Skip to Content
Merck
All Photos(1)

Documents

448729

Sigma-Aldrich

9-Bromo-1-nonanol

95%

Synonym(s):

Nonamethylene bromohydrin

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
Br(CH2)9OH
CAS Number:
55362-80-6
Molecular Weight:
223.15
Beilstein:
1737525
MDL number:
MFCD00063348
UNSPSC Code:
12352100
PubChem Substance ID:
24868427
NACRES:
NA.22

Assay

95%

bp

125-126 °C/2 mmHg (lit.)

mp

33-35 °C (lit.)

SMILES string

OCCCCCCCCCBr

InChI

1S/C9H19BrO/c10-8-6-4-2-1-3-5-7-9-11/h11H,1-9H2

InChI key

USJDOLXCPFASNV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis of the diacetylenic phospholipids 1, 2-(10', 12'-heptadecadiynoyl)-sn-glycero-3-phophatidylcholine and 1, 2-(4', 6'-tricosadiynoyl)-sn-glycero-3-phophatidylcholine.
Hennies PT, et al.
Journal of the Brazilian Chemical Society, 12(1), 64-72 (2001)
In vitro enzymatic oxidation of a fluorine-tagged sulfido substrate analogue: a 19F NMR investigation.
Tremblay AE, et al.
Magnetic Resonance in Chemistry, 44(6), 629-632 (2006)
Néstor M Carballeira et al.
Chemistry and physics of lipids, 145(1), 37-44 (2006-11-28)
The first total syntheses for the (Z)-15-methyl-10-hexadecenoic acid and the (Z)-13-methyl-8-tetradecenoic acid were accomplished in seven steps and in 31-32% overall yields. The (trimethylsilyl)acetylene was the key reagent in both syntheses. It is proposed that the best synthetic strategy towards
Sequential alkynylation of ω-bromoalkyl triflates: facile access to unsymmetrical non-conjugated diynes including precursors to diene.
Armstrong-Chong RJ, et al.
Tetrahedron, 60(45), 10239-10244 (2004)
Highly ion conductive flexible films composed of network polymers based on polymerizable ionic liquids.
Washiro S, et al.
Polymer, 45(5), 1577-1582 (2004)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service