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448729

Sigma-Aldrich

9-Bromo-1-nonanol

95%

Synonym(s):

Nonamethylene bromohydrin

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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

Quality Level

100

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

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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)

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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)
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