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beta-Bromostyrene

HCID 7667
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Basic information

CAS
103-64-0
Standard SMILES
BrC=Cc1ccccc1
InChIKey
YMOONIIMQBGTDU-UHFFFAOYSA-N
Molecular formula
C8H7Br
Average molar mass
183.04 g/mol
Monoisotopic mass
181.97311232

Names & identifiers

Preferred name
beta-Bromostyrene
IUPAC
2-bromoethenylbenzene
English name
beta-Bromostyrene
Molecular formula
C8H7Br
Molecular weight
183.05

Names & synonyms

BETA-BROMOSTYRENEStyryl bromideDTXSID501014586beta-BromstyrolStyrene, beta-bromo-1-Bromo-2-phenylethenealpha-Bromo-beta-phenylethylene46J0U1IRC9NSC-8047omega-BromostyreneL50CQ41322RefChem:819270
Show more names
β-Bromostyrene[(E)-2-Bromoethenyl]benzene1-BROMO-2-PHENYLETHYLENE(Z)-β-bromostyreneBROMSTYROLBromstyroleB-BROMSTYROLhyacinthbasestyrylbromide
DTXCID5034149203-131-3(2-Bromoethenyl)benzene(2-Bromovinyl)benzene103-64-0Benzene, (2-bromoethenyl)-BromostyrolBromostyrolene

Database identifiers

CAS
103-64-0、1335-06-4
PubChem CID
7667
DTXSID
DTXSID501014586
EC Number
203-131-3、215-617-2

Properties

Computed structural propertiesFilling in

XLogP
2.9
Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
1
Heavy atoms
9
Formal charge
0
Complexity
90.7

Experimental & physicochemical properties

Chemical ClassesOther Classes -> Halogenated Monoaromatics
SpringerMaterials PropertiesDensity
FragrancesFragrance substance (Bromostyrene) -> IFRA amendment 43
Odor · 2 items

Strong Hyacinth odor

Strong floral odor

Density1.395-1.424
Color/Form · 2 items

Pale yellow oil.

Yellowish liquid

Solubility · 3 items

Insol in aqueous solution

Miscible with alcohol, ether

Sol in 4 volumes of 90% alcohol

Flash Point79 °C (closed cup)
Boiling Point112 °C at 20 mm Hg
DecompositionWhen heated to decomposition it emits toxic fumes of /hydrogen bromide/.

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

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

Hazard information

Regulatory Information · 3 items

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

Hazards SummaryOral LD50 (rat) = 1250 mg/kg; [RTECS] May cause irritation; [MSDSonline]
Toxic Combustion ProductsWhen heated to decomposition, it emits toxic fumes of /hydrogen bromide/.
Hazard Classes and Categories · 3 items

Acute Tox. 4 (100%)

Not Classified

Flammable liquids - Category 4

Safety & protection

Disposal Methods · 1 item

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.

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 2 items

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.

Uses & manufacturing

Uses · 3 items

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

Consumption PatternsUse in fragrances in the USA amounts to less than 1000 lb/yr.
IFRA Fragrance Standards · 6 items

Bromostyrene

Benzene, (2-bromoethenyl)-; α-Bromo-ß-phenylethylene; ß-Bromostyrene; ß-Bromovinylbenzene; ω-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

Related reactions

20 records
New reaction record
HRID 173853 reaction equation
HRID 173853As reactantTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
HRID 238358 reaction equation
HRID 238358As reactantuspto-grants-2014_02
HRID 259389 reaction equation
HRID 259389As reactantuspto-grants-1977_07
HRID 497577 reaction equation
HRID 497577As reactantuspto-grants-2005_09
HRID 1105534 reaction equation
HRID 1105534As reactantuspto-grants-1982_01
HRID 1350391 reaction equation
HRID 1350391As reactantuspto-grants-2007_05
HRID 1400399 reaction equation
HRID 1400399As reactantuspto-grants-2014_12
HRID 1400560 reaction equation
HRID 1400560As reactantuspto-grants-2014_12
Page 1 of 3

Compound notes

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Melting Pointmin, - 2 °C
Vapor Pressure0.12 [mmHg]

Physicochemical properties

Melting point
7 °C · 7 °C(lit.)
Boiling point
219 · 219-221 °C(lit.)
Density
1.427 g/mL · 1.427 g/mL at 25 °C(lit.)
vapor pressure
16.4 Pa · 16.4Pa at 25℃
refractive index
20 · n20/D 1.608
Flash point
215 °F · 215 °F
storage temp.
2 · 2-8°C
solubility
Soluble in alcohol.
form
Liquid
color
very deep green-yellow
Odor
1 % · at 1.00 % in dipropylene glycol. strong leafy green hyacinth
Odor Type
green
Water Solubility
56.624 mg/L · 56.624mg/L at 25℃
BRN
2038495 · 2038495
Henry's Law Constant
1.8 · 1.8×10-2 mol/(m3Pa) at 25℃, HSDB (2015)
InChI
1S/C8H7Br/c9-7-6-8-4-2-1-3-5-8/h1-7H/b7-6+
InChIKey
YMOONIIMQBGTDU-VOTSOKGWSA-N
SMILES
Br\C=C\c1ccccc1
LogP
3.391 at · 3.391 at 25℃
CAS DataBase Reference
103 · 103-64-0(CAS DataBase Reference)
EWG's Food Scores
1 · 1-3
FDA UNII
46 J0U1IRC9 · 46J0U1IRC9
NIST Chemistry Reference
Benzene, (2-bromoethenyl)-(103-64-0)
EPA Substance Registry System
.beta.-Bromostyrene (103-64-0)
UNSPSC Code
12352100 · 12352100
NACRES
22 · NA.22
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302-H227
Precautionary statements
264 · P264-P270-P301+P312+P330-P501-P210e-P280a-P301+P312a-P403+P235-P501a
PPE
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes
Xn
Risk Statements
22 · 22
Safety Statements
23 · 23-24/25-36/37
WGK Germany
3 · 3
RTECS
3850000 · WL3850000
TSCA
TSCA listed
HS Code
29039990 · 29039990
Storage Class
10 · 10 - Combustible liquids
Hazard Classifications
4 Oral · Acute Tox. 4 Oral
Hazardous Substances Data
103 · 103-64-0(Hazardous Substances Data)
Toxicity
50 in · An acute oral LD50 in rats was reported as 1.25 ml/kg(0.82-189 ml/kg). The acute dermal LD50 was reported as > 6 ml/kg in the rabbit
REACH Registrations
Inactive

Toxicology

Environmental Fate · 3 items

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).

Soil Adsorption/Mobility · 1 item

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).

Natural Pollution SourcesHas not been reported to occur in nature.
Human Toxicity ExcerptsBromostyrol tested at a concn of 4% in petrolatum produced no irritation /or sensitization reactions/ in a 48 hr closed-patch test in 25 human subjects. ... /It/ is one of the strongly irritant perfume materials.
Artificial Pollution Sourcesbeta-Bromostyrene's production and in use as a food additive(1) and fragrance in consumer products(2) may result in its release to the environment through various waste streams(SRC).
Environmental BiodegradationData regarding the biodegradation of beta-bromostyrene in either soil or aquatic systems were not available. (SRC)
Environmental Bioconcentration · 1 item

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).

Volatilization from Water/Soil · 1 item

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).

Non-Human Toxicity ExcerptsADMINISTRATION OF BETA-BROMOSTYRENE TO RATS RESULTS IN FALL IN LEVEL OF HEPATIC GLUTATHIONE.
Environmental Abiotic Degradation · 1 item

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).

Probable Routes of Human Exposure · 1 item

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).

Environmental Fate/Exposure Summary · 1 item

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)

Safety data

PPE
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
wgk
3
tsca
TSCA listed
rtecs
WL3850000
hs_code
29039990
Toxicity
An acute oral LD50 in rats was reported as 1.25 ml/kg(0.82-189 ml/kg). The acute dermal LD50 was reported as > 6 ml/kg in the rabbit
risk_code
22
Signal word
Warning
Symbol(GHS)
GHS07
hazard_code
Xn
safety_code
23-24/25-36/37
Storage Class
10 - Combustible liquids
Hazard statements
H302-H227
REACH Registrations
Inactive
Hazard Classifications
Acute Tox. 4 Oral
Precautionary statements
P264-P270-P301+P312+P330-P501-P210e-P280a-P301+P312a-P403+P235-P501a
Hazardous Substances Data
103-64-0(Hazardous Substances Data)
Methods of Manufacturing · 2 items

Preparation is by the action of aqueous alkali on cinnamic acid bromide.

Cinnamic acid + bromine (addition/dehydrobromination/decarboxylation)

General Manufacturing Information · 3 items

Benzene, (2-bromoethenyl)-: ACTIVE

Benzene, bromoethenyl-: ACTIVE

/Has been available for/ public use since the 1920s.

Applications · 5 items

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.

Preparation methods

PreparationBy the action of aqueous alkali on cinnamic acid dibromide.

Upstream & downstream products

Upstream raw materials

Cinnamyl bromidealpha-Bromostyrene3-Butyn-1-ol

Downstream products

PhenylacetyleneIsoamylbenzeneCINNAMONITRILE