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103-64-0BrC=Cc1ccccc1YMOONIIMQBGTDU-UHFFFAOYSA-N103-64-0、1335-06-4DTXSID501014586Strong Hyacinth odor
Strong floral odor
Pale yellow oil.
Yellowish liquid
Insol in aqueous solution
Miscible with alcohol, ether
Sol in 4 volumes of 90% alcohol
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
Warning
H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 139 reports by companies from 2 notifications to the ECHA C&L Inventory.
This chemical does not meet GHS hazard criteria for 100% (16 of 16) of all reports.
Not Classified
Chemical: Benzene, (2-bromoethenyl)-
Status: Cease Manufacture Update: 18-01-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/17758
beta-Bromostyrene: Does not have an individual approval but may be used under an appropriate group standard
Acute Tox. 4 (100%)
Not Classified
Flammable liquids - Category 4
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
THE ADMINISTRATION OF BETA-BROMOSTYRENE (A FOOD ADDITIVE) TO THE RAT RESULTS IN A FALL IN THE LEVEL OF HEPATIC GLUTATHIONE. MARMOSETS, RABBITS AND RATS DOSED WITH BETA-BROMOSTYRENE EXCRETE TWO MERCAPTURIC ACIDS. ONE OF THESE, N-ACETYL-S-(2-HYDROXY-2-PHENYL-1-BROMOETHYL)-CYSTEINE IS READILY CONVERTED INTO N-ACETYL-S-(1-PHENYL-2-BROMO-2-ETHENYL)-CYSTEINE, THE STRUCTURE OF WHICH WAS ESTABLISHED BY MASS SPECTROMETRY. MASS SPECTROMETRIC EVIDENCE SUGGESTS THAT THE 2ND MERCAPTURIC ACID WAS N-ACETYL-S-(1-HYDROXY-2-PHENYLETHYL)CYSTEINE. MANDELIC ACID WAS DETECTED AS A METABOLITE IN ALL 3 SPECIES.
The reaction products of deoxyguanosine with 3,4-dimethyl-, p-methyl-, m-methyl-, m-ethoxy-, p-bromo-, m-chloro- and unsubstituted styrene oxide were isolated and characterized. The reaction followed second order kinetics. The reactive site was the N-7 site of guanine. The normal isomer (attack at CH2 of styrene oxides) and the abnormal isomer (attack at CH) were obtained. The Hammett reaction constant (rho) for the normal reaction was +0.42 and that for the abnormal reactlon was -1.1. The difference of acid dissociation constant, rate of imidazole ring opening and rate of glycosidic bond cleavage was not found between the normal adduct and the abnormal adduct.
Used as a food additive and as a fragrance in soaps, detergents, creams, lotions, and perfumes; [HSDB]
A food additive
Used in fragrances in the USA include soap, detergent, creams, lotions, & perfume
Bromostyrene
Benzene, (2-bromoethenyl)-; α-Bromo-Ã-phenylethylene; Ã-Bromostyrene; Ã-Bromovinylbenzene; Ï-Bromstyrene; Bromstyrol; Bromstyrolene
IFRA_STD_117.pdf
43
IFRA 51st Amendment - Guidance for the use of IFRA Standards
Prohibition: This material should not be used as a fragrance ingredient
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TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 960(SRC), determined from a structure estimation method(2), indicates that beta- bromostyrene is expected to have low mobility in soil(SRC). Volatilization of beta-bromostyrene from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.5X10-4 atm-cu m/mole(SRC), using a fragment constant estimation method(3). beta-Bromostyrene is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 0.12 mm Hg(SRC), determined from a fragment constant method(4).
AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 960(SRC), determined from a structure estimation method(2), indicates that beta-bromostyrene is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 5.5X10-4 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 6 hrs and 6 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 3(SRC), from an estimated log Kow of 3.15(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), beta-bromostyrene, which has an estimated vapor pressure of 0.12 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely as a vapor in the ambient atmosphere(SRC). Vapor-phase beta-bromostyrene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals and ozone(SRC); the half-lives for these reactions in air are estimated to be 22 hrs and 6 days, respectively(SRC), calculated from rate constants of 1.7X10-11 cu cm/molecule-sec and 2.2X10-18 cu cm/molecule-sec (cis- and trans- avg), respectively, at 25 °C(SRC) and derived using a structure estimation method(3).
Using a structure estimation method based on molecular connectivity indices(1), the Koc for beta-bromostyrene can be estimated to be 960(SRC). According to a classification scheme(2), this estimated Koc value suggests that beta-bromostyrene is expected to have low mobility in soil(SRC).
An estimated BCF of 3 was calculated for beta-bromostyrene(SRC), using an estimated log Kow of 3.15(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Henry's Law constant for beta-bromostyrene is estimated as 5.5X10-4 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that beta-bromostyrene is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 6 hrs(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 6 days(SRC). beta-Bromostyrene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). beta-Bromostyrene is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 0.12 mm Hg(SRC), determined from a fragment constant method(3).
The rate constant for the vapor-phase reaction of beta-bromostyrene with photochemically-produced hydroxyl radicals has been estimated as 1.7X10-11 cu cm/molecule-sec (cis- and trans- avg) at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 22 hrs an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). The rate constant for the vapor-phase reaction of beta-bromostyrene with ozone has been estimated as 2.2X10-18 cu cm/molecule-sec (cis- and trans- avg) at 25 °C(SRC) that was derived using a structure estimation method(1). This corresponds to an atmospheric half-life of about 6 days at an atmospheric concentration of 7X10+11 ozone molecules per cu cm(2). beta-Bromostyrene is not expected to undergo hydrolysis in the environment due to the lack of hydrolysis of vinyl bromides(3).
NIOSH (NOES Survey 1981-1983) has statistically estimated that 20,488 workers (12,772 of these are female) are potentially exposed to beta-bromostyrene in the US(1). Occupational exposure to beta-bromostyrene may occur through dermal contact with this compound at workplaces where beta-bromostyrene is produced or used(SRC). The general population may be exposed to beta-bromostyrene via dermal contact with consumer products(2) containing beta-bromostyrene(SRC).
beta-Bromostyrene's production and in use as a food additive and fragrance in consumer products may result in its release to the environment through various waste streams. If released to air, an estimated vapor pressure of 0.12 mm Hg at 25 °C indicates beta-bromostyrene will exist solely as a vapor in the ambient atmosphere. Vapor-phase beta-bromostyrene will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals and ozone; the half-lives for these reactions in air are estimated to be 22 hrs and 6 days, respectively. If released to soil, beta-bromostyrene is expected to have low mobility based upon an estimated Koc of 960. Volatilization from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 5.5X10-4 atm-cu m/mole. If released into water, beta-bromostyrene is expected to adsorb to suspended solids and sediment based upon the estimated Koc. Volatilization from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 6 hrs and 6 days, respectively. An estimated BCF of 3 suggests the potential for bioconcentration in aquatic organisms is low. Hydrolysis is not expected to occur due to the lack of hydrolysis of vinyl bromides. Occupational exposure to beta-bromostyrene may occur through dermal contact with this compound at workplaces where beta-bromostyrene is produced or used. The general population may be exposed to beta-bromostyrene via dermal contact with consumer products containing beta-bromostyrene. (SRC)
Preparation is by the action of aqueous alkali on cinnamic acid bromide.
Cinnamic acid + bromine (addition/dehydrobromination/decarboxylation)
Benzene, (2-bromoethenyl)-: ACTIVE
Benzene, bromoethenyl-: ACTIVE
/Has been available for/ public use since the 1920s.
OccurrenceApparently has not been reported to occur in nature.
UsesPerfumery.
UsesBeta-Bromostyrene, cis + trans is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
Usesβ-Bromostyrene was used in the one-pot method for the preparation of cinnamonitriles. It was also used in the preparation of pure ethyl Z- and E-α,α-difluoro-4-phenyl-3-butenoate and 1,3-diphenyl-1-butene. It may be used in the synthesis of β-tert-butylstyrene via cross coupling reaction with tert-butylmagnesium chloride in the presence of dichloro[1,1′-bis(diphenylphosphino)ferrocene]nickel(II) catalyst. It may also be used to prepare γ-but-2-enolactone by reacting with nickel carbonyl in the presence of alkynes.
General Descriptionβ-Bromostyrene is an α,β-unsaturated aromatic halide. It can be synthesized by catalytic Hunsdiecker reaction (CHR) of cinnamic acid. It is commonly utilized as a precursor for preparing substituted alkenes, corresponding acetylenes and also in the total synthesis of natural compounds and antibiotics.
PreparationBy the action of aqueous alkali on cinnamic acid dibromide.