ChemicalBook > CAS DataBase List > Allyl bromide

Allyl bromide

Product Name
Allyl bromide
CAS No.
106-95-6
Chemical Name
Allyl bromide
Synonyms
3-BROMOPROPENE;3-BROMO-1-PROPENE;3-bromopropane;3-BROMOPROPYLENE;Allylbromid;BROMALLYLENE;3-Brompropen;3-bromo-prop-1-ene;CH2=CHCH2Br;ALLYL BROMIDE
CBNumber
CB7852691
Molecular Formula
C3H5Br
Formula Weight
120.98
MOL File
106-95-6.mol
More
Less

Allyl bromide Property

Melting point:
-119 °C
Boiling point:
70-71 °C(lit.)
Density 
1.398 g/mL at 25 °C(lit.)
vapor density 
4.2 (vs air)
vapor pressure 
18.66kPa at 25℃
refractive index 
n20/D 1.469(lit.)
Flash point:
28 °F
storage temp. 
2-8°C
solubility 
Chloroform (Soluble)
form 
Liquid
color 
Clear colorless to slightly colored
Specific Gravity
1.398
Odor
unpleasant
explosive limit
4.3-7.3%(V)
Water Solubility 
insoluble
Sensitive 
Light Sensitive
Merck 
14,288
BRN 
605308
Exposure limits
ACGIH: TWA 0.1 ppm; STEL 0.2 ppm (Skin)
Dielectric constant
7.0
Stability:
Stable. Flammable. Incompatible with strong oxidizing agents.
InChIKey
BHELZAPQIKSEDF-UHFFFAOYSA-N
LogP
1.79
CAS DataBase Reference
106-95-6(CAS DataBase Reference)
NIST Chemistry Reference
1-Propene, 3-bromo-(106-95-6)
EPA Substance Registry System
3-Bromopropene (106-95-6)
More
Less

Safety

Hazard Codes 
F,T,N
Risk Statements 
11-23/25-34-50-25-46-45
Safety Statements 
16-26-36/37/39-45-60-61-53
RIDADR 
UN 1099 3/PG 1
WGK Germany 
2
RTECS 
UC7090000
8-19
Autoignition Temperature
554 °F
TSCA 
Yes
HazardClass 
3
PackingGroup 
I
HS Code 
29033036
Hazardous Substances Data
106-95-6(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 120 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H314Causes severe skin burns and eye damage

H340May cause genetic defects

H350May cause cancer

H400Very toxic to aquatic life

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
337528
Product name
Allyl bromide
Purity
reagent grade, 97%, contains ≤1000 ppm propylene oxide as stabilizer
Packaging
250ml
Price
$58.2
Updated
2024/03/01
Sigma-Aldrich
Product number
8.01021
Product name
3-Bromo-1-propene
Purity
(stabilised) for synthesis
Packaging
1L
Price
$185
Updated
2024/03/01
Sigma-Aldrich
Product number
337528
Product name
Allyl bromide
Purity
reagent grade, 97%, contains ≤1000 ppm propylene oxide as stabilizer
Packaging
1l
Price
$179
Updated
2024/03/01
TCI Chemical
Product number
B0643
Product name
Allyl Bromide
Purity
>98.0%(GC)
Packaging
25g
Price
$23
Updated
2024/03/01
TCI Chemical
Product number
B0643
Product name
Allyl Bromide
Purity
>98.0%(GC)
Packaging
500g
Price
$92
Updated
2024/03/01
More
Less

Allyl bromide Chemical Properties,Usage,Production

Chemical Properties

Allyl bromide is a flammable liquid with an intense, acrid, persistent smell. It is insoluble in water but in alcohol, aether, acetone, carbon tetrachloride, and chloroform. Allyl bromide is used to synthesize other allyl compounds, to synthesize dyestuff and spice, and as a curative in the medicine industry. Allyl bromide has a very high mobility in soil. It is also used as a soil fumigant and as a contact poison. Allyl bromide induces unscheduled DNA synthesis in HeLa cells.

Uses

Allyl bromide is used as an alkylating agent in the synthesis of pharmaceuticals, polymers, adhesives, perfumes, biochemicals and other allylic compounds. It is used as precursor for the preparation of allyliczinc bromide by reacting it with zinc. It is also used in the preparation of allylethers like allyl decyl ether, allyl benzyl ether and allyl geranyl ether. It is also used in the preparation of R enantiomer of allyl phenyl carbinol (APC) such as 1-phenyl-3-butene, which is a valuable intermediate for drugs and agro-chemicals.

General Description

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.

Air & Water Reactions

Highly flammable. Slightly soluble in water.

Reactivity Profile

Allyl bromide decomposes upon heating and exposure to light, forming HBr (a strong reducing agent). Reacts violently with oxidizing agents. Can react exothermically with reducing agents to release hydrogen gas. In the presence of various catalysts (such as acids) or initiators, may undergo exothermic addition polymerization reactions.

Hazard

Strong irritant to skin and eyes, flammable, high fire risk. Upper respiratory tract irritant. Ques- tionable carcinogen.

Health Hazard

Exposures to allyl bromide cause severe eye and skin burns, irritation to the eyes, skin, and respiratory system. It is harmful when absorbed through the skin or inhaled in the workplace. Laboratory rats exposed for a prolonged period of time developed symptoms of poisoning, such as excessive salivation in a small number of animals, and severe gastric irritation. Vapors of allyl bromide may cause dizziness or suffocation, headache, coughing, and distressed breathing.

Safety Profile

Poison by ingestion and intraperitoneal routes. Mdly toxic by inhalation. Human mutation data reported. See also ALLYL CHLORIDE and ALLYL COMPOUNDS. Dangerous fire and explosion hazard when exposed to heat, flame, or oxidizers. When heated to decomposition it emits toxic fumes of Br-. To fight fire, use alcohol foam, water spray or mist, CO2, dry chemical

Synthesis

Allyl alcohol was synthesized from glycerol and formic acid under inert atmosphere, hydrolysed with NaOH and fractionally distilled to yield the 73% allyl alcohol water azeotrope. This was then reacted with 48% hydrobromic acid and sulfuric acid and the allyl bromide distilled as per the conventional method. It was then redistilled with 3A molecular sieves drying agent to yield the final product which is stored over additional 3A molecular sieves.

storage

Allyl bromide should be stored separate from oxidizing materials and alkalis in a cool, dry, well-ventilated location in tightly closed containers.

Shipping

UN1099 Allyl bromide, Hazard Class: 3; Labels: 3-Flammable liquid, 6.1-Poisonous materials

Purification Methods

Wash the bromide with NaHCO3 solution then distilled water, dry (CaCl2 or MgSO4), and fractionally distil. Protect it from strong light.

Incompatibilities

Vapor may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Heat or light exposure may cause decomposition and corrosive vapors.

Waste Disposal

In accordance with 40CFR 165 recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Precautions

Workers should wear positive pressure self-contained breathing apparatus (SCBA), goggles and a face shield, protective clothing for high concentrations of vapor, chemical protective clothing that is specifi cally recommended by the manufacturer to avoid poisoning. Workers should be careful as allyl bromide reacts with oxidizing materials and alkalis.

More
Less

Allyl bromide Suppliers

TCI Chemicals (India) Pvt. Ltd.
Tel
--
Fax
--
Email
sales-in@tcichemicals.com
Country
India
ProdList
6768
Advantage
58
Mody Chemi Pharma Ltd.
Tel
--
Fax
--
Email
modychem@gmail.com
Country
India
ProdList
30
Advantage
58
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
marketing@srlchem.com
Country
India
ProdList
4315
Advantage
58
Vardhaman P Golechha
Tel
--
Fax
--
Email
info@leonidchemicals.net
Country
India
ProdList
152
Advantage
58
Triveni chemicals
Tel
--
Fax
--
Email
sales@trivenichemical.com
Country
India
ProdList
6088
Advantage
58
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
India
ProdList
6905
Advantage
58
Amvee Chemicals
Tel
--
Fax
--
Country
India
ProdList
30
Advantage
58
ASM Organics
Tel
--
Fax
--
Country
India
ProdList
1185
Advantage
58
Clearsynth Labs
Tel
--
Fax
--
Email
fo@clearsynth.com
Country
India
ProdList
3887
Advantage
58
Precious Chemicals
Tel
--
Fax
--
Email
preciouschemicals@gmail.com
Country
India
ProdList
16
Advantage
58
Acid India
Tel
--
Fax
--
Country
India
ProdList
13
Advantage
58
Arham Enterprise
Tel
--
Fax
--
Country
India
ProdList
53
Advantage
58
Acid India Limited
Tel
--
Fax
--
Email
sales@acidindia.in
Country
India
ProdList
29
Advantage
58
Chemrich Fine Chemicals Pvt., Ltd.
Tel
--
Fax
--
Email
info@chemrichfine.com
Country
India
ProdList
399
Advantage
58
Modi Chemicals Industries
Tel
--
Fax
--
Country
India
ProdList
15
Advantage
58
Ramsun Rasayanics
Tel
--
Fax
--
Country
India
ProdList
35
Advantage
58
Loba Chemie Pvt., Ltd.
Tel
--
Fax
--
Email
@lobachemie.com
Country
India
ProdList
765
Advantage
58
Yogi Enterprise
Tel
--
Fax
--
Country
India
ProdList
22
Advantage
58
Neogen Chemicals Limited
Tel
--
Fax
--
Country
India
ProdList
151
Advantage
58
Ms Life Sciences
Tel
--
Fax
--
Country
India
ProdList
341
Advantage
58
Anand Agencies
Tel
--
Fax
--
Email
en@gmail.com
Country
India
ProdList
2332
Advantage
58
HiMedia Laboratories
Tel
--
Fax
--
Email
o@himedialabs.com
Country
India
ProdList
1841
Advantage
58
Pacific Organics Private Limited
Tel
--
Fax
--
Country
India
ProdList
8
Advantage
58
Tulip Chemicals Pvt., Ltd.
Tel
--
Fax
--
Email
hpk@tulipchemicals.com
Country
India
ProdList
28
Advantage
58
A. B. Enterprises
Tel
--
Fax
--
Country
India
ProdList
226
Advantage
58
Agrocel Industries Limited
Tel
--
Fax
--
Country
India
ProdList
16
Advantage
58
Oceanic Pharmachem Pvt. Ltd.
Tel
--
Fax
--
Email
info@oceanicpharmachem.com
Country
India
ProdList
2005
Advantage
58
Advent Chembio Pvt., Ltd.
Tel
--
Fax
--
Email
sales@adventchembio.com
Country
India
ProdList
623
Advantage
58
Dharani Export-Import Services (P) Ltd.
Tel
--
Fax
--
Email
info@dharani-exim.com
Country
India
ProdList
171
Advantage
58
Brisben Chemicals
Tel
--
Fax
--
Country
India
ProdList
508
Advantage
58
Shivam Pharma Chemicals
Tel
--
Fax
--
Email
info@shivampharma.com
Country
India
ProdList
656
Advantage
58
Sigma Chem International
Tel
--
Fax
--
Email
sigmachem9@gmail.com
Country
India
ProdList
43
Advantage
58
Loba Chemie Pvt Ltd
Tel
--
Fax
--
Country
India
ProdList
498
Advantage
58
Nova International
Tel
--
Fax
--
Country
India
ProdList
97
Advantage
58
Dhruv Chem Industries
Tel
--
Fax
--
Country
India
ProdList
36
Advantage
58
Rivashaa Agrotech Biopharma Pvt. Ltd.
Tel
--
Fax
--
Email
source@rivashaa.com
Country
India
ProdList
986
Advantage
58
Arene Life Sciences Limited
Tel
--
Fax
--
Country
India
ProdList
164
Advantage
58
Oxford laboratories
Tel
--
Fax
--
Country
India
ProdList
652
Advantage
58
Solaris Chemtech Industries Limited
Tel
--
Fax
--
Country
India
ProdList
9
Advantage
58
S. R. Chemical Specialities
Tel
--
Fax
--
Country
India
ProdList
90
Advantage
58
Faluck International
Tel
--
Fax
--
Country
India
ProdList
31
Advantage
58
Sontara Organo Industries
Tel
--
Fax
--
Country
India
ProdList
49
Advantage
58
Bhavika Chemicals Corporation
Tel
--
Fax
--
Country
India
ProdList
36
Advantage
58
Aniket Enterprises
Tel
--
Fax
--
Country
India
ProdList
27
Advantage
58
Azole Rasayanas India Private Limited
Tel
--
Fax
--
Email
info@azolerasayanas.com
Country
India
ProdList
681
Advantage
58
Avra Synthesis Pvt Ltd
Tel
--
Fax
--
Email
info@avrasynthesis.com
Country
India
ProdList
1603
Advantage
30
Mody Chemi-Pharma Limited
Tel
--
Fax
--
Country
India
ProdList
29
Advantage
58
Globe Chemie
Tel
--
Fax
--
Country
India
ProdList
101
Advantage
58
Ultima Chemicals
Tel
--
Fax
--
Country
India
ProdList
182
Advantage
58
Prabhat Chemi-Pharma Private Limited
Tel
--
Fax
--
Country
India
ProdList
22
Advantage
58
More
Less

View Lastest Price from Allyl bromide manufacturers

Hebei Miaoyin Technology Co.,Ltd
Product
Allyl bromide 106-95-6
Price
US $20.00/kg
Min. Order
1kg
Purity
99.99%
Supply Ability
10000
Release date
2023-04-18
Hebei Yanxi Chemical Co., Ltd.
Product
3-bromopropene 106-95-6
Price
US $0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
20tons
Release date
2023-10-13
Hebei Chuanghai Biotechnology Co,.LTD
Product
3-bromopropene 106-95-6
Price
US $19.00/KG
Min. Order
1KG
Purity
99.%
Supply Ability
10 ton
Release date
2024-08-15

106-95-6, Allyl bromideRelated Search:


  • BROMALLYLENE
  • 2-PROPENYL BROMIDE
  • ALLYL BROMIDE
  • 3-BROMOPROPYLENE
  • 3-BROMOPROPENE
  • 3-BROMO-1-PROPENE
  • CH2=CHCH2Br
  • Propene, 3-bromo-
  • Propene,3-bromo-
  • ALLYL BROMIDE, REAGENTPLUS, 99%
  • ALLYL BROMIDE STAB. WITH SILVER
  • Allyl bromide, stabilized, 99%
  • 3-BROMOPROPENE,REAGENT
  • 3-Bromo-1-propene (stabilised) for synthesis
  • Allyl bromide, Stabilized with 300 to 1000ppm Propylene oxide
  • 1-Bromo-2-propene
  • 1-Propene,3-bromo-
  • 3-bromo-1-propen
  • 3-bromopropane
  • ALLYL BROMIDE, 98%ALLYL BROMIDE, 98%ALLYL BROMIDE, 98%ALLYL BROMIDE, 98%
  • Аллил бромистый, 2-пропенилбромид, 3-бромпропен, Allyl bromide, 3-Bromo-1-propene
  • 3-bromo-prop-1-ene
  • 3-bromo-propen
  • 3-Brompropen
  • Allylbromid
  • allylbromide(3-bromopropene)
  • bromo-3propene
  • Bromoallylene
  • ALLYL BROMIDE pure
  • Allyl broMide, stabilized, 99% 250ML
  • (DG) Allyl bromide 2g [106-95-6]
  • Allyl bromide, 99%, stab. with 300-1000ppm Propylene oxide
  • 3-Bromoprop-1-ene 99%
  • ALLYLBROMID-R
  • Allyl bromide, 98+%
  • Allyl bromide, 99%, stabilized
  • 3-Bromo-1-propene 3-Bromopropylene
  • 3-BROMO-1-PROPENE (STABILISED) FOR SYNTH
  • 3-BroMopropene/ Allyl broMide
  • Allyl Bromide (Stabilized with Propylene Oxide)
  • 3-BroMopropene, Stabilized with ca. 300 ppM Propylene Oxide, Reagent
  • Allyl broMide reagent grade, 97%, contains <=1000 ppM propylene oxide as stabilizer
  • Allyl broMide ReagentPlus(R), 99%, contains <=1000 ppM propylene oxide as stabilizer
  • 3 - allyl broMide
  • Allyl Bromide &gt
  • Allyl bromide,99%
  • Allyl bromide ISO 9001:2015 REACH
  • Allyl bromideF
  • Allyl bromide, GR 99%+
  • ALLYL BROMIDE For Synthesis
  • Eugenol Impurity 18
  • Eugenol Impurity 1
  • 3-Bromo-1-Propylene
  • Allyl Bromide 98% For Synthesis
  • Biapenem Impurity 20
  • 106-95-6
  • 106-95-9
  • 203-446-6