5-Bromovaleric acid

HCID 16368

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

5-Bromovaleric acid5-BROMOPENTANOIC ACID2067-33-6Pentanoic acid, 5-bromo-5-Bromo-n-valeric acidValeric acid, 5-bromo-MFCD000044145-bromo valeric acid5-bromoval eric acidValeric acid, 5-bromoEINECS 218-185-3UNII-Z7DY4J7HZR
Show more names
eric acid5-valeric5-BromovaL5-BROMOVALENC ACID5-bromoacetic acidRARECHEM AL BO 01815-BROMRVALERIC ACID5-bromo-pentanoicaci
.delta.-Bromovaleric acidZ7DY4J7HZR5-BROMOPENTANOICACIDSCHEMBL214058DTXSID2062163NSC-53507AKOS000120301PD192647

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

Experimental & physicochemical properties

Chemical ClassesOther Classes -> Organic Acids
SpringerMaterials PropertiesNuclear quadrupole resonance spectroscopy
Vapor Pressure0.01 [mmHg]
Physical DescriptionWhite crystalline powder; [Alfa Aesar MSDS]

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.

Safety & regulation

GHS classification

GHS Classification · 4 items

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 · 2 items

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

Hazards SummaryCauses burns; Inhalation may cause corrosive injuries to upper respiratory tract and lungs; [Alfa Aesar MSDS] See 3-Bromopropionic acid.
Hazard Classes and CategoriesAcute Tox. 4 (15.3%)

Toxicology

Adverse EffectsDermatotoxin - Skin burns.

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

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationPentanoic acid, 5-bromo-: ACTIVE
Applications · 2 items

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 · 1 item

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

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖北瑞泰医药科技有限公司15335880183
INTATRADE GmbH+49 3493/605464 · [email protected]

Related reactions

60 records

Compound notes

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