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Sigma-Aldrich

6-Bromohexanoyl chloride

97%

Synonym(s):

6-Bromocaproyl chloride, 6-Bromohexanoic acid chloride

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About This Item

Linear Formula:
Br(CH2)5COCl
CAS Number:
22809-37-6
Molecular Weight:
213.50
Beilstein:
1749739
EC Number:
245-236-7
MDL number:
MFCD00000761
UNSPSC Code:
12352100
PubChem Substance ID:
24854112
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.486 (lit.)

bp

130 °C/20 mmHg (lit.)

density

1.395 g/mL at 25 °C (lit.)

functional group

acyl chloride
bromo

SMILES string

ClC(=O)CCCCCBr

InChI

1S/C6H10BrClO/c7-5-3-1-2-4-6(8)9/h1-5H2

InChI key

HBPVGJGBRWIVSX-UHFFFAOYSA-N

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Application

6-Bromohexanoyl chloride has been used in preparation of:
  • (S)- or (R)-N-(6-bromohexanoyl)-α-methylbenzylamine
  • 1-bromoheptadecan-6-one and 1-bromooctadecan-6-one

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H335

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

EUH014

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV2820
MKCN9986
MKCK5274
MKBZ3141V
MKBT7315V

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An enantiomeric discrimination in aqueous mixed chiral micelles through hydrogen bonding.
Jursic BS.
Tetrahedron Letters, 34(6), 963-966 (1993)
Tae Yang Son et al.
Polymers, 12(11) (2020-11-27)
In this study, novel crosslinked pore-filling membranes were fabricated by using a centrifugal force from the cylindrical centrifugal machine. For preparing these crosslinked pore-filling membranes, the poly(phenylene oxide) containing long side chains to improve the water management (hydrophilic), porous polyethylene
Tomás Holas et al.
Bioorganic & medicinal chemistry, 14(9), 2896-2903 (2005-12-27)
Transkarbam 12 (5-(dodecyloxycarbonyl)pentylammonium-5-(dodecyloxycarbonyl)pentylcarbamate, T12) is a highly active transdermal permeation enhancer. In this study, ketone, amide, and alkane analogs of T12 have been synthesized and evaluated for their permeation-enhancing activity using porcine skin and theophylline as a model drug. Replacement
Ji Eon Chae et al.
Polymers, 13(5) (2021-03-07)
Polystyrene-based polymers with variable molecular weights are prepared by radical polymerization of styrene. Polystyrene is grafted with bromo-alkyl chains of different lengths through Friedel-Crafts acylation and quaternized to afford a series of hydroxide-ion-conducting ionomers for the catalyst binder for the

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