Benzyl benzoate CAS 120-51-4
Introduction：Basic information about Benzyl benzoate CAS 120-51-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Benzyl benzoate Basic informationDescription Chemical Properties Uses Preparation toxicity References
| Product Name: | Benzyl benzoate |
| Synonyms: | Benzyl benzoate ReagentPlus(R), >=99.0%;Benzyl benzoate Vetec(TM) reagent grade, 98%;Benzoic acid benzyl ester≥ 99% (GC);VANZOATE(R);VENZONATE(R);Benylate;Benzyl alcohol benzoic ester;Benzyl ester |
| CAS: | 120-51-4 |
| MF: | C14H12O2 |
| MW: | 212.24 |
| EINECS: | 204-402-9 |
| Product Categories: | CYSTADANE;Building Blocks;C12 to C63;Carbonyl Compounds;Chemical Synthesis;Esters;Aromatic Esters;Piperazine derivates;organic chemical;Nutrition Research;Organic Building Blocks;Phytochemicals by Plant (Food/Spice/Herb);Vaccinium macrocarpon (Cranberry);Chemical;INORGANIC & ORGANIC CHEMICALS;Solvent;120-51-4;11 |
| Mol File: | 120-51-4.mol |
Benzyl benzoate Chemical Properties
| Melting point | 17-20 °C (lit.) |
| Boiling point | 323-324 °C (lit.) |
| density | 1.118 g/mL at 20 °C (lit.) |
| vapor pressure | 1 mm Hg ( 125 °C) |
| refractive index | n |
| FEMA | 2138 | BENZYL BENZOATE |
| Fp | 298 °F |
| storage temp. | 2-8°C |
| solubility | Miscible with ethanol, alcohol, chloroform, ether, oils. |
| form | Liquid |
| color | Clear colorless |
| Odor | at 100.00 %. faint sweet balsam oily herbal |
| Odor Type | balsamic |
| biological source | synthetic |
| Water Solubility | practically insoluble |
| Merck | 14,1127 |
| JECFA Number | 24 |
| BRN | 2049280 |
| Dielectric constant | 4.8（20℃） |
| Stability: | Stable. Substances to be avoided include strong oxidizing agents. Combustible. |
| Major Application | pharmaceutical (small molecule) |
| Cosmetics Ingredients Functions | PERFUMING SOLVENT ANTIMICROBIAL |
| Cosmetic Ingredient Review (CIR) | Benzyl benzoate (120-51-4) |
| InChI | 1S/C14H12O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H2 |
| InChIKey | SESFRYSPDFLNCH-UHFFFAOYSA-N |
| SMILES | O=C(OCc1ccccc1)c2ccccc2 |
| LogP | 4 at 20℃ |
| Surface tension | 45.95mN/m at 20°C |
| CAS DataBase Reference | 120-51-4(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzyl Benzoate(120-51-4) |
| EPA Substance Registry System | Benzyl benzoate (120-51-4) |
Safety Information
| Hazard Codes | Xn,N |
| Risk Statements | 22-51/53 |
| Safety Statements | 25-61-46 |
| RIDADR | UN 3082 9 / PGIII |
| WGK Germany | 2 |
| RTECS | DG4200000 |
| Autoignition Temperature | 896 °F |
| TSCA | TSCA listed |
| HazardClass | 9 |
| HS Code | 29163100 |
| Storage Class | 10 - Combustible liquids |
| Hazard Classifications | Acute Tox. 4 Oral Aquatic Acute 1 Aquatic Chronic 2 |
| Hazardous Substances Data | 120-51-4(Hazardous Substances Data) |
| Toxicity | LD50 in rats, mice, rabbits, guinea pigs (g/kg): 1.7, 1.4, 1.8, 1.0 orally (Draize) |
| Description | Benzyl benzoate (BnBzO) is a mediation and insect repellent. It is one of the older preparation used to treat scabies which is a skin infections caused by the mite scarcoptes scabiei since it is lethal to the mite. It is capable of killing the mite in 5 minutes. It can also be used for the treatment of lice infestation of the head and the body. Its mechanism of action is through exerting toxic effect on the nervous system of the insects, further causing its death. It is also toxic to mite ova through an unknown mechanism. It can also be used as a repellent for chiggers, ticks, and mosquitoes as well as a dye carrier, solvent of cellulose derivatives, plasticizer, and a fixative. |
| Chemical Properties | Benzyl benzoate is a clear, colorless, oily liquid with a light, balsamic odor reminiscent of almond and a sharp, pungent taste. It produces a sharp, burning sensation on the tongue. At temperatures below 178℃ it exists as clear, colorless crystals. |
| Uses | Benzyl Benzoate has seen use as an insecticide, as well as a solvent for various chemical reactions. Benzyl benzoate is a benzyl compound that can be synthesized by reacting benzyl chloride with sodium benzoate in the presence of tetrabutylaramonium iodide. It has been used to: Prepare benzyl alcohol/benzyl benzoate (BABB) solution employed for enhancing the tissue transparency during the whole-mount immunostaining BABB method. Study its ability to induce an olfactory response in the third instar larvae of Drosophila melanogaster. Prepare Spalteholz fluid in combination with methyl salicylate, employed during LSFM (light sheet fluorescence microscopy) imaging. |
| Preparation | Benzyl benzoate is a constituent of Peru balsam and occurs naturally in certain plant species. Commercially, benzyl benzoate is produced synthetically by the dry esterification of sodium benzoate and benzoyl chloride in the presence of triethylamine or by the reaction of sodium benzylate with benzaldehyde. |
| toxicity | In man, benzyl benzoate was a skin sensitizer and caused gastro-intestinal effects in an infant. It was of moderate to low acute oral toxicity in a range of laboratory animal species and of low acute dermal toxicity in rabbits. Central nervous system effects were induced in several species given single doses orally or dermally. Repeated skin applications caused degenerative changes in various organs (including the liver, spleen and testes) of rabbits. No effects were seen in reproductive studies involving repeated oral administration to rats during pregnancy and lactation. Benzyl benzoate gave no evidence of mutagenicity in an Ames bacterial assay. It was a mild skin irritant in rabbits. |
| References | https://www.drugbank.ca/drugs/DB00676 https://en.wikipedia.org/wiki/Benzyl_benzoate |
| Description | Benzyl benzoate is the ester of benzyl alcohol and benzoic acid, with the formula C6H5CH2O2CC6H5. This easily prepared compound with a mild balsamic odor has a variety of uses.Benzyl benzoate (BB) is one of the oldest drugs used for the treatment of scabies and is recommended as the “first-line intervention” for the cost-effective treatment of the disease. |
| Chemical Properties | Benzyl Benzoate is the main component of Peru balsam oil. It occurs in fairly large amounts in a number of blossom concretes and absolutes (e.g., tuberose and hyacinth). It forms either a viscous liquid or solid flakes (mp 21–22°C) and has a weak, sweet, balsamic odor. Benzyl Benzoate is prepared either by transesterification of technical methyl benzoate with benzyl alcohol or from benzyl chloride and sodium benzoate. A third process starts with benzaldehyde, which is converted in high yield into benzyl benzoate in the presence of sodium or aluminum benzylate (Tishchenko reaction). Benzyl benzoate is used in perfumery as a fixative and as a modifier in heavy blossom fragrances. |
| Occurrence | Contained in Peru balsam and in the concrete and absolute of tuberose flowers, hyacinth, Narcissus jonquillaL., and Dianthus caryophillus L.; also in the oil of ylang-ylang and in Tolu balsam. Reported found in American cranberry, cinnamonbark, cassia leaf, corn oil and hog plum (Spondias mombins L.). |
| Uses | Benzyl benzoate, as a topical solution, may be used as an antiparasitic insecticide to kill the mites responsible for the skin condition scabies , for example as a combination drug of benzyl benzoate/disulfiram. It has other uses : a fixative in fragrances to improve the stability and other characteristics of the main ingredients a food additive in artificial flavors a plasticizer in cellulose and other polymers a solvent for various chemical reactions a treatment for sweet itch in horses a treatment for scaly leg mites in chickens. |
| Uses | benzyl benzoate is an anti-microbial. It can also act as a solvent, helping dissolve other substances in the product, and as a perfuming ingredient. It is the ester of benzyl alcohol and benzoic acid. |
| Uses | As solvent of cellulose acetate, nitrocellulose and artificial musk; substitute for camphor in celluloid and plastic pyroxylin Compounds; perfume fixative; in confectionery and chewing gum flavors. |
| Preparation | By the dry esterification of sodium benzoate and benzoyl chloride in the presence of triethylamine or by reaction ofsodium benzylate on benzaldehyde. |
| Production Methods | BENZYL BENZOATE is produced by the Cannizzaro reaction from benzaldehyde, by esterifying benzyl alcohol with benzoic acid, or by treating sodium benzoate with benzyl chloride. It is purified by distillation and crystallization. Benzyl benzoate is used as a fixative and solvent for musk in perfumes and flavors, as a plasticizer, miticide, and in some external medications. The compound has been found effective in the treatment of scabies and pediculosis capitis (head lice, Pediculus humanus var. capitis). |
| Indications | Benzyl benzoate: 20% to 25%. This agent is relatively nontoxic and is widelyused in developing countries to treat scabies and pediculosis capitis and pubis.Only a veterinary preparation is available in the United States. Benzyl benzoate issynthetically derived from the esterification of benzoic acid with benzyl alcohol. Itsmechanism of action is unknown. It is toxic to Sarcoptes scabei and may be toxicto Pediculosis capitis and Phthirus pubis. No resistance has been demonstratedto date. Benzyl benzoate can be used in a 5% emulsion to repel many arthropods and canbe used as a lotion to treat sarcoptic mange and canine pediculosis. |
| Definition | ChEBI: Benzyl benzoate is a benzoate ester obtained by the formal condensation of benzoic acid with benzyl alcohol. It has been isolated from the plant species of the genus Polyalthia. It has a role as a scabicide, an acaricide and a plant metabolite. It is a benzyl ester and a benzoate ester. It is functionally related to a benzoic acid. |
| Definition | Benzyl benzoate is produced from benzyl alcohol and sodium benzoate in the presence of triethylamine or by transesterification of methyl benzoate with benzyl alcohol in the presence of an alkali benzyl oxide. In another manufacturing process benzaldehyde is condensed to form benzyl benzoate in the presence of sodium (Claisen-Tishchenko condensation). The presence of a small amount of an aliphatic ether improves this reaction. Benzyl benzoate is a byproduct in the manufacture of benzoic acid by the oxidation of toluene; it is present in the benzoic acid distillation residue. |
| Brand name | Pharmaceutic necessity forDimercaprol [Injection]. Benylate (Sterling Winthrop). |
| Taste threshold values | Taste characteristics at 30 ppm: balsamic, fruity with powdery and berry nuances. |
| Synthesis Reference(s) | Journal of Heterocyclic Chemistry, 24, p. 187, 1987 DOI: 10.1002/jhet.5570240135 Tetrahedron Letters, 27, p. 2383, 1986 DOI: 10.1016/S0040-4039(00)84535-9 |
| General Description | Benzyl benzoate is an aromatic ester that is used as a food flavoring agent. It has been identified as one of the main volatile aroma component of cranberry, mango and Egyptian Jasminum sambac flowers. |
| Hazard | Irritant to eyes, skin. |
| Flammability and Explosibility | Not classified |
| Pharmaceutical Applications | Benzyl benzoate is used as a solubilizing agent and nonaqueoussolvent in intramuscular injections at concentrations of0.01–46.0% v/v, and as a solvent and plasticizer for celluloseand nitrocellulose. It is also used in the preparation of spray-driedpowders using nanocapsules. However, the most widespread pharmaceutical use of benzylbenzoate is as a topical therapeutic agent in the treatment ofscabies. Benzyl benzoate is also used therapeutically as aparasiticide in veterinary medicine. Other applications of benzyl benzoate include its use as apediculicide, and as a solvent and fixative for flavors and perfumesin cosmetics and food products. |
| Contact allergens | Benzyl benzoate is the ester of benzyl alcohol andbenzoic acid. It is contained in Myroxylon pereiraeand Tolu balsam. It is used in acaricide preparationsagainst Sarcoptes scabiei or as a pediculicide. Directcontact may cause skin irritation, but rarely allergiccontact dermatitis. As a fragrance allergen, benzylbenzoate has to be mentioned by name in EUcosmetics. |
| Biochem/physiol Actions | Benzyl benzoate is the condensation product of benzoic acid and benzyl alcohol. It is utilized for treating human scabies as well as kills house dust mite. |
| Clinical Use | Benzyl benzoate is a naturally occurring ester obtained fromPeru balsam and other resins. It is also prepared syntheticallyfrom benzyl alcohol and benzoyl chloride. The ester isa clear colorless liquid with a faint aromatic odor. It is insolublein water but soluble in organic solvents. Benzyl benzoate is an effective scabicide when appliedtopically. Immediate relief from itching probably resultsfrom a local anesthetic effect; however, a complete cureis frequently achieved with a single application of a 25%emulsion of benzyl benzoate in oleic acid, stabilized withtriethanolamine. This preparation has the additionaladvantage of being essentially odorless, nonstaining, andnonirritating to the skin. It is applied topically as a lotionover the entire dampened body, except the face. |
| Safety | Benzyl benzoate is metabolized by rapid hydrolysis to benzoic acidand benzyl alcohol. Benzyl alcohol is then further metabolized tohippuric acid, which is excreted in the urine. Benzyl benzoate is widely used as a 25% v/v topical applicationin the treatment of scabies and as an excipient in intramuscularinjections and oral products. Adverse reactions to benzyl benzoateinclude skin irritation and hypersensitivity reactions. Oral ingestionmay cause harmful stimulation of the CNS and convulsions. Benzylbenzoate should be avoided by perople with perfume allergy. LD50 (cat, oral): 2.24 g/kg LD50 (dog, oral): 22.44 g/kg LD50 (guinea pig, oral): 1.0 g/kg LD50 (mouse, oral): 1.4 g/kg LD50 (rabbit, oral): 1.68 g/kg LD50 (rabbit, skin): 4.0 g/kg LD50 (rat, oral): 0.5 g/kg LD50 (rat, skin): 4.0 g/kg |
| Synthesis | This colorless liquid is formally the condensation product of benzoic acid and benzyl alcohol. It can also be generated from benzaldehyde by the Tishchenko reaction. |
| Environmental Fate | Benzyl benzoate acts as a local irritant. At high levels of exposure,free benzoic acid may sequester significant amounts ofacetyl coenzyme A (CoA), which could disrupt cholinergicsignaling. Recent findings suggest that benzyl benzoate mayhave estrogenic properties. |
| Metabolism | Benzyl benzoate, a relatively non-toxic liquid widely used for the treatment of scabies, is converted into benzoic acid in vivo (Williams, 1959). |
| storage | Benzyl benzoate is stable when stored in tight, well-filled, lightresistantcontainers. Exposure to excessive heat (above 408℃)should be avoided. |
| Toxicity evaluation | Acute oral LD50 for rats: 1,700 mg/kg |
| Incompatibilities | Benzyl benzoate is incompatible with alkalis and oxidizing agents. |
| Regulatory Status | Included in the FDA Inactive Ingredients Database (IM injectionsand oral capsules). Included, as an active ingredient, in nonparenteralmedicines licensed in the UK. Included in the Canadian Listof Acceptable Non-medicinal Ingredients. |
Benzyl benzoate Preparation Products And Raw materials
| Raw materials | Sodium-->Sodium carbonate-->Triethylamine-->Benzaldehyde-->Benzyl alcohol-->Benzoic acid-->Sodium benzoate-->Ethyl benzoate-->Peru balsam |
| Preparation Products | 3-Phenoxybenzyl alcohol-->2,6-Dichloroaniline-->4-Cyanophenol-->Batyl alcohol-->Butethamine-->Disperse Yellow 126-->Benzyl ether-->PENTYL VALERATE-->Hexyl benzoate-->2,4,6-Trimethylbenzophenone-->Isobutyl isobutyrate |
