Benzoic Acid

HCID 243CAS 65-85-0

Basic information

Standard SMILES
O=C(O)c1ccccc1
InChIKey
WPYMKLBDIGXBTP-UHFFFAOYSA-N
Molecular formula
C7H6O2
Average molar mass
122.12 g/mol
Monoisotopic mass
122.03677943

Names & identifiers

Preferred name
Benzoic Acid
IUPAC
benzoic acid
English name
Benzoic acid
Molecular formula
C7H6O2
Molecular weight
122.12

Names & synonyms

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

Database identifiers

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

Properties

Computed structural properties

XLogP
1.9
Topological polar surface area
37.3 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
2
Rotatable bonds
1
Heavy atoms
9

Experimental & physicochemical properties

pH · 2 items

About 4 (solution in water)

pH = 2.8 (Saturated soln at 25 °C)

LogP · 4 items

1.87

log Kow = 1.87

1.87

1.87

LogS-1.55
Odor · 2 items

Odorless or with a slight benzaldehyde odor

FAINT, PLEASANT ODOR

Taste · 3 items

ALMOST TASTELESS /BENZOIC ACID USP/

BITTER TASTE

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

Density · 6 items

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

Physicochemical properties

Melting point
121 · 121-125 °C(lit.)
Boiling point
249 °C · 249 °C(lit.)
Density
1.08 · 1.08
bulk density
500 kg/m3 · 500kg/m3
vapor density
4.21 · 4.21 (vs air)
vapor pressure
10 mm · 10 mm Hg ( 132 °C)

Safety & regulation

GHS classification

GHS Classification · 6 items

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.

Hazard information

Regulatory Information · 6 items

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 items

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 items

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 item

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.

Safety & protection

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

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 item

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 item

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.

Toxicology

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 items

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 item

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 items

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 items

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 item

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).

Regulatory information

Regulatory Information · 6 items

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 items

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 items

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 item

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 item

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 item

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.

Safety data

F
21
PPE
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
wgk
1
tsca
TSCA listed
rtecs
DG0875000
ridadr
UN 3077 9/PG 3

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 6 items

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 items

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 items

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 items

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

Uses & manufacturing

Uses · 6 items

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 items

(1972) 2.9X10+8 G

(1975) 8.67X10+8 G

U.S. Imports · 3 items

(1972) NEGLIGIBLE

(1975) 6.04X10+7 G

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

U.S. Production · 6 items

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 items

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
Applications · 7 items

Uses1. Used as a chemical reagent and preservative. 2. Benzoic acid is important type food preservative. Under acidic conditions, It has inhibitory effects to mold, yeast and bacteria , but the effect is weak acid producing bacteria. The most appropriate antimicrobial pH values is ranging from 2.5 to 4, generally lower, the pH value is appropriate from 4.5 to 5. In the food industry with plastic barrels concentrated fruit and vegetable juice, the maximum use amount shall not be over 2.0g/kg; in jam (excluding canned), (taste) juice drink, soy sauce, vinegar in the maximum dose of 1.0g/kg; in soft candy, wine, wine in the maximum dose of 0.8 g/kg separately; in the low salt pickled vegetables, the sauce, candied fruit, maximum dose is 0.5 g/kg; in carbonated drinks in the largest amount of use is 0.2g/kg. due to benzoic acid, slightly soluble in water, its use can be a small amount of ethanol enable dissolved. 3.Preservative; anti microbial agents. Due to the low solubility of benzoic acid and use shall be stirring, or dissolved in a small amount of hot water or ethanol. When used in the soft drink with fruit juice concentrate, for benzoic acid easy volatile with the water vapor, so often used in the sodium salt, besides the above sodium equivalent to benzoic acid 0.847g. 4.Often used as a fixative agent or preservative. Also used as a fruit juice aroma conservation agents. As a perfume with perfume fragrance. Can also be used for chocolate, lemon, orange, berries, nuts, candied fruit type edible essence. Tobacco flavor is also commonly used. 5.Benzoic acid and its sodium salt are food preservatives. Under acidic conditions, it has inhibition of yeasts and molds. When pH 3, antibacterial strength and when pH 6, many fungi effect is very poor, so the antibacterial optimum pH is 2.5-4.0. Benzoic acid is mainly used for the production of sodium benzoate preservatives, dyes intermediates, pesticides, plasticizers, mordant, medicine, spice and also can be used as alkyd resin and polyamide resin modifier for the production of polyester, terephthalic acid and used equipment, iron and steel anti rust agent. 6.Mainly used for antifungal and antiseptic. 7.Used in medicine, dye carriers, plasticizer, spices and food preservatives such as production, and can also be used to paint of alkyd resin performance improvement; used as pharmaceutical and dye intermediates, used for the preparation of plasticizer and spices etc., as well as equipment, iron and steel anti rust agent.

DescriptionBenzoic acid is a colorless, crystalline solid also known as benzenecarboxylic acid. It is the simplest aromatic carboxylic acid, with a carboxyl group (-COOH) bonded directly to the benzene ring. It is found naturally in the benzoin resin of a number of plants.

OccurrenceReported found in fresh apple, apricot (Prunus armeniaca L.), strawberry fruit, cherry (Prunus cerasus L.), butter, boiled and cooked beef, pork fat, white wine, black tea, green tea, fresh plum, mushroom, Bourbon vanilla (Vanilla planifolia Andrews), and other natural sources. Reported as being a constituent of various oils, resins and flower absolutes; hyacinth, tuberose, neroli bigarade, Chinese cinnamon, cinnamon leaves, anise, vertiver, ylang-ylang, Tolu balsam and clove; it is contained in fairly sizable amounts in gum benzoin, from which benzoic acid is extracted by sublimation.

HistoryBenzoic acid was first isolated from the dry distillation of benzoin by Blaise de Vigenère (1523–1596) in the 16th century. Friedrich Whler (1800–1882) and Justus von Liebig (1803–1873) prepared benzoic acid from oxidizing bitter almond oil (benzaldehyde) in 1832 and determined the formula for each of these compounds. They proposed that bitter almond oil, C7H6O, and benzoic acid were derivatives from the benzoyl radical, C7H5O; the radical theory was a major early theory in the development of organic chemistry.

UsesCalorimetry Benzoic acid is the most commonly used chemical standard to determine the heat of capacity of a bomb calorimeter. Feed stock Benzoic acid is used to make a large number of chemicals, important examples of which are : Benzoyl chloride, C6H5C(O)Cl, is obtained by treatment of benzoic with thionyl chloride, phosgene or one of the chlorides of phosphorus. C6H5C(O) Cl is an important starting material for several benzoic acid derivates like benzyl benzoate, which is used in artificial flavours and insect repellents. Food preservative Benzoic acid and its salts are used as a food preservatives, represented by the E-numbers E210 , E211 , E212 , and E213 . Benzoic acid inhibits the growth of mold, yeast and some bacteria. It is either added directly or created from reactions with its sodium, potassium, or calcium salt. The mechanism starts with the absorption of benzoic acid in to the cell. Medicinal Benzoic acid is a constituent of Whitfiel's ointment which is used for the treatment of fungal skin diseases such as tinea, ringworm, and athlete's foot. As the principal component of benzoin resin, benzoic acid is also a major ingredient in both tincture of benzoin and Fria's balsam. Such products have a long history of use as topical antiseptics and inhalant decongestants. Benzoic acid was used as an expectorant, analgesic, and antiseptic in the early 20th century.

UsesSodium 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.

General DescriptionBoric acid,H3B03, also known as boracic acid, orthoboric acid, and sassolite, is a white solid composed of triclinic crystals.It is a derivative of barium oxide and is soluble in water. A white crystalline solid. Slightly soluble in water. The primary hazard is the potential for environmental damage if released. Immediate steps should be taken to limit spread to the environment. Used to make other chemicals, as a food preservative, and for other uses.

Preparation methods · 2 items

PreparationIndustrial preparation method The industrial benzoic acid is mainly by toluene liquid phase air oxidation preparation. The process was with cobalt naphthenate as catalyst, in response to temperature is 140-160 ℃ and operating pressure is 0.2-0.3MPa and response generation benzoic acid. Reaction after steaming to toluene, and vacuum distillation and recrystallization to obtain the product. The process uses cheap raw materials, high yield. Therefore, it is industrial uses mainly the method. Laboratory preparation method of the main reaction: 1.C6H5CH3+ KMnO4+H2O-C6H5 COOK+KOH+MnO2+H2O(water in fron of the manganese dioxide is supplied with water reaction environment) 2.C6H5 COOK+HCl--C6H5 COOH Drug and dosage: Toluene 1.5g (1.7ml, 0.016mol), potassium permanganate 5g (0.032mol), CTAB(cetyl trimethyl ammonium bromide) 0.1g. Experimental operation: With 100 ml round bottom flask. Install a refluxing device. add 5g potassium permanganate, 0.1g of hexadecyl trimethyl ammonium bromide, 1.7 ml of toluene and 50 ml of water to the reaction flask, stir heated boiling (vigorous stirring, violent boiling), keep the reactant solution stable boiling. When large amounts of brown precipitate, potassium permanganate purple shallow or disappeared, the toluene layer disappeared, reaction has basically ended. Filter out of manganese dioxide precipitation, landfill leachate by concentrated hydrochloric acid, precipitation of benzoic acid precipitation, filtering to the crude product. The crude product water recrystallization. In a boiling water bath for drying, weighing, measuring the melting point.

PreparationBy oxidation of toluene with nitric acid or sodium bichromate or from benzonitrile.

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国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
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衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Benzoic acid is a compound comprising a benzene ring core carrying a carboxylic acid substituent. It has a role as an antimicrobial food preservative, an EC 3.1.1.3 (triacylglycerol lipase) inhibitor, an EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor, a plant metabolite, a human xenobiotic metabolite, an algal metabolite and a drug allergen. It is a conjugate acid of a benzoate.

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