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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.)

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

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’.

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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
An enantiomeric discrimination in aqueous mixed chiral micelles through hydrogen bonding.
Jursic BS.
Tetrahedron Letters, 34(6), 963-966 (1993)
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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