MedKoo Cat#: 130332 | Name: 8-Bromo-1-octanol
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

8-Bromo-1-octanol is vital for esterification and was used in the synthesis of (Z)-14-methyl-9-pentadecenoic acid and various other molecules.

Chemical Structure

8-Bromo-1-octanol
8-Bromo-1-octanol
CAS# 50816-19-8

Theoretical Analysis

MedKoo Cat#: 130332

Name: 8-Bromo-1-octanol

CAS#: 50816-19-8

Chemical Formula: C8H17BrO

Exact Mass: 208.0463

Molecular Weight: 209.13

Elemental Analysis: C, 45.95; H, 8.19; Br, 38.21; O, 7.65

Price and Availability

Size Price Availability Quantity
5g USD 250.00 2 Weeks
25g USD 450.00 2 Weeks
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Related CAS #
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Synonym
8-Bromo-1-octanol; Octamethylene bromohydrin; 8-Bromooctan-1-ol
IUPAC/Chemical Name
8-bromooctan-1-ol
InChi Key
GMXIEASXPUEOTG-UHFFFAOYSA-N
InChi Code
InChI=1S/C8H17BrO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2
SMILES Code
BrCCCCCCCCO
Appearance
Liquid
Purity
>96% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 209.13 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Gupta N, Shallu, Kad GL, Singh J. First total synthesis of acetylenic alcohol 15-methyltricosa-2,4-diyne-1, 6-diol (strongylodiol-G) derived from marine sponge. Nat Prod Res. 2014;28(7):424-30. doi: 10.1080/14786419.2013.867855. Epub 2014 Jan 15. PMID: 24423029. 2. Saga Y, Hayashi K, Mizoguchi T, Tamiaki H. Biosynthesis of bacteriochlorophyll c derivatives possessing chlorine and bromine atoms at the terminus of esterifying chains in the green sulfur bacterium Chlorobaculum tepidum. J Biosci Bioeng. 2014 Jul;118(1):82-7. doi: 10.1016/j.jbiosc.2013.12.023. Epub 2014 Feb 1. PMID: 24495924. 3. Carballeira NM, Sanabria D, Oyola D. An improved synthesis for the (Z)-14-methyl-9-pentadecenoic acid and its topoisomerase I inhibitory activity. ARKIVOC. 2007;2007(viii):49-57. PMID: 17680032; PMCID: PMC1939943. 4. Chiron R. New synthesis of royal jelly acid. J Chem Ecol. 1982 Apr;8(4):709-13. doi: 10.1007/BF00988312. PMID: 24415118.