Basic information
- CAS
2067-33-6- Standard SMILES
O=C(O)CCCCBr- InChIKey
WNXNUPJZWYOKMW-UHFFFAOYSA-N- Molecular formula
- C5H9BrO2
- Average molar mass
- 181.03 g/mol
- Monoisotopic mass
- 179.97859163
Names & identifiers
- Preferred name
- 5-Bromovaleric acid
- IUPAC
- 5-bromopentanoic acid
- English name
- 5-Bromovaleric acid
- Molecular formula
- C5H9BrO2
- Molecular weight
- 181.03
Names & synonyms
Show more names
Database identifiers
- CAS
2067-33-6- PubChem CID
- 16368
- DTXSID
DTXSID2062163- UNII
- Z7DY4J7HZR
- EC Number
- 218-185-3
- Nikkaji
- J22.500B
Properties
Computed structural properties
- XLogP
- 1.4
- Topological polar surface area
- 37.3 Ų
- Hydrogen bond donors
- 1
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 4
- Heavy atoms
- 8
- Formal charge
- 0
- Complexity
- 72.8
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 38 · 38-40 °C (lit.)
- Boiling point
- 142 · 142-145 °C (13 mmHg)
- Density
- 1.421 · 1.4210 (rough estimate)
- refractive index
- 1.479 · 1.4790 (estimate)
- Flash point
- 230 °F · >230 °F
- storage temp.
- 30 °C · Store below +30°C.
- solubility
- 95 % · 95% ethanol: soluble50mg/mL, clear, colorless to faintly yellow
- form
- Crystals or Crystalline Powder
- pka
- 4 · 4+-.0.10(Predicted)
- color
- Yellow to light brown
- Water Solubility
- Soluble in ethanol. Insoluble in water.
- BRN
- 1745664 · 1745664
- InChI
- 1S/C5H9BrO2/c6-4-2-1-3-5(7)8/h1-4H2,(H,7,8)
- InChIKey
- WNXNUPJZWYOKMW-UHFFFAOYSA-N
- SMILES
- OC(=O)CCCCBr
- CAS DataBase Reference
- 2067 · 2067-33-6(CAS DataBase Reference)
- FDA UNII
- 7 DY4J7HZR · Z7DY4J7HZR
- NIST Chemistry Reference
- 5 · Valeric acid, 5-bromo(2067-33-6)
- EPA Substance Registry System
- 5 · 5-Bromovaleric acid (2067-33-6)
- UNSPSC Code
- 12352106 · 12352106
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319-H335
- Precautionary statements
- 261 · P261-P264-P271-P280-P302+P352-P305+P351+P338
- target organs
- Respiratory system
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xi
- Risk Statements
- 36 · 36/37/38
- Safety Statements
- 26 · 26-36
- RIDADR
- 3261 · UN3261
- WGK Germany
- 3 · 3
- TSCA
- TSCA listed
- HazardClass
- 8 · 8
- PackingGroup
- III
- HS Code
- 29159080 · 29159080
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 2 Skin · Eye Irrit. 2Skin Irrit. 2STOT SE 3
- REACH Registrations
- Active
Safety & regulation
GHS classification
GHS Classification
Danger
H302 (15.3%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P319, P321, P330, P332+P317, P337+P317, P362+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 59 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Regulatory Information
Status: Active Update: 09-04-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/19312
5-Bromovaleric acid: Does not have an individual approval but may be used under an appropriate group standard
Toxicology
Safety data
- PPE
- dust mask type N95 (US), Eyeshields, Gloves
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN3261
- hs_code
- 29159080
- risk_code
- 36/37/38
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 26-36
- hazard_class
- 8
- Storage Class
- 11 - Combustible Solids
- packing_group
- III
- target organs
- Respiratory system
- Hazard statements
- H315-H319-H335
- REACH Registrations
- Active
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
- Precautionary statements
- P261-P264-P271-P280-P302+P352-P305+P351+P338
Chemistry & industry
Uses & manufacturing
Applications
Description5-Bromovaleric acid is an important raw material for organic synthesis and a commonly used reagent for chemical reactions. It can be used in the synthesis of the natural mosquito egg-laying pheromone red-6-acetoxy-5-hexadecanolactone, alkylammonium amphoteric amino acid derivatives and water-soluble nanoplatelets.
Uses5-Bromovaleric acid is used in the synthesis of inhibitors for aminoglycoside resistant bacteria. 5-Bromovaleric acid is also used in the preparation of sequence specific base pair mimics as topoisomerase IB inhibitors.
Preparation methods
PreparationIn a 250 mL three-necked flask equipped with a stirrer and thermometer, a dichloromethane solution of 5-bromopentanol and the crown ether catalyst were added. The stirrer was started, and finely ground potassium permanganate was added in small batches while stirring rapidly, which took about 1 hour. After the addition was complete, stirring continued until the reaction temperature no longer rose. The reaction time was then determined using a TLC plate (different polarities diffuse at different rates on the plate). Using n-butanol:acetic acid:water = 4:1:1 as the developing solvent, the plate was spotted every 0.5 hours, ultimately determining that the reaction was complete after 1 hour. During the reaction, a large amount of manganese dioxide precipitate was produced. The reaction mixture was filtered, washed with water to remove the aqueous phase, and then washed with NaOH solution to remove the crown ether and CH2Cl2. The sodium 5-bromopentanate in the aqueous phase was then washed with acid, and the bottom layer was taken out to obtain the initial product. After drying, 16.2 g of 5-Bromovaleric acid was obtained, with a yield of 90%.
Upstream & downstream products
Downstream products
Suppliers100 total
Related reactions
Compound notes
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