Allylbromid

Allyl bromide

HCID 7841CAS 106-95-6

Grundinformationen

Standard-SMILES
C=CCBr
InChIKey
BHELZAPQIKSEDF-UHFFFAOYSA-N
Summenformel
C3H5Br
Durchschnittliche Molmasse
120,98 g/mol
Monoisotopische Masse
119,95746226

Überblick

Allyl bromide appears as a clear colorless to light yellow liquid with an irritating unpleasant odor. Flash point 30 °F. Irritates eyes, skin, and respiratory system. Toxic by skin absorption. Denser than water and slightly soluble in water.

Namen und Bezeichner

Bevorzugter Name
Allyl bromide
IUPAC
3-bromoprop-1-ene
Lokaler Name
Allylbromid
Englischer Name
Allyl bromide
Summenformel
C3H5Br
Molmasse
120.98

Namen und Synonyme

ALLYL BROMIDE106-95-63-bromoprop-1-ene3-Bromopropene3-Bromo-1-propene1-Propene, 3-bromo-3-Bromopropylene2-Propenyl bromideBromallylene1-Bromo-2-propenePropene, 3-bromo-DTXSID8024442
Weitere Namen anzeigen
3-bromopropaneAllylbromid3-Brompropen3-bromo-prop-1-eneCH2=CHCH2Br
FXQ8X2F74ZNSC-7596DTXCID204442RefChem:5525203-446-6allylbromideNSC 7596MFCD00000244

Datenbank-Bezeichner

CAS
106-95-6
PubChem CID
7841
DTXSID
DTXSID8024442
ChEMBL
CHEMBL1429506
UNII
FXQ8X2F74Z
EC Number
203-446-6
Nikkaji
J4.040A

Eigenschaften

Berechnete Struktureigenschaften

XLogP
1,8
Polarare Oberfläche (TPSA)
0 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
0
Frei drehbare Bindungen
1
Schwere Atome
4

Experimentelle und physikochemische Eigenschaften

Chemical Classes · 2 Einträge

Other Classes -> Halogenated Aliphatics, Unsaturated

Flammable agents - 3rd degree

SpringerMaterials PropertiesSchoenflies notation
LogP · 2 Einträge

log Kow = 1.79

1.9

OdorUnpleasant, pungent
Density · 3 Einträge

1.4161 at 68 °F (USCG, 1999) - Denser than water; will sink

1.398 at 20 °C/4 °C

1.3980 @ 20°C

Color/FormColorless to light yellow liquid

Physikochemische Eigenschaften

Schmelzpunkt
-119 °C · -119 °C
Siedepunkt
70 · 70-71 °C(lit.)
Dichte
1.398 g/mL · 1.398 g/mL at 25 °C(lit.)
Dampfdichte
4.2 · 4.2 (vs air)
Dampfdruck
18.66 kPa · 18.66kPa at 25℃
Brechungsindex
20 · n20/D 1.469(lit.)

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H225 (92.6%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P203, P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P264+P265, P270, P271, P273, P280, P284, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P316, P318, P319, P320, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P363, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 68 reports by companies from 18 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H225: Highly Flammable liquid and vapor [Danger Flammable liquids]

Gefahrenhinweise

Regulatory Information · 5 Einträge

Chemical: 1-Propene, 3-bromo-

1-Propene, 3-bromo- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1-Propene, 3-bromo- 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)

Status: Active Update: 18-06-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/10333

3-Bromo-1-propene: HSNO Approval: HSR004256 Approved with controls

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelFlammable Liquid Poison
Fire Hazards · 2 Einträge

Special Hazards of Combustion Products: Toxic hydrogen bromide and bromine gases formed in fire.

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Fire PotentialDangerous fire and explosion hazard when exposed to heat or flame.
Health Hazards · 2 Einträge

Inhalation of vapor irritates mucous membranes and causes dizziness, headache, and lung irritation. Contact with liquid irritates eyes and skin. Ingestion causes irritation of mouth and stomach. (USCG, 1999)

· TOXIC; may be fatal if inhaled, ingested or absorbed through skin.

Hazards Summary · 1 Eintrag

A skin, eye, and respiratory tract irritant; May cause severe burns to skin and eyes; May be mutagenic; [HSDB] May polymerize; A strong reducing agent; A skin, eye, and respiratory tract irritant; [CAMEO] No evidence of carcinogenic activity in mice fed up to 8 mg/kg by corn oil gavage 5 days a week for 40 weeks; [NTP] TLV basis is eye and upper respiratory tract irritant; [ACGIH] A lachrymator; [CHEMINFO]

Sicherheit und Schutzausrüstung

Fire FightingExcerpt from ERG Guide 131 [Flammable Liquids - Toxic; polymerization hazard]:
Accidental Release Measures · 2 Einträge

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 2 Einträge

INHALATION: remove from exposure; if not breathing, give artificial respiration; if breathing is difficult, give oxygen; call physician.

General First Aid:

Firefighting HazardsVapors are heavier than air and may travel to a source of ignition and flash back.
Exposure Control and Personal Protection · 2 Einträge

· Wear positive pressure self-contained breathing apparatus (SCBA).

257.0 [ppm]

Fire Fighting Procedures · 4 Einträge

Water may be ineffective.

Use dry chemical, foam, carbon dioxide, or water spray. Water may be ineffective. Use water spray to keep fire-exposed containers cool. Approach fire from upwind to avoid hazardous vapors and toxic decomp products.

If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped or safely confined. 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 "alcohol" foam, dry chemical or carbon dioxide.

Evacuation: If fire becomes uncontrollable or container is exposed to direct flame - consider evacuation of one-third (1/3) mile radius.

Toxikologische Informationen

Treatment · 1 Eintrag

EYES: irrigate opened eyes for several minutes under running water. INGESTION: do not induce vomiting. Rinse mouth with water (never give anything by mouth to an unconscious person). Seek immediate medical advice. SKIN: should be treated immediately by rinsing the affected parts in cold running water for at least 15 minutes, followed by thorough washing with soap and water. If necessary, the person should shower and change contaminated clothing and shoes, and then must seek medical attention. INHALATION: supply fresh air. If required provide artificial respiration.

Interactions · 1 Eintrag

In rats, cysteine magnesium nitrate and cysteine magnesium acetate administration ip resulted in 17-33% higher survival rate following allyl bromide poisoning than did cysteine administration. Cysteine magnesium bromide was as effective as cysteine against allyl bromide poisoning.

Health Effects · 1 Eintrag

Acute poisoning of laboratory animals is accompanied by a transient motor agitation followed by depression and loss of balance. Death occurs within 24 hours. Allyl bromide is considered as one of the most toxic of the halogenated hydrocarbons, causing deaths in experimental animals exposed for 4 hr to concentrations as low as 1 mg/L. It is mutagenic but there is no evidence that it is carcinogenic. Target organs are gastrointestinal system, eyes, skin, respiratory system.

Ecotoxicity Values · 2 Einträge

LC50 Carassius auratus (Goldfish) <800 ug/L/24 hr; static

LC50 Xenopus laevis (Clawed toad) 660 ug/L/48 hr; static /formulated product/

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 230(SRC), determined from a log Kow of 1.79(2) and a regression-derived equation(3), indicates that allyl bromide is expected to have moderate mobility in soil(SRC). Volatilization of allyl bromide from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.1X10-2 atm-cu m/mole(SRC), using a fragment constant estimation method(4). Allyl bromide is expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 140 mm Hg(SRC), determined from a fragment constant method(5). Based on BOD values of 56 and 74% in 5 days using sewage sludge(6), biodegradation may be an important environmental fate process in soil(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 230(SRC), determined from a log Kow of 1.79(2) and a regression-derived equation(3), indicates that allyl bromide is not 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 1.1X10-2 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 3 hours and 4 days, respectively(SRC). According to a classification scheme(5), an estimated BCF of 5(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Based on BOD values of 56 and 74% in 5 days using sewage sludge(8), biodegradation may be an important environmental fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), allyl bromide, which has an estimated vapor pressure of 140 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. Vapor-phase allyl bromide 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 20 hours(SRC), calculated from its rate constant of 2.0X10-11 cu cm/molecule-sec at 25 °C(SRC), that was derived using a structure estimation method(3). In addition, vapor-phase allyl bromide will react with ozone with a half-life of 7 days(SRC) calculated from an estimated rate constant of 1.5X10-16 cu cm/ molecule-sec(SRC), that was derived using a structure estimation method(3). Allyl bromide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsDermatotoxin - Skin burns.

Sicherheitsdaten

F
8-19
wgk
2
tsca
TSCA listed
ridadr
UN 1099
hs_code
29033036
RTECS-Nr.
UC7090000

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 5 Einträge

/Allyl bromide/...dosed sc to male rats /was/...metabolized into allylmercapturic acid, S-allylcysteine, and S-allylcysteine S-oxide. 3-Hydroxypropylmercapturic acid was /probably/ a metabolite...

S-Allyl-L-cysteine was isolated from urine of rats dosed with allyl bromide.

Urinary excretion of 3-hydroxypropylmercapturic acid (S-(3-hydroxypropyl)-N-acetyl-L-cysteine) following exposure to allylic compounds was studied in rats to examine the possibility of using 3-hydroxypropylmercapturic acid (S-(3-hydroxypropyl)-N-acetyl-L-cysteine) as a biological marker of exposure to allylic compounds that were metabolized to acrolein and excreted as 3-hydroxypropylmercapturic acid (S-(3-hydroxypropyl)-N-acetyl-L-cysteine) in the urine. Male Sprague Dawley rats were given ... 120 mg/kg allylbromide ... by gavage. Twenty four hour urine samples were collected for the next 48 hours and analyzed for 3-hydroxypropylmercapturic acid (S-(3-hydroxypropyl)-N-acetyl-L-cysteine) by HPLC. ... Total urinary excretion of 3-hydroxypropylmercapturic acid (S-(3-hydroxypropyl)-N-acetyl-L-cysteine) as a percentage of the dose ... averaged ... 3.0 percent for allylbromide ... .

Wistar rats were administered carbon 14 labeled ... allyl bromide ... orally. Urine, feces, exhaled carbon dioxide, and air were collected and analyzed for metabolites. The major metabolite found after treatment with ... allylbromide was S-carboxyethyl mercapturic acid.

Allyl bromide is metabolized into allylmercapturic acid, S-allylcysteine, and S-allylcysteine S-oxide and secreted in the urine. 3-Hydroxypropylmercapturic acid is also a metabolite.

Verwendung und Herstellung

Uses · 6 Einträge

Used to make perfumes, resins (copolymer with sulfur dioxide), fragrances, plastics, and dyestuffs; Also used as an insecticidal fumigant and contact poison; [HSDB]

Farming (Pesticides) [Category: Industry]

Manufacture of synthetic perfumes, other allyl compounds.

Insecticidal fumigant

Chemical intermediate in organic synthesis, for resins (copolymer with sulfur dioxide) and fragrances

As a fumigant (if quite volatile) or as a contact poison

U.S. Production · 3 Einträge

2023: 75,000 - <500,000 lb

(1998) > 10 thousand to 500 thousand pounds

(2002) > 10 thousand to 500 thousand pounds

Industry UsesUV stabilizer
Methods of Manufacturing · 2 Einträge

Reaction of hydrogen bromide and allyl alcohol; partial dehydrobromination of dibromopropane and separation of isomers.

Prepared from hydrobromic acid and allyl alcohol; ... from triphenylphosphite, allyl alcohol and benzyl bromide.

Formulations/Preparations · 2 Einträge

Grade: Technically pure (95% minimum purity by bromine titration).

Grades or Purity: Commercial

General Manufacturing Information · 2 Einträge

All Other Chemical Product and Preparation Manufacturing

1-Propene, 3-bromo-: ACTIVE

Anwendungen

BeschreibungDas 3-Brom-1-propen bildet eine farblose, wasserunlösliche Flüssigkeit. Die Verbindung findet vielfältige Anwendung bei organischen Synthesen.

Anbieter50 Anbieter

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