Benzoesure

Benzoic Acid

HCID 243CAS 65-85-0

Grundinformationen

Standard-SMILES
O=C(O)c1ccccc1
InChIKey
WPYMKLBDIGXBTP-UHFFFAOYSA-N
Summenformel
C7H6O2
Durchschnittliche Molmasse
122,12 g/mol
Monoisotopische Masse
122,03677943

Namen und Bezeichner

Bevorzugter Name
Benzoic Acid
IUPAC
benzoic acid
Lokaler Name
Benzoesure
Englischer Name
Benzoic acid
Summenformel
C7H6O2
Molmasse
122.12

Namen und Synonyme

benzoic acid65-85-0Dracylic acidbenzenecarboxylic acidBenzeneformic acidCarboxybenzenephenylformic acidBenzenemethanoic acidPhenylcarboxylic acidRetardexRetarder BATenn-Plas
Weitere Namen anzeigen
Benzyl acidBenzoic acid, for analysis ACSNipacideBenzoic aBenzoic acidcidFEMA 2131a 1 (acid)Benzoic acid naturalBenzoesure
Salvo liquidBenzoesaeure GKBenzoesaeure GVAcide benzoiqueSolvo powderBenzoic acid, tech.Unisept BZABenzoesaeure

Datenbank-Bezeichner

CAS
65-85-0
PubChem CID
243
DTXSID
DTXSID6020143
ChEMBL
CHEMBL541
ChEBI
CHEBI:30746
UNII
8SKN0B0MIM
EC Number
200-618-2
Nikkaji
J2.358B

Eigenschaften

Berechnete Struktureigenschaften

XLogP
1,9
Polarare Oberfläche (TPSA)
37,3 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
1
Schwere Atome
9

Experimentelle und physikochemische Eigenschaften

pH · 2 Einträge

About 4 (solution in water)

pH = 2.8 (Saturated soln at 25 °C)

LogP · 4 Einträge

1.87

log Kow = 1.87

1.87

1.87

LogS-1.55
Odor · 2 Einträge

Odorless or with a slight benzaldehyde odor

FAINT, PLEASANT ODOR

Taste · 3 Einträge

ALMOST TASTELESS /BENZOIC ACID USP/

BITTER TASTE

Taste detection 8.5X10+1 ppm /Media and purity not specified/

Density · 6 Einträge

1.316 at 82.4 °F (USCG, 1999) - Denser than water; will sink

1.2659 g/cu cm at 15 °C

Sp gr: 1.316 at 24 °C/4 °C (solid); 1.029 at 180 °C/4 °C (liquid)

1.3 g/cm³

Relative density of the vapour/air-mixture at 20 °C (air = 1): 1

1.316 @ 15°C

Physikochemische Eigenschaften

Schmelzpunkt
121 · 121-125 °C(lit.)
Siedepunkt
249 °C · 249 °C(lit.)
Dichte
1.08 · 1.08
Dampfdichte
4.21 · 4.21 (vs air)
Dampfdruck
10 mm · 10 mm Hg ( 132 °C)
Brechungsindex
1.504 · 1.504

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H315: Causes skin irritation [Warning Skin corrosion/irritation];H318: Causes serious eye damage [Danger Serious eye damage/eye irritation];H372: Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure]

P260, P264, P264+P265, P270, P280, P302+P352, P305+P354+P338, P317, P319, P321, P332+P317, P362+P364, and P501 (click each P-code to see the statement)

This chemical does not meet GHS hazard criteria for 0.9% (28 of 3274) of reports.

Gefahrenhinweise

Regulatory Information · 6 Einträge

Chemical: Benzoic acid

Regulation (EC) No 1831/2003 (amended)

Benzoic acid is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzoic acid are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

04/30/EC, Reg. (EU) 2016/2016, Reg. (EU) 2017/1113, Reg. (EU) No 540/2011, Reg. (EU) No 823/2012

Status: Active Update: 30-10-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/13124

Benzoic acid: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Benzoic acid: Environment tier I assessment;IMAP assessments - Benzoic acid: Human health tier II assessment
Fire Hazards · 2 Einträge

Behavior in Fire: Vapor from molten benzoic acid may form explosive mixture with air. Concentrated dust may form explosive mixture. (USCG, 1999)

Combustible. Finely dispersed particles form explosive mixtures in air. Risk of fire and explosion on contact with incompatible substances. See Chemical Dangers.

Fire Potential · 2 Einträge

Slight, when exposed to heat or flame...

Benzoic acid is burned in oxygen as primary thermochemical standard to calibrate oxygen bomb calorimeters used in... determination of calorific value of liquid hydrocarbon fuels. If the benzoic acid is powdered (rather than pelleted...), very rapid combustion occurs and flame front may burn through the non-metallic... seals on valve seats and the bomb may be destroyed.

Health HazardsDust may be irritating to nose and eyes. At elevated temperatures, fumes may cause irritation of eyes, respiratory system, and skin. (USCG, 1999)
Hazards Summary · 1 Eintrag

A skin and eye irritant; [ICSC] Causes non-immunological contact urticaria; [Kanerva, p. 218] Benzoic acid alkali salts cause pseudoallergic reactions; [MAK] TLV Basis: Irritation of eye and respiratory tract, and lung damage; Low level oral exposures are considered safe . . . [ACGIH] See Sodium benzoate and Potassium benzoate.

Sicherheit und Schutzausrüstung

Fire FightingUse water spray, powder, foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
First Aid Measures · 4 Einträge

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Refer for medical attention .

First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.;SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment.;INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing.;INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

Safe StorageStore only in original container. Separated from incompatible materials. See Chemical Dangers. Fireproof. Store in an area without drain or sewer access.
Exposure Control and Personal Protection0.5 [mg/m3], respirable fraction (2 mg/m3, inhalable fraction)[German Research Foundation (DFG)]
Fire Fighting Procedures · 1 Eintrag

If material on fire or involved in fire: Use water in flooding quantities as fog. Solid streams of water may spread fire. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use foam, dry chemical, or carbon dioxide.

Toxikologische Informationen

Body BurdenBenzoic acid was found in one of twelve breath samples taken from people in New Jersey. Benzoic acid was not found in the drinking water or air samples from this study(1).
Interactions · 4 Einträge

The metabolism of the benzoates depletes glycine concentrations and can therefore alter the glycine-dependent metabolism of other compounds. /Investigators/ demonstrated that benzoic acid or sodium benzoate successfully competed with aspirin for glycine, resulting in increased concentration and persistence of salicylic acid in the body. Almost total inhibition of salicyluric acid formation in humans was achieved using either 2.7 g benzoic acid or 3.2 g sodium benzoate.

In rat liver microsomes deferoxamine was a potent inhibitor of the oxidation of the scavenging agent, benzoate. Nearly complete inhibition was observed at 33-100 uM.

Groups of 25 male and 25 female mice were given benzoic acid at a dose of 40 mg/kg bw/day, sodium bisulfite at 80 mg/kg bw/day, or a mixture of the two for 17 months. Mortality was greater in the groups receiving the mixture (62%) than in those receiving the individual substances (32%) at eight months.

Wistar rats /were administered/ 40 mg benzoic acid/kg/day and 80 mg sodium bisulphite/kg/day once daily /for/ 72 weeks. 50 rats /with/ initial body weight /of/ 100-120g /experienced/ reduced weight gain, kidney function and reaction on stress factors were altered (no further information), /and/ the erythrocyte sedimentation rate was increased.

Health Effects · 1 Eintrag

People must absorb small amounts of copper every day because copper is essential for good health, however, high levels of copper can be harmful. Very-high doses of copper can cause damage to your liver and kidneys, and can even cause death. Copper may induce allergic responses in sensitive individuals. (L278, L279)

Ecotoxicity Values · 5 Einträge

LC50; Species: Colinus virginianus (Northern bobwhite quail) diet >5620 ppm for 8 days

LC50; Species: Anas platyrhynchos (Mallard duck) diet >5620 ppm for 8 days

LD50; Species: Anas platyrhynchos (Mallard duck) oral via capsule >2510 mg/kg

EC50; Species: Anabaena inaequalis (Cyanobacteria); Conditions: static; Concentration: 9 mg/L for 14 days; Effect: cell multiplication inhibition

For more Ecotoxicity Values (Complete) data for BENZOIC ACID (16 total), please visit the HSDB record page.

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 15(SRC), determined from a structure estimation method(2), indicates that benzoic acid is expected to have very high mobility in soil(SRC). The pKa of benzoic acid is 4.20(3), indicating that this compound will exist almost entirely in the anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4). Volatilization from moist soil is not expected because the compound exists as an anion and anions do not volatilize. Benzoic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 7.0X10-4 mm Hg at 25 °C(5). Mineralization half-life in Captina silt loam for benzoic acid in solution was 4.5 hr after a 30 minute lag(6) and complete degradation occurred in 1 day using a Niagra silt loam inoculum(7), suggesting that biodegradation may be an important fate process in soil(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 15(SRC), determined from a structure estimation method(2), indicates that benzoic acid is not expected to adsorb to suspended solids and sediment(SRC). A pKa of 4.20(3) indicates benzoic acid will exist almost entirely in the anion form at pH values of 5 to 9 and, therefore, volatilization from water or moist soil surfaces is not expected to be an important fate process(SRC). According to a classification scheme(4), a BCF range of <10 to 21(5) suggests the potential for bioconcentration in aquatic organisms is low(SRC). Biodegradation half-lives of 0.85 and 3.6 days using inoculum from a polluted river and a reservoir, respectively(6), suggest that biodegradation may be an important fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), benzoic acid, which has a vapor pressure of 7X10-4 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase benzoic acid is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 9 days(SRC), calculated from its rate constant of 1.2X10-12 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Benzoic acid absorbs light at wavelengths >290 nm(4) and, therefore, may be expected to be susceptible to direct photolysis by sunlight(SRC).

Food Survey Values · 1 Eintrag

Apple wine and apple essence contain 0.329 and 40 ppm of benzoic acid, respectively(1). Benzoic acid and sodium benzoate are common food additives, being used as food preservatives at a concentration of 0.1% and as antimicrobial agents in food at concentration levels of 0.29-0.00001%(1). Most berries contain about 0.05% of benzoic acid(2). Benzoic acid has been detected but not quantified in pine sprout tea(3). Benzoic acid has been detected in concentrations of 10, 50, 10, and <5 ppb in canned creamed, canned kernel, frozen kernel, and fresh kernel sweet corn, respectively(4). Benzoic acid was detected in fine particle organic matter emitted from Chinese cooking. Four representative restaurants in Guangzhou city, China: Cantonese style (fresh local ingredients, lightly seasoned, stir fry, peanut and blended oil); Hunan style (spicy and sour dishes, steamed, peanut oil); Sichuan style (sharp and spicy, sauteing, blended oil), and Dongbei style (home-cooking, pot roast, simmering, marinating, canola and peanut oil) Average benzoic acid concentrations in fine particulates were 39, 17, 30, and 20 ng/mg of POM (particulate organic matter), respectively(5).

Regulatorische Informationen

Regulatory Information · 6 Einträge

Chemical: Benzoic acid

Regulation (EC) No 1831/2003 (amended)

Benzoic acid is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzoic acid are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

04/30/EC, Reg. (EU) 2016/2016, Reg. (EU) 2017/1113, Reg. (EU) No 540/2011, Reg. (EU) No 823/2012

Status: Active Update: 30-10-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/13124

Benzoic acid: Does not have an individual approval but may be used under an appropriate group standard

FDA Requirements · 5 Einträge

Substance added directly to human food affirmed as generally recognized as safe (GRAS). Current usage results in a max level of 0.1% in food.

This substance is generally recognized as safe for use at a level not exceeding 0.1 percent in accordance with good manufacturing or feeding practice.

Drug products containing certain active ingredients offered over-the-counter (OTC) for certain uses. A number of active ingredients have been present in OTC drug products for various uses, as described below. However, based on evidence currently available, there are inadequate data to establish general recognition of the safety and effectiveness of these ingredients for the specified uses: Benzoic acid is included in topical acne drug products.

Drug products containing certain active ingredients offered over-the-counter (OTC) for certain uses. A number of active ingredients have been present in OTC drug products for various uses, as described below. However, based on evidence currently available, there are inadequate data to establish general recognition of the safety and effectiveness of these ingredients for the specified uses: Benzoic acid is included in skin protectant drug products.

Drug products containing certain active ingredients offered over-the-counter (OTC) for certain uses. A number of active ingredients have been present in OTC drug products for various uses, as described below. However, based on evidence currently available, there are inadequate data to establish general recognition of the safety and effectiveness of these ingredients for the specified uses: Benzoic acid is included in topical antifungal drug products.

FIFRA Requirements · 3 Einträge

Residues of benzoic acid are exempted from the requirement of a tolerance when used in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops or to raw agricultural commodities after harvest. Use: preservative for formulations.

Residues of benzoic acid are exempted from the requirement of a tolerance when used in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to animals. Use: preservative for formulations.

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer saftey standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Benzoic acid is found on List D. Case No: 4013; Pesticide type: Insecticide, fungicide; Case Status: OPP is reviewing data from the pesticide's producers regarding its human health and/or environmental effects, or OPP is determining the pesticide's eligibility for reregistration and developing the Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): Benzoic acid; AI Status: The active ingredient is no longer contained in any registered pesticide products ... "cancelled."

Atmospheric Standards · 1 Eintrag

This action promulgates standards of performance for equipment leaks of Volatile Organic Compounds (VOC) in the Synthetic Organic Chemical Manufacturing Industry (SOCMI). The intended effect of these standards is to require all newly constructed, modified, and reconstructed SOCMI process units to use the best demonstrated system of continuous emission reduction for equipment leaks of VOC, considering costs, non air quality health and environmental impact and energy requirements. Benzoic acid is produced, as an intermediate or a final product, by process units covered under this subpart.

CERCLA Reportable Quantities · 1 Eintrag

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 5000 lb or 2270 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

Clean Water Act Requirements · 1 Eintrag

Benzoic acid is designated as a hazardous substance under section 311(b)(2)(A) of the Federal Water Pollution Control Act and further regulated by the Clean Water Act Amendments of 1977 and 1978. These regulations apply to discharges of this substance. This designation includes any isomers and hydrates, as well as any solutions and mixtures containing this substance.

Sicherheitsdaten

F
21
wgk
1
tsca
TSCA listed
ridadr
UN 3077 9/PG 3
hs_code
2916 31 00
RTECS-Nr.
DG0875000

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 6 Einträge

Benzoic acid ... conjugated with glycine to give hippuric acid in ... many mammals (man, monkeys, pig, rabbit, rodents, cat, dog, ferret & hedgehog). Dog, ferret, & hedgehog also excreted ... benzoyl glucuronide ... but indian fruit bat excreted almost all dose as benzoyl glucuronide.

/Investigators/ demonstrated that biotransformation of benzoic acid to hippuric acid follows saturable or Michaelis-Menten kinetics in humans following ingestion of sodium benzoate. /Sodium Benzoate/

The availability of glycine was the rate-limiting factor in the formation of hippuric acid. When insufficient glycine was available benzoyl glucuronide was formed.

/Investigators/ reported that both lipoic acid and valproic acid reduced the clearance of benzoic acid in rats that had been "loaded" with glycine. Both acids reduced the availability of hepatic coenzyme A that is needed for the adenosine triphosphate (ATP)-dependent conjugation with glycine.

For more Metabolism/Metabolites (Complete) data for BENZOIC ACID (11 total), please visit the HSDB record page.

Benzoic acid has known human metabolites that include Benzoyl glucuronide.

FDA Pharmacological Classification · 6 Einträge

8SKN0B0MIM

BENZOIC ACID

Mechanisms of Action [MoA] - Ammonium Ion Binding Activity

Established Pharmacologic Class [EPC] - Nitrogen Binding Agent

Benzoic acid is a Nitrogen Binding Agent. The mechanism of action of benzoic acid is as an Ammonium Ion Binding Activity.

ACIDUM BENZOICUM

MeSH Pharmacological Classification · 2 Einträge

Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues.

Substances capable of inhibiting, retarding or arresting the process of fermentation, acidification or other deterioration of foods.

Absorption, Distribution and Excretion · 5 Einträge

After oral ingestion of benzoic acid and sodium benzoate, there is a rapid absorption (of undissociated benzoic acid) from the gastrointestinal tract in experimental animals or humans. ... 100% absorption can be assumed. In humans, the peak plasma concentration is reached within 1-2 hr.

Experiments on the distribution and elimination of (14)C-benzoate in the rat have shown no accumulation of sodium benzoate or benzoic acid in the body.

Benzoic acid and sodium benzoate are rapidly absorbed from the gastrointestinal tract of mammals and conjugated with glycine in the liver. The resulting hippuric acid is excreted in the urine rapidly (75% to 100% of the dose is excreted within 6 hours; the remaining dose is excreted within 2 to 3 days).

/Investigators/ reported that 42.6% +/-16.5% of a dermally applied (14)C-Benzoic acid dose (4 ug/sq cm; in acetone) was excreted in the urine within 24 hours. When applied in petrolatum, 60.5% of the dose was absorbed.

For more Absorption, Distribution and Excretion (Complete) data for BENZOIC ACID (17 total), please visit the HSDB record page.

Tissue LocationsBladder;Epidermis;Fibroblasts;Kidney;Liver;Placenta;Testis
Cellular LocationsCytoplasm;Endoplasmic reticulum;Extracellular

Verwendung und Herstellung

Uses · 6 Einträge

CIR ingredient: Benzoic Acid

Used as a food and drug preservative; Used as a chemical standard and intermediate; [HSDB]

No longer contained in any registered pesticide products; Cancelled by EPA; [HSDB]

For Benzoic acid (USEPA/OPP Pesticide Code: 009101) there are 0 labels match. /SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

The active ingredient is no longer contained in any registered pesticide products ... "cancelled."

The largest use of benzoic acid is as a chemical raw material in the production of phenol, caprolactam, glycol dibenzoates esters, and sodium and/or potassium benzoate.

U.S. Exports · 2 Einträge

(1972) 2.9X10+8 G

(1975) 8.67X10+8 G

U.S. Imports · 3 Einträge

(1972) NEGLIGIBLE

(1975) 6.04X10+7 G

(1984) 3.87X10+8 g /Summation of two report items for Benzoic Acid/

U.S. Production · 6 Einträge

2023: 100,000,000 - <250,000,000 lb;2022: 100,000,000 - <250,000,000 lb;2021: 100,000,000 - <250,000,000 lb;2020: 100,000,000 - <250,000,000 lb

(1972) 7.06X10+10 G

(1975) 2.87X10+10 G

(1991) 2.68x10+8 lb

Benzoic acid is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).

For more U.S. Production (Complete) data for BENZOIC ACID (8 total), please visit the HSDB record page.

Consumption Patterns · 3 Einträge

CHEMICAL PROFILE: Benzoic Acid. Phenol, 55%; benzoate plasticizers, 22%; sodium and potassium benzoate, 8%; benzoylchloride, 7%; alkylated resins, 3%; others, including butyl benzoate, sucrose benzoate, USP applications and exports, 5%.

CHEMICAL PROFILE: Benzoic acid. Demand: 1986: 160 million lb; 1987: 163 million lb; 1991 /projected/: 175 million lb.

The majority of the benzoic acid is utilized captively to produce phenol. The rest comes onto the market. Beverages and food applications accounted for 41% of world consumption of benzoic acid as sodium and potassium benzoate in 2006.

Consumer UsesOther;pH regulating agent;Stabilizing agent;Preservative;Not Known or Reasonably Ascertainable;Plasticizer;Etching agent;Intermediate
Anwendungen · 1 Eintrag

VerwendenSodium benzoate is an important benzoic acid derivative produced industrially by neutralization of benzoic acid using sodium hydroxide or sodium bicarbonate solution. Calcium benzoate, potassium benzoate, and other benzoate salts are also produced. Benzoic acid and sodium benzoate (C6H5COONa) are used as food preservatives and added to foods, juices, and beverages that are acidic.

Anbieter50 Anbieter

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