Hydrobromic acid (33% in acetic acid)
Hydrobromic acid (33% in acetic acid)

Hydrobromic acid (33% in acetic acid)

MOQ : 1 Kilograms

Hydrobromic acid (33% in acetic acid) Specification

  • Boiling point
  • Varies due to mixture; HBr 122C, AcOH 118C
  • HS Code
  • 28111990
  • Structural Formula
  • HBr (Hydrobromic Acid) in CH3COOH (Acetic Acid)
  • Taste
  • Sharp, sour, acidic
  • Molecular Formula
  • HBr in CH3COOH
  • Refractive Rate
  • ~1.39 at 20C
  • Smell
  • Pungent, acetic
  • Molecular Weight
  • Approx. 94.45 (HBr); 60.05 (Acetic Acid)
  • Classification
  • Inorganic Acid
  • Organic Acid Types
  • Acetic Acid
  • Inorganic Acid Types
  • Hydrobromic Acid
  • Grade
  • Laboratory/Reagent Grade
  • Purity
  • 33% w/w in Acetic Acid
  • Application
  • Pharmaceuticals, Laboratory Reagent, Chemical Synthesis
  • Appearance
  • Clear colorless to pale yellow solution
  • CAS No
  • 10035-10-6 (HBr), 64-19-7 (Acetic Acid)
  • EINECS No
  • 233-113-0 (HBr), 200-580-7 (Acetic Acid)
  • Other Names
  • Hydrobromic Acid in Acetic Acid; HBr/AcOH solution
  • Usage
  • Used as a brominating agent in organic reactions; pharmaceutical intermediate
  • Melting Point
  • Not applicable (liquid mixture)
  • Density
  • 1.4 Gram per cubic centimeter(g/cm3)
  • Solubility
  • Soluble in water and ethanol
  • Raw Material
  • Hydrobromic Acid, Acetic Acid
  • Production Method
  • Prepared by reaction of HBr gas with acetic acid under controlled conditions
  • Packaging
  • HDPE drums, glass bottles, custom packaging on request
  • Stability
  • Stable under recommended storage conditions
  • Transport Information
  • UN 1788, Class 8, Packing Group II
  • Vapour Pressure
  • Not determined for mixture
  • pH
  • <1 (strongly acidic)
  • Handling Precautions
  • Wear protective gloves, clothing, eye/face protection
  • Hazards
  • Corrosive, causes severe skin burns and eye damage
  • Water Content
  • Low, due to acetic acid solvent
  • Storage Conditions
  • Keep container tightly closed, store in cool, dry, well-ventilated place
  • Shelf Life
  • 12 months in sealed container
 

Hydrobromic acid (33% in acetic acid) Trade Information

  • Minimum Order Quantity
  • 1 Kilograms
  • Supply Ability
  • 100 Kilograms Per Month
  • Delivery Time
  • 7 Days
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
 

About Hydrobromic acid (33% in acetic acid)

Name of Product Hydrobromic acid (33% in acetic acid) IUPAC Name bromane
CAS No 10035-10-6 InChI InChI=1S/BrH/h1H
Formula HBr InChI Key CPELXLSAUQHCOX-UHFFFAOYSA-N
Other name / synonyms Hydrogen bromide Canonical SMILES Br

HYDROBROMIC ACID CAS 10035-10-6

10035-10-6 EC Number 233-113-0

bromane from ILO-ICSC 233-113-0

Bromowodor ICSC Number 282

Bromwasserstoff RTECS Number MW3850000

Broomwaterstof UN Number 1048 (anhydrous)

Acido bromidrico
1788

Anhydrous hydrobromic acid UNII 3IY7CNP8XJ

Acide bromhydrique Wikipedia Hydrobromic acid

Bromowodor [Polish]
Hydrogen bromide

(3h)hydrogen bromide


Broomwaterstof [Dutch] Assay Not less than 33 %

(82br)hydrogen bromide Description Clear, colourless to pale yellow , fuming liquid

Hydrogen bromide (HBr) Water Not more than 1.0 %

Bromwasserstoff [German]


UNII-3IY7CNP8XJ


Acido bromidrico [Italian]


Hydrogen bromide, anhydrous


Acide bromhydrique [French]


Acido bromhidrico [Spanish]


Hydrobromic Acid, anyhydrous


HSDB 570


CHEBI:47266


CPELXLSAUQHCOX-UHFFFAOYSA-N


EINECS 233-113-0


Bromure d'hydrogene anhydre [French]


UN1048


UN1788


Bromuro de hidrogeno anhidro [Spanish]


Hydrobromic acid solution


Hydrogen bromide solution


Hydrobromic acid 62% by weight or more HBr


HBR


Hydrogen bromide in acetic acid


bromum


hydrobrornide


hydrogenbromide


hydro bromide


hyrobromic acid


hydrogen-bromide


hydrobrornic acid


Acido bromhidrico


hydro-bromic acid


bromure d'hydrogene


Hydrogen monobromide


BROMO GROUP


Hydrobromic acid 48%


Hydrobromic acid,48%


ACMC-1BUCJ


3IY7CNP8XJ


Hydrobromic acid solution


35Br


Bromure d'hydrogene anhydre


hydrogen bromide 33% w/w


AC1L18UA


Bromuro de hidrogeno anhidro


Hydrogen bromide, anhydrous-


KSC174Q6R


295418_ALDRICH


35002_RIEDEL


CHEMBL1231461


18710_FLUKA


18720_FLUKA


18735_FLUKA


23828_FLUKA


35002_FLUKA


CHEBI:22927


CTK0H4868


MolPort-001-760-361


WKBOTKDWSSQWDR-UHFFFAOYSA-N


18710_SIAL


18720_SIAL


18735_SIAL


KST-1A1208


KST-1A1544


LTBB002754


Hydrogen Bromide - Ethanol Reagent


244260_SIAL


248630_SIAL


268003_SIAL


337978_SIAL


339245_SIAL


438065_SIAL


Hydrogen Bromide - Methanol Reagent


AR-1A4200


AR-1A7207


AKOS015833690


EBD2198018


MCULE-6124492894


RP18384


RTR-024697


UN 1048


UN 1788


Hydrogen bromide 33% in ACETIC ACID


BP-21021


LS-77039


AB1010073


RT-000115


RT-000168


TL8000044


11071-85-5 (hydrogen bromide (HBr2))


FT-0623202


FT-0627106


C13645


HYDROBROMIC ACID, ACS 49% UN1788(II)


A800104


Hydrogen bromide, anhydrous [UN1048] [Poison gas]


Hydrobromic acid, with more than 49% hydrobromic acid


Hydrogen bromide, anhydrous [UN1048] [Poison gas]


Hydrobromic acid, with not more than 49% hydrobromic acid


Hydrobromic acid, with more than 49% hydrobromic acid [UN1788] [Corrosive]


Hydrobromic acid, with more than 49% hydrobromic acid [UN1788] [Corrosive]


Hydrobromic acid, with not more than 49% hydrobromic acid [UN1788] [Corrosive]


Hydrobromic acid, with not more than 49% hydrobromic acid [UN1788] [Corrosive]


62140-56-1


BRO



Applications in Chemical Synthesis

Hydrobromic acid (33% in acetic acid) serves as an effective brominating agent in organic and pharmaceutical synthesis. Its distinct composition enhances reactivity for targeted chemical processes, making it an essential laboratory and industrial reagent. Aside from synthesis, it is employed as an intermediate in pharmaceutical manufacturing and complex organic transformations, benefiting from its high purity and controlled acidity.


Safe Handling and Storage

This mixture is intensely acidic and highly corrosive, necessitating strict safety measures during handling. It should be managed while wearing appropriate protective gloves, clothing, and eye/face protection. For safety and longevity, keep the container tightly closed in a cool, dry, and well-ventilated area. Adherence to these guidelines preserves stability and extends the solution's shelf life to 12 months in sealed conditions.

FAQ's of Hydrobromic acid (33% in acetic acid):


Q: How is hydrobromic acid (33% in acetic acid) produced?

A: This solution is prepared by reacting hydrobromic acid gas (HBr) with acetic acid (CH3COOH) under carefully controlled conditions, ensuring high purity and accurate concentration for laboratory and synthesis use.

Q: What are the primary uses of hydrobromic acid in acetic acid solutions?

A: It is widely used as a brominating agent in organic chemistries, pharmaceutical manufacturing, and laboratory research. Its composition is tailored for precision in chemical reactions and intermediate compound production.

Q: When should I replace or dispose of this product?

A: Hydrobromic acid (33% in acetic acid) has a shelf life of 12 months when stored securely in sealed containers. Replace or safely dispose of the solution once this period lapses or if container integrity is compromised.

Q: Where should this product be stored for optimal stability?

A: Store in a cool, dry, and well-ventilated space, within tightly sealed HDPE drums or glass bottles. Avoid exposure to moisture or temperature extremes to maintain stability and safety.

Q: What safety measures should be taken while handling this acid mixture?

A: Always wear chemical-resistant gloves, protective clothing, and suitable eye/face protection when handling. Avoid exposure to skin, eyes, and inhalation to prevent severe burns and health hazards.

Q: What is the benefit of using hydrobromic acid in acetic acid rather than aqueous solutions?

A: Using acetic acid as the solvent ensures lower water content, which can be advantageous for moisture-sensitive reactions and for achieving higher selectivity and yield in organic synthesis.

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