Skip to Content
Merck
All Photos(1)

Documents

Safety Information

530409

Sigma-Aldrich

Propargyl bromide solution

80 wt. % in xylene

Synonym(s):

3-Bromo-1-propyne

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

About This Item

Linear Formula:
HC≡CCH2Br
CAS Number:
106-96-7
Molecular Weight:
118.96
Beilstein:
605309
MDL number:
MFCD00000241
UNSPSC Code:
12352100
PubChem Substance ID:
24877746
NACRES:
NA.22

concentration

80 wt. % in xylene

refractive index

n20/D 1.494

bp

97 °C

density

1.34 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

BrCC#C

InChI

1S/C3H3Br/c1-2-3-4/h1H,3H2

InChI key

YORCIIVHUBAYBQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

The product is an 80wt.% solution of propargyl bromide (3-bromo-1-propyne) in xylene.

Application

Propargyl bromide solution (80wt.% solution in xylene) may be used in the preparation of dimethyl 5-hydroxyisophthalate propargyl ether.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Oral - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT RE 2 Inhalation - STOT SE 3

Target Organs

Central nervous system,Liver,Kidney, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

45.0 °F - closed cup

Flash Point(C)

7.22 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

530409-125G:4548173166742
530409-VAR:
530409-BULK:
530409-50G:4548173166759

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

Customers Also Viewed

Slide 1 of 2

1 of 2

Allyl bromide ReagentPlus®, 99%, contains ≤1000 ppm propylene oxide as stabilizer

Sigma-Aldrich

A29585

Allyl bromide

Potassium tert-butoxide reagent grade, ≥98%

Sigma-Aldrich

156671

Potassium tert-butoxide

Self-assembly of amphiphilic polymeric dendrimers synthesized with selective degradable linkages.
Urbani CN, et al.
Macromolecules, 41(1), 76-86 (2008)
Francesco Alessandrini et al.
International immunopharmacology, 29(1), 105-109 (2015-06-03)
The involvement of muscarinic receptors in cancer has been reported. Recently we have demonstrated that the activation of M2 muscarinic receptors, through arecaidine propargyl ester, arrests cell proliferation and induces apoptosis in primary and established glioblastoma cell lines. Considering the
Maria Di Bari et al.
Neurochemistry international, 90, 261-270 (2015-10-13)
Glioblastomas are the most common brain tumors in humans. Previously, we demonstrated that the muscarinic receptor agonist, arecaidine propargyl ester, via M2 receptors, inhibits cell proliferation in a time and dose-dependent manner and induces a severe apoptosis in human U251
Jong Hwan Kwak et al.
Biomaterials, 61, 52-60 (2015-05-23)
We studied the blood-brain barrier (BBB) permeability and intracellular localization of a fluorescein isothiocyanate (FITC)-labeled dieckol (1) and a rhodamine B-labeled dieckol (7), for exploring the possible therapeutic application of fluorone-labeled dieckols in neurodegenerative diseases. Both compounds (1 &7) were
Abdelaziz Al Ouahabi et al.
Journal of the American Chemical Society, 137(16), 5629-5635 (2015-04-09)
Sequence-defined non-natural polyphosphates were prepared using iterative phosphoramidite protocols on a polystyrene solid support. Three monomers were used in this work: 2-cyanoethyl (3-dimethoxytrityloxy-propyl) diisopropylphosphoramidite (0), 2-cyanoethyl (3-dimethoxytrityloxy-2,2-dimethyl-propyl) diisopropylphosphoramidite (1), and 2-cyanoethyl (3-dimethoxytrityloxy-2,2-dipropargyl-propyl) diisopropylphosphoramidite (1'). Phosphoramidite coupling steps allowed rapid synthesis

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