similarly adducts of NO with strong Lewis acids are known, such as with HCl, BF₃ and SO₃. [[Category:Acids]]
  9 KB (1,331 words) - 13:07, 28 January 2023
• Iodic acid
  ...loric acid]] and [[bromic acid]], iodic acid is one of the most stable oxo-acids of the halogens. [[Category:Acids]]
  8 KB (1,012 words) - 21:27, 24 May 2021
• Lithium hypochlorite
  | SolubleOther = Reacts with acids, amines Lithium hypochlorite reacts with acids to give [[hypochlorous acid]], which decomposes releasing [[chlorine]].
  4 KB (341 words) - 11:23, 26 November 2022
• Bromous acid
  [[Category:Acids]] [[Category:Mineral acids]]
  5 KB (644 words) - 21:59, 10 July 2022
• Barium chromate
  | SolubleOther = Soluble in strong acids ...powdered solid, practically insoluble in water, but more soluble in conc. acids.
  5 KB (508 words) - 14:44, 5 June 2021
• Malonic acid
  [[Category:Acids]] [[Category:Mid-strength acids]]
  5 KB (526 words) - 21:53, 17 September 2022
• 2-Mercaptoethanol
  [[Category:Acids]] [[Category:Weak acids]]
  4 KB (462 words) - 20:47, 14 November 2021
• Magnalium
  ...ids and bases, while Mg-rich magnalium alloys are more susceptible to most acids, as well as water. The latter is also much more flammable. Neither types re In closed airtight bottles, away from moisture, acids and fire.
  3 KB (459 words) - 17:39, 25 November 2021
• Cyclam
  | SolubleOther = Reacts with acids In closed bottles, away from acids.
  3 KB (364 words) - 13:09, 31 December 2021
• Triaminoguanidine
  Triaminoguanidine will react with acids to form salts. In closed airtight bottles, away from acids.
  5 KB (526 words) - 22:23, 25 November 2021
• Aluminium iodide
  [[Category:Lewis acids]]
  6 KB (800 words) - 13:19, 18 November 2023
• Sodium bismuthate
  | SolubleOther = Reacts with acids<br>Insoluble in most solvents ...te can perform oxidative 1,2-cleavage on glycols, ketols and alpha hydroxy acids with no further oxidation of the (possible) aldehyde products. These cleava
  7 KB (821 words) - 22:03, 29 December 2021
• Potassium bismuthate
  In closed plastic or glass bottles, away from moisture and acids.
  6 KB (701 words) - 22:02, 29 December 2021
• Lithium azide
  | SolubleOther = Reacts with acids<br>Soluble in [[ethanol]], [[hydrazine]], [[methanol]]<br>Insoluble in [[di
  5 KB (626 words) - 15:46, 2 January 2022