ChemicalBook >> CAS DataBase List >>8-Bromo-1-octanol

8-Bromo-1-octanol

CAS No.
50816-19-8
Chemical Name:
8-Bromo-1-octanol
Synonyms
8-bromooctan-1-ol;S,1000;8-BROMOOCTANOL;8-bromo-1-octano;8-Bromo-1-actanol;8-BROMO-1-OCTANOL;8-BroMo-1-oCLanol;8-Bromooctane-1-ol;1-bromo-octan-8-ol;1-Octanol, 8-bromo-
CBNumber:
CB6271684
Molecular Formula:
C8H17BrO
Molecular Weight:
209.12
MDL Number:
MFCD00010388
MOL File:
50816-19-8.mol
MSDS File:
SDS
Last updated:2026-05-28 05:41:18
Product description Number Pack Size Price
8-Bromo-1-octanol 95% 294144 1g $60.6
8-Bromo-1-octanol 95% 294144 5g $201
8-Bromo-1-octanol >90.0%(GC) B1729 5g $126
8-Bromo-1-octanol >90.0%(GC) B1729 25g $402
8-Bromooctan-1-ol TRC-B997403-500MG 500mg $78
More product size

8-Bromo-1-octanol Properties

Boiling point 79-80 °C/0.07 mmHg (lit.)
Density 1.22 g/mL at 25 °C (lit.)
refractive index n20/D 1.480(lit.)
Flash point >230 °F
storage temp. 2-8°C
solubility Chloroform (Sparingly), Ethyl Acetate (Slightly)
form Oil
pka 15.19±0.10(Predicted)
color Colourless
Specific Gravity 1.22
BRN 1900837
InChI InChI=1S/C8H17BrO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2
InChIKey GMXIEASXPUEOTG-UHFFFAOYSA-N
SMILES C(O)CCCCCCCBr
CAS DataBase Reference 50816-19-8(CAS DataBase Reference)
NIST Chemistry Reference 8-Bromo-1-octanol(50816-19-8)
EPA Substance Registry System 1-Octanol, 8-bromo- (50816-19-8)
UNSPSC Code 12352200
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280a-P305+P351+P338-P321-P332+P313-P337+P313
PPE Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Risk Statements  36-38
Safety Statements  23-24/25-37-26
WGK Germany  3
TSCA  TSCA listed
HS Code  29055900
Storage Class 10 - Combustible liquids
NFPA 704
1
2 0

8-Bromo-1-octanol price More Price(65)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 294144 8-Bromo-1-octanol 95% 50816-19-8 1g $60.6 2026-04-30 Buy
Sigma-Aldrich 294144 8-Bromo-1-octanol 95% 50816-19-8 5g $201 2026-04-30 Buy
TCI Chemical B1729 8-Bromo-1-octanol >90.0%(GC) 50816-19-8 5g $126 2026-04-30 Buy
TCI Chemical B1729 8-Bromo-1-octanol >90.0%(GC) 50816-19-8 25g $402 2026-04-30 Buy
TRC TRC-B997403-500MG 8-Bromooctan-1-ol 50816-19-8 500mg $78 2026-06-03 Buy
Product number Packaging Price Buy
294144 1g $60.6 Buy
294144 5g $201 Buy
B1729 5g $126 Buy
B1729 25g $402 Buy
TRC-B997403-500MG 500mg $78 Buy

8-Bromo-1-octanol Chemical Properties,Uses,Production

Chemical Properties

Clear colorless to yellow liquid

Uses

It is used to produce 8-phenylselanyl-octan-1-ol by reaction with diphenyl-diselane. The reaction occurs with reagent sodium borohydride and solvent ethanol at ambient temperature. The yield is about 96%. 8-Bromo-1-octanol was used in the synthesis of (E)-10-hydroxy-2-decenoic acid (royal jelly acid)1. It was also used in the synthesis of (Z)-14-methyl-9-pentadecenoic acid.

reaction suitability

reagent type: cross-linking reagent

Synthesis

1,8-Octanediol

629-41-4

8-Bromo-1-octanol

50816-19-8

The general procedure for the synthesis of 8-bromo-1-octanol from 1,8-octanediol was as follows: 16 g (110 mmol) of 1,8-octanediol was dissolved in 250 ml of toluene. To the solution was added 15.5 ml of hydrobromic acid (137 mmol, 1.25 eq., 48% aqueous solution), after which the reaction mixture was connected to a Dean-Stark manifold and refluxed to remove the water produced by the reaction. After 8 hours of reaction, the mixture was cooled to room temperature and washed sequentially twice with distilled water and once with brine. After drying over anhydrous sodium sulfate, the mixture was filtered and the solvent evaporated to give 8-bromo-1-octanol in quantitative yield. Nuclear magnetic resonance hydrogen spectroscopy (NMR) showed trace residues of toluene which did not affect the subsequent reaction. Densitometry (D2O calibration): 1.23 g/ml (literature value: 1.22 g/ml).13C NMR (CDCl3, ppm) data were as follows: 62.95 (CH2OH), 34.04 (BrCH2CH2), 32.78/32.71 (BrCH2 and CH2CH2OH), 29.23/28.73/ 28.09/25.65 (CH2).

References

[1] Patent: WO2018/108948, 2018, A1. Location in patent: Page/Page column 55
[2] Tetrahedron, 2008, vol. 64, # 30-31, p. 7369 - 7377
[3] Journal of the American Chemical Society, 1992, vol. 114, # 13, p. 5281 - 5294
[4] Phytochemistry, 1996, vol. 42, # 6, p. 1617 - 1620
[5] Tetrahedron Letters, 2002, vol. 43, # 15, p. 2745 - 2747

629-41-4
50816-19-8
Synthesis of 8-Bromo-1-octanol from 1,8-Octanediol
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View Lastest Price from 8-Bromo-1-octanol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
8-Bromo-1-octanol pictures 2025-04-04 8-Bromo-1-octanol
50816-19-8
1KG 98% 1ton Henan Aochuang Chemical Co.,Ltd.
8-Bromo-1-octanol pictures 2019-07-06 8-Bromo-1-octanol
50816-19-8
$1.00 1kg 96%+ Career Henan Chemical Co
1-Octanol, 8-bromo- 8-bromo-1-octano 1-bromo-octan-8-ol 8-BROMOOCTANOL 8-BROMO-1-OCTANOL 8-Bromo-1-actanol S,1000 OCTAMETHYLENE BROMOHYDRIN 8-Bromooctane-1-ol 8-Hydroxyoctyl bromide 8-BROMO-1-OCTANOL 90+% 8-BroMo-1-oCLanol 8-Bromo-1-octanol > Fulvestrant Impurity 71 8-bromooctan-1-ol 50816-19-8 BrCH28OH C8H17BrO Oxygen Compounds Organic Building Blocks C7 to C8 Alcohols Building Blocks 蠅-Functional Alkanols, Carboxylic Acids, Amines & Halides 蠅-Bromoalkanols Alcohols Bifunctional Crosslinkers Building Blocks C7 to C8 Chemical Biology Chemical Synthesis Linkers Organic Building Blocks Oxygen Compounds Peptide Chemistry OLED materials,pharm chemical,electronic omega-Bromoalkanols omega-Functional Alkanols, Carboxylic Acids, Amines & Halides Linear hydrocarbon series