Hydrochloric acid
7647-01-0 · 4-D Bowl Sanitizer · Acid, Hydrochloric · Acid, Muriatic · Acide chlorhydrique · Acido clorhidrico · Acido cloridrico · Acidum hydrochloricum · Acidum Muriaticum · Anhydrous hydrochloric acid · Anhydrous hydrogen chloride · Aqueous hydrogen chloride · Baume hcl · Bowl Cleaner · Caswell No. 486 · Chloorwaterstof · chlorane · chlorhydric acid · Chloride, Hydrogen · Chlorohydric acid · Chlorowodor · chlorure d'hydrogene · Chlorure d'hydrogene anhydre · Chloruro de hidrogeno · Chlorwasserstoff · cloruro de hidrogeno · Cloruro de hidrogeno anhidro · Deuterium-chloride · E 507 · Emulsion Bowl Cleaner · Enplate po 236 · EPA Pesticide Chemical Code 045901 · Funoran · HCl · HEMMORHOIDS · HSDB 545 · Hydrochloric acid · Hydrochloric acid gas · Hydrochloric acid, ACS reagent, 37% · Hydrochloric acid, anhydrous · hydrochloricacid · Hydrogen chloride · Hydrogen chloride (acid) · Hydrogen chloride (gas only) · Hydrogen chloride (HCl) · Hydrogen Chloride - Methanol Reagent · Hydrogenchlorid · Hygeia Creme Magic Bowl Cleaner · Icon etch · INS NO.507 · INS-507 · Marine acid · mono hydrochloride · monohydrochloride · Muriatic acid · Muriaticum acidum · Percleen Bowl and Urinal Cleaner · UN 1050 (anhydrous) · UN 2186 (refrigerated liquefied gas) · White Emulsion Bowl Cleaner · E507 · 507 · hydrogen chloride · Hydrochloric acid · Acid clorhidric · Acide chlorhydrique · Acido cloridrico · Aċidu idrokloriku · Hydrochloric acid · Kloridna kiselina · klorovodikova kislina · KWAS CHLOROWODOROWY · Kwas chlorowodorowy (kwas solny) · Kyselina chlorovodíková · Saltsyra · Saltsyre · Salzsäure · SOLNA KISELINA · Soolhape · Suolahappo · Sósav · SĀLSKĀBE · Sālsskābe · Vandenilio chlorido rūgštis · Zoutzuur · Ácido clorhídrico · Υδροχλωρικό οξύ · Солна киселинаE number E507INS 507CAS 7647-01-0
Listed as an acidity regulator by Canada, Codex and the US.
Listed as acidity regulators (CA, US, Codex) · formulation aids (US) · starch-modifying agents (CA)
- Canada: Acidity regulator — Health Canada, List of Permitted Acidity Regulators and Acid-Reacting Materials (List 10)
- United States: pH control agent — FDA, Substances Added to Food: HYDROCHLORIC ACID
- Codex Alimentarius: Acidity regulator — CXS 192-1995 Table One, INS 507
- United States: Formulation aid — FDA, Substances Added to Food: HYDROCHLORIC ACID
- Canada: Starch-modifying agent — Health Canada, List of Permitted Starch-Modifying Agents (List 13)

Hydrochloric acid is used as a processing aid and acidity regulator, chiefly to hydrolyse proteins and starches and to adjust pH during manufacture. It is generally neutralised before the food is finished.
Where it is and isn’t permitted
| Jurisdiction | Status | Scope and limits | Citation |
|---|---|---|---|
| Australia and New Zealand | Permitted, with conditions | 54 food categories no numerical limit (good manufacturing practice) Show every food category
| Food Standards Code, Schedule 15, S15—5and 53 further provisionsretrieved 2026-10-17 |
| Canada | Permitted | no numerical limit (good manufacturing practice) 5 permitted uses Show every permitted use
| Health Canadaand 4 further provisionsretrieved 2026-10-17 |
| European Union | Permitted, with conditions | 71 food categories Show every food category
| Regulation (EC) No 1333/2008and 70 further provisionsretrieved 2026-10-18 |
| Great Britain | Permitted, with conditions | 69 food categories Show every food category
| Assimilated Regulation (EC) No 1333/2008and 68 further provisionsretrieved 2026-10-18 |
| Japan | Permitted, with conditions | Designated additive: Appended Table 1, item 90, 塩酸 (“Hydrochloric Acid” in the unofficial English translation). …Designated additive: Appended Table 1, item 90, 塩酸 (“Hydrochloric Acid” in the unofficial English translation). Standards for use — Specifications and Standards for Foods, Food Additives, etc. (MHW Notification No. 370 of 1959), Part II (Food Additives), F (Standards for use), entry 塩酸: (1) [must be removed or broken down before the food is finished] “塩酸は、最終食品の完成前に中和し、又は除去しなければならない。” The Japanese is the standard as published. There is no official English translation of the Notification; the English in square brackets is this site’s description of what each sentence does, not a translation of the foods or the levels. Compositional specifications for this additive, in the same Notification, are not imported and are not shown here; nor are the general rules in F 添加物一般, which apply to every additive. | Regulations for Enforcement of the Food Sanitation Act (MHW Ordinance No. 23 of 1948), Appended Table 1retrieved 2026-10-18 |
| South Korea | Permitted, with conditions | Designated food additive: Standards and Specifications for Food Additives, Part III, 2. …Designated food additive: Standards and Specifications for Food Additives, Part III, 2. 가공보조제 (processing aids), 염산 (“Hydrochloric Acid”, the English the Code prints beside it). Main use (주용도) of 염산: 제조용제. Standard for use (사용기준) of 염산: (1) [must be neutralised or removed before the final food is complete] “염산은 최종식품 완성 전에 중화 또는 제거하여야 한다.” The Korean is the standard as published. There is no official English translation of the current Code (the English version on MFDS’s website is the 2020 edition and has no legal effect); the English in square brackets is this site’s description of what each sentence does, not a translation of the foods or the levels. Compositional specifications (Part IV) are not imported, nor are the general standards in Part II, which apply to every additive. | Standards and Specifications for Food Additives (식품첨가물의 기준 및 규격), MFDS Notification, Part III (Standards for use, by item)retrieved 2026-10-18 |
| United States | Permitted | 21 CFR 182.1057retrieved 2026-10-17 | |
| Codex Alimentarius | Permitted, with conditions | 1 food category no numerical limit (good manufacturing practice) Note XS73 Excluding products conforming to the Standard for Canned Baby Foods (CODEX STAN 73-1981). | CXS 192-1995 Table Three, INS 507and 1 further provisionretrieved 2026-09-07 |
How much is permitted
A listing usually limits the quantity as well as the food. Only one of the forms that takes is a figure: quantum satis and good manufacturing practice permit the amount the technological effect requires and no more, which is a limit rather than the absence of one. Figures below are the range across every food category this page is listed in, and categories differ between regulators — see how much is permitted.
| Australia and New Zealand | — | 54 GMP |
|---|---|---|
| Canada | — | 5 GMP |
| European Union | — | 46 several limits, 3 quantum satis, 22 no quantity stated |
| Great Britain | — | 69 quantum satis |
| Japan | — | 1 no quantity stated |
| South Korea | — | 1 no quantity stated |
| United States | — | 1 no quantity stated |
| Codex Alimentarius | — | 2 GMP |
No regulator sets a figure for Hydrochloric acid. That is not an absence of control: where the listing says quantum satis or good manufacturing practice, the quantity is limited to what the effect requires.
What it is made from
Produced industrially by combining hydrogen and chlorine, or as a by-product of organic chlorination. It is the same acid the stomach produces.
- Vegan
- Vegetarian
Compare other additives on the dietary indexes.
- CAS registry number
- 7647-01-0
- InChIKey
- VEXZGXHMUGYJMC-UHFFFAOYSA-N
- PubChem
- CID 313
The two specifications, compared
The European Union sets identity and purity by regulation; JECFA publishes its own through FAO, advisory until a country adopts it. Both documents are below in full. These are the parameters each puts a number on.
| Parameter | European Union | JECFA |
|---|---|---|
| Assay | no less than 35 % | no less than 97 % |
| Lead | no more than 1 mg/kg | no more than 1 mg/kg |
| Arsenic | no more than 1 mg/kg | — |
| Mercury | no more than 1 mg/kg | — |
One parameter differs between the two documents. A difference is not a disagreement about safety: the two are revised on their own cycles, and an assay or a drying loss can be measured against a different preparation of the substance, which is why only the contaminant ceilings are marked. Within the EU the EU's figure is the one that binds.
How the EU defines it
The legal specification an additive must meet to be sold as this E number in the EU — what it is, how it may be made, and the purity it must reach. From Commission Regulation (EU) No 231/2012.
E 507 Hydrochloric acid
Synonyms: Hydrogen chloride; Muriatic acid
Assay, identification and purity criteria
Description and assay
- Einecs
- 231-595-7
- Chemical name
- Hydrochloric acid
- Chemical formula
- HCl
- Molecular weight
- 36,46
- Assay
- Hydrochloric acid is commercially available in varying concentrations. Concentrated hydrochloric acid contains not less than 35,0 % HCl
- Description
- Clear, colourless or slightly yellowish, corrosive liquid having a pungent odour
Identification
- Test for acid
- Passes test
- Test for chloride
- Passes test
- Solubility
- Soluble in water and in ethanol
Purity criteria
- Total organic compounds
- Total organic compounds (non-fluorine containing): not more than 5 mg/kg Benzene: not more than 0,05 mg/kg Fluorinated compounds (total): not more than 25 mg/kg
- Non-volatile matter
- Not more than 0,5 %
- Reducing substances
- Not more than 70 mg/kg (as SO₂)
- Oxidising substances
- Not more than 30 mg/kg (as Cl₂)
- Sulphate
- Not more than 0,5 %
- Iron
- Not more than 5 mg/kg
- Arsenic
- Not more than 1 mg/kg
- Lead
- Not more than 1 mg/kg
- Mercury
- Not more than 1 mg/kg
How JECFA defines it
The international specification for identity and purity, prepared by the Joint FAO/WHO Expert Committee on Food Additives and published by FAO. It is a different document from any above, written by a different body and revised on its own cycle; it is advisory, and a country adopts it or does not.
INS 507 Hydrochloric Acid
Synonyms: Muriatic acid, INS No. 507 Muriatic acid
Assay, identification and purity criteria
Description and assay
- Specification history
- Prepared at the 46th JECFA (1996), published in FNP 52 Add 4 (1996) superseding specifications prepared at the 20th JECFA (1976), published in FNS 1B (1977) and in FNP 52 (1992). Metals and arsenic specifications revised at the 59th JECFA (2002). An ADI not limited' was established at the 9th JECFA (1965)
- Chemical names
- Hydrochloric acid
- C.A.S. number
- 7647-01-0
- Chemical formula
- HCl
- Formula weight
- 36.46
- Assay
- Not less than 97.0% and not more than 103.0% of the labelled amount
- DESCRIPTION
- Clear colourless or slightly yellowish liquid with a pungent odour. Various concentrations are supplied as products of commerce.
- FUNCTIONAL USES
- Acid
- METHOD OF ASSAY
- Tare accurately a 125-ml glass-stoppered conical flask containing 50 ml of 1N sodium hydroxide. Partially fill, without the use of vacuum, a 10-ml serological pipet from near the bottom of a representative sample, remove any acid adhering to the outside and discard the first ml flowing from the pipet. Hold the tip of the pipet just above the surface of the sodium hydroxide solution, and transfer between 2.5 and 3 ml of the sample into the flask, mix the contents, and weigh accurately to obtain the weight of the sample. Add methyl orange TS and titrate the excess of sodium hydroxide with 1N hydrochloric acid. Each ml of 1N sodium hydroxide is equivalent to 36.46 mg of HCl.
Identification
- Solubility (Vol. 4)
- Soluble in water and in ethanol
- Test for acid
- A 1 in 100 solution of the sample is acid to litmus paper
- Test for chloride (Vol. 4)
- Passes test
Purity criteria
- Non-volatile residue
- Not more than 0.5% Transfer 1 g into a tared glass dish, evaporate to dryness on a steam bath, dry at 110º for 1 h, cool in a desiccator and weigh. The weight of the residue does not exceed 5 mg.
- Reducing substances
- Not more than 70 mg/kg as sulfur dioxide ; Transfer 1 ml of reagent grade hydrochloric acid into a 30-ml test tube, dilute to 20 ml with freshly boiled and cooled water, and add 1 ml of potassium iodide TS, 1 ml of starch TS and 2 ml of 0.001N iodine. Stopper the test tube and mix thoroughly. The blue colour produced is not discharged by 1 ml of the sample.
- Oxidizing substances
- Not more than 30 mg/kg as chlorine Transfer 1 ml of the sample into a 30-ml test tube, dilute to 20 ml with freshly boiled and cooled water, and add 1 ml of potassium iodide TS and 1 ml of starch TS. Stopper the test tube and mix thoroughly. The intensity of any blue colour developed does not exceed that produced in a control prepared similarly but containing 1 ml of 0.001N iodine (instead of potassium iodide TS) and 1 ml of reagent grade concentrated hydrochloric acid (instead of sample).
- Sulfate
- Not more than 0.5% Dilute 1 g of the sample to 100 ml with water, transfer 5 ml of this dilution to a 50-ml tall-form Nessler tube and dilute to 20 ml with water. Add a drop of phenolphthalein TS, neutralize the solution with ammonia TS, and then add 1 ml of hydrochloric acid TS prepared from reagent grade hydrochloric acid. To the clear solution (filtered if necessary) add 3 ml of barium chloride TS, dilute to 50 ml with water and mix. Prepare a control consisting of 1 ml of reagent grade concentrated hydrochloric acid and 250 μg of sulfate (SO 4 ) and the same quantities of the reagents as used for the sample. Any turbidity shown in the sample does not exceed that in the control.
- Total organic compounds
- Total organic compounds (non-fluorine): Not more than 5 mg/kg Benzene: Not more than 0.05 mg/kg Fluorinated organic compounds (total): Not more than 25 mg/kg See description under TESTS
- Iron
- Not more than 5 mg/kg Dilute 5 g (4.3 ml) of the sample to 40 ml and add about 40 mg of ammonium persulfate and 10 ml of ammonium thiocyanate TS. Any red colour developed does not exceed that in a control prepared by mixing 2.5 ml of Iron standard solution in an equal volume of a solution containing the same quantities of reagent grade hydrochloric acid and the reagents as used in the test.
- Lead (Vol. 4)
- Not more than 1 mg/kg Determine using an atomic absorption technique appropriate to the specified level. The selection of sample size and method of sample preparation may be based on the principles of the method described in Volume 4, “Instrumental Methods.”
- Test: Organic compounds
- Carry out analyses by gas chromatography employing Vapour Partitioning or Solvent Extraction, depending upon the characteristics of the compound being determined. It is necessary, however, to use the Vapour Partitioning method for the determination of benzene. Vapour Partitioning Method This method is suitable for the determination of extractable organic compounds at 0.05 to 100 mg/kg but is most appropriate for organic compounds with a vapour pressure greater than 10 mm Hg at 25 o . Use a gas chromatograph equipped with a flame ionization detector and a 4-m x 2-mm (id) stainless-steel column packed with 15%, by weight, methyl trifluoropropyl silicone (DCFS 1265, or QF-1, or OV-210, or SP-2401) stationary phase on 80/100 mesh Gas Chrom R or the equivalent. A newly packed column should be conditioned at 120º and 30 ml/min helium flow for at least 2 h (preferably overnight) before it is attached to the detector. For analysis, the column is maintained isothermally at 105 o , the injection port and detector are maintained at 250 o , the carrier gas flow rate is set at 11 ml/min, fuel gas flows should be optimized for the gas chromatograph and detector in use. The experimental conditions may be changed as necessary for optimal resolution and sensitivity. The signal-to-noise ratio should be at least 10:1. Preparation of Standard Solutions Prepare a standard solution of the organic compounds to be quantitated in Hydrochloric Acid (known to be free of interfering impurities) at approximate concentrations of 5 mg/kg, or within ±50% of the concentrations in the samples to be analyzed. Place a stirring bar in a one-litre volumetric flask equipped with a ground-glass stopper, and tare the combination. Fill the flask with reagent-grade hydrochloric acid so that no air space is present when the flask is stoppered, and determine the weight of the Hydrochloric Acid. Calculate the volume (V) in 1l of each organic component to be added from the formula V = (C x W)/(D x 1000) where C is the desired concentration, in mg/kg; W is weight, in g, of the Hydrochloric Acid; D is the density, in mg/1l, of the organic compound; and 1000 is a conversion factor with the units g/kg. Add the calculated amount of each component to the Hydrochloric Acid with a syringe (ensure that the syringe tip is under the solution surface), stopper the flask, and stir the solution for at least 2 h using a magnetic stirrer. Calibration Treat the standard in the same way as described for the sample under Procedure (below). Determine a blank for each lot of reagent-grade Hydrochloric Acid, and calculate a response factor (R) by dividing the concentration (C) in mg/kg for each component by the peak area (A) for that component (subtract any area obtained from the blank sample): R - C/(A - area of blank) Gaseous compounds present special problems in the preparation of standards. Therefore, to determine response factors for gaseous compounds use the following method, which will be referred to as the Method of Multiple Extractions. Dilute a sample of Hydrochloric Acid known to contain the gaseous compound of interest with an equal volume of water. Draw 20 ml of this solution into a 50-ml glass syringe; then draw 20 ml of air into the syringe, cap with a rubber septum, and place the syringe on a shaker for 5 min. Withdraw 1 ml of the vapour through the septum, and inject it into the chromatograph. Expel the vapour phase from the 50-ml syringe, draw in another 20 ml of air, repeat the extraction, and inject another 1-ml vapour sample into the gas chromatograph. Repeat the extraction, and GC analysis on the same sample of acid a total of six times. For each impurity, plot the area (A N ) determined for extraction N against the difference between A N and the area determined for extraction (N + 1); that is, plot A N against [A N - A N+1 ]. The slope of this line is the extraction efficiency (E) for that impurity into the air. Inject into the chromatograph 1 ml of 0.1% (by volume) standard gas sample of each impurity in air and determine the absolute factor (F A ) in g, per peak area (A) by the following formula: F = (M x 4.0816 x 10 -8 )/A, A where M is the molecular weight of the compound. The concentration (C), in mg/kg, of the component in the original sample is calculated by the formula C = (A x F x 1.6949 x 10 6 )/E. A where A is the peak area corresponding to the compound (as above), F A is the absolute factor, and E is extraction efficiency. The response factor is then calculated as R = C/A Procedure Dilute a 10-ml sample of Hydrochloric Acid to be analyzed with an equal volume of water. Draw this solution into a 50-ml glass syringe. Then draw 20 ml of air into the syringe, cap with a rubber septum, and place the syringe on a shaker for 5 min. Draw 1 ml of the vapour through the septum, and inject it into the gas chromatograph. Approximate elution times in min for some specific organic compounds are as follows: Methane and acetylene: 1.70 Methyl chloride: 2.21 Vinyl chloride: 2.29 1,1,1-Trichlorofluoromethane: 2.62 Ethyl chloride: 2.90 Vinylidene chloride: 3.20 Methylene chloride: 3.64 Chloroform: 4.49 1,1-Dichloroethane: 4.53 Carbon tetrachloride: 4.86 1,1,1-Trichloroethane: 5.50 Benzene: 6.00 Trichloroethylene: 6.22 Ethylene dichloride: 6.61 Propylenedichloride: 8.41 Perchloroethylene: 9.73 Alternate columns may be required to resolve some combinations of components. Methyl chloride and vinyl chloride are resolved by a 3.7-m x 3-mm (id) squalene column at 45 o and a helium flow of 10 ml/min. Chloroform and 1,1-dichloroethane are resolved by a 4-m x 3-mm (id) DC 550R column at 110 o and a helium flow of 12 ml/min. Calculation Calculate the concentration (C) in mg/kg of each compound by multiplying its corresponding peak area (A) by the appropriate response factor (R) determined in the Calibration protocol: C = R x A Precision The relative standard deviation at 5 mg/kg should not exceed 15% for five analyses. Solvent Extraction Method The solvent extraction technique is suitable for the determination of extractable organic compounds at 0.3 to 100 mg/kg, but is most appropriate for organic compounds with vapour pressures less than 10 mm Hg at 25º. The conditions for the gas chromatograph are the same as for the Vapour Partitioning method, except that the column temperature is 120º, and the carrier-gas flow is 21 ml/min. Preparation of Standards Prepare the Standard Solution as described under Vapour Partitioning. Calibration Extract a sample of the Standard Solution as directed under Procedure (below) and inject it into the gas chromatograph. Determine a blank for each lot of reagent-grade Hydrochloric Acid and perchloroethylene by extracting the Hydrochloric Acid in the same way as the standard. Calculate a response factor (R) by dividing the concentration (C) in mg/kg for each component by the peak area (A) for that component (subtract any area obtained from the blank sample): R = C/(A - area of blank) Procedure Accurately transfer 90 ml of the Hydrochloric Acid sample and 10 ml of perchloroethylene (free of interfering impurities) into a narrow-mouth, 125-ml bottle. Place the bottle in a mechanical shaker for 30 min. Separate the two phases (perchloroethylene on the bottom) and inject 3 μl of the perchloroethylene extract into the gas chromatograph. Approximate elution times in min for some chlorinated organic compounds are as follows: Vinylidene chloride: 2.94 Methylene chloride: 3.27 Chloroform: 3.83 Carbon tetrachloride: 4.07 1,1,1-Trichloroethane: 4.50 Trichloroethylene: 4.97 Ethylene dichloride: 5.26 Propylene dichloride: 6.36 Perchloroethylene: 6.95 1,1,1,2-Tetrachloroethane: 10.12 1,1,2,2-Tetrachloroethane: 13.70 Pentachloroethane: 16.19 To determine perchloroethylene and higher-boiling impurities, substitute methylene chloride (free of interfering impurities) for perchloroethylene in the extraction step. For higher-boiling impurities such as monochlorobenzene and the three dichloro- benzenes, use a 2.74-m x 2.1-mm (id) stainless steel column packed with 10% Carbowax 20M/20% KOH on 80/100 mesh Chromasorb W (acid washed) at 150º and a nitrogen flow of 35 ml/min. Calculation Calculate the concentration (C), in mg/kg, of each compound by multiplying the corresponding peak area (A) (subtracted any area obtained from the blank sample) by the appropriate response factor (R) determined in the Calibration protocol: C = R x (A - area of blank) Precision The relative standard deviation at 5 mg/kg should not exceed 15% for five analyses.
Authorised in other additives, enzymes, flavourings and nutrients
These authorisations are not for use in food. They let this substance be used inside another additive, a food enzyme, a flavouring or a nutrient preparation — often as a carrier — and it reaches food only as part of that product. Annex III to Regulation (EC) No 1333/2008.
| Part | May be used in | Maximum level | Citation |
|---|---|---|---|
| Annex III, Part 2: Food additives other than carriers in food additives | All food additive preparationsAuthorised as a member of Table 1 of Part 6, listed as "Table 1" Note (1): Except enzymes authorised as food additives. | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 2, via Table 1 of Part 6 |
| Annex III, Part 3: Food additives including carriers in food enzymes | Food enzymesCan be used as a carrier: Yes Note (1): Including enzymes authorised as food additives. | In enzyme preparation: quantum satis In final food except beverages: quantum satis In beverages: quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 3 |
| Annex III, Part 4: Food additives including carriers in food flavourings | All flavouringsAuthorised as a member of Table 1 of Part 6, listed as "Table 1" | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 4, via Table 1 of Part 6 |
| Annex III, Part 5, Section A: Food additives added in nutrients except in nutrients intended to be used in foodstuffs listed in Part E, point 01.10, of Annex II and foodstuffs for infants and young children listed in Part E, point 13.1, of Annex II | All nutrientsCan be used as a carrier: Yes | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 5, Section A |
Every name it appears under
88 recorded names. A label may use any of them.
E number
- E507
INS number
- 507
CAS registry number
- 7647-01-0
As it appears in regulation
- Hydrochloric acid
Other names
- 4-D Bowl Sanitizer
- Acid, Hydrochloric
- Acid, Muriatic
- Acide chlorhydrique
- Acido clorhidrico
- Acido cloridrico
- Acidum hydrochloricum
- Acidum Muriaticum
- Anhydrous hydrochloric acid
- Anhydrous hydrogen chloride
- Aqueous hydrogen chloride
- Baume hcl
- Bowl Cleaner
- Caswell No. 486
- Chloorwaterstof
- chlorane
- chlorhydric acid
- Chloride, Hydrogen
- Chlorohydric acid
- Chlorowodor
- chlorure d'hydrogene
- Chlorure d'hydrogene anhydre
- Chloruro de hidrogeno
- Chlorwasserstoff
- cloruro de hidrogeno
- Cloruro de hidrogeno anhidro
- Deuterium-chloride
- E 507
- Emulsion Bowl Cleaner
- Enplate po 236
- EPA Pesticide Chemical Code 045901
- Funoran
- HCl
- HEMMORHOIDS
- HSDB 545
- Hydrochloric acid
- Hydrochloric acid gas
- Hydrochloric acid, ACS reagent, 37%
- Hydrochloric acid, anhydrous
- hydrochloricacid
- Hydrogen chloride
- Hydrogen chloride (acid)
- Hydrogen chloride (gas only)
- Hydrogen chloride (HCl)
- Hydrogen Chloride - Methanol Reagent
- Hydrogenchlorid
- Hygeia Creme Magic Bowl Cleaner
- Icon etch
- INS NO.507
- INS-507
- Marine acid
- mono hydrochloride
- monohydrochloride
- Muriatic acid
- Muriaticum acidum
- Percleen Bowl and Urinal Cleaner
- UN 1050 (anhydrous)
- UN 2186 (refrigerated liquefied gas)
- White Emulsion Bowl Cleaner
Systematic names
- hydrogen chloride
Hazard reference values
| Type | Value | Population | Assessed by | Opinion |
|---|---|---|---|---|
| ADI | not limited | — | JECFA | 1965 |
Evidence and how bodies read it
What assessing bodies concluded
Each conclusion is paraphrased in the body's own framing, from the published opinion linked beneath it. Where bodies differ, both stand; this site does not adjudicate between them or add a view of its own.
EFSA 2019
The FAF Panel found no concern for genotoxicity or carcinogenicity for hydrochloric acid and its potassium, calcium and magnesium salts (E 507–E 509, E 511), and used a human reference value of 40 mg chloride/kg bw/day. Although high-percentile exposure in toddlers, children and adolescents was slightly above that value, it concluded that exposure to chloride from these additives does not raise a safety concern at reported uses.
Common questions
Assembled from what is above, in the words the questions are usually asked in. Each answer is the same statement the relevant section makes, with the same citations behind it.
- What is E 507?
- E 507 is Hydrochloric acid. Hydrochloric acid is used as a processing aid and acidity regulator, chiefly to hydrolyse proteins and starches and to adjust pH during manufacture. It is generally neutralised before the food is finished.
- What is Hydrochloric acid used for in food?
- It is listed as an acidity regulator — the role Canada, Codex and the US assign it. This page shows every function each regulator records, with the citation for each.
- Where is Hydrochloric acid permitted?
- Of the seven regulators this site reads, Australia and New Zealand, Canada, the EU, Great Britain, Japan, South Korea, the US and the Codex standard permit it. Each permission is for named foods at named levels, not a blanket one; the table on this page gives them with citations.
- Is Hydrochloric acid vegan?
- Yes. Hydrochloric acid is not derived from animals, and is suitable for vegetarians. This page says what it is made from and how.
Sources for this page
- anz retrieved 2026-10-17
- ca retrieved 2026-10-17
- eu retrieved 2026-10-18
- gb retrieved 2026-10-18
- jp retrieved 2026-10-18
- kr retrieved 2026-10-18
- ecfr retrieved 2026-10-17
- gsfa retrieved 2026-09-07
- euspecs retrieved 2026-10-18
- jecfaspecs retrieved 2026-09-23
Full licence terms and publisher details on Sources. How this page is built and updated: Method.
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