Skip to Content
Merck
CN
All Photos(2)

Documents

Safety Information

292389

Sigma-Aldrich

2-Bromoheptane

technical grade

Sign Into View Organizational & Contract Pricing
All Photos(2)
Synonym(s):
1-Methylhexyl bromide
Linear Formula:
CH3CH2CH2CH2CH2CHBrCH3
CAS Number:
1974-04-5
Molecular Weight:
179.10
Beilstein:
1731556
EC Number:
217-824-3
MDL number:
MFCD00000164
UNSPSC Code:
12352100
PubChem Substance ID:
24857582
NACRES:
NA.22

grade

technical grade

Quality Level

100

refractive index

n20/D 1.447 (lit.)

bp

64-66 °C/21 mmHg (lit.)

density

1.142 g/mL at 25 °C (lit.)

SMILES string

CCCCCC(C)Br

InChI

1S/C7H15Br/c1-3-4-5-6-7(2)8/h7H,3-6H2,1-2H3

InChI key

HLAUCEOFCOXKNF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2-Bromoheptane has been used in the preparation of:
  • racemic alcohol, 2-methylheptanol
  • glutathione (GSH) derivatives
  • GSH analog that contains tetrazole isostere (Tet-sHep)

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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

J Boruwa et al.
Bioorganic & medicinal chemistry letters, 14(13), 3571-3574 (2004-06-05)
The absolute stereochemistry of the new antifungal and antibacterial antibiotic produced by Streptomyces sp.201 has been established by achieving the total synthesis of the product. A series of analogues have also been synthesized by changing the side chain and their
Danny Burg et al.
Bioorganic & medicinal chemistry letters, 12(12), 1579-1582 (2002-06-01)
Glutathione (GSH) conjugates inhibit enzymes that are involved in drug metabolism and drug resistance, but their cellular uptake is very low. To improve membrane-permeability, we synthesized a novel GSH-conjugate analogue with a tetrazole carboxylate isostere at the glycine position. Introduction

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