Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

588288

Sigma-Aldrich

1-Bromobutane-4,4,4-d3

98 atom % D

Synonym(s):

Butyl bromide-4,4,4-d3

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

About This Item

Linear Formula:
CD3(CH2)2CH2Br
CAS Number:
55724-42-0
Molecular Weight:
140.04
MDL number:
MFCD01073988
UNSPSC Code:
12352101
PubChem Substance ID:
329758491

isotopic purity

98 atom % D

bp

100-104 °C (lit.)

mp

-112 °C (lit.)

density

1.303 g/mL at 25 °C

mass shift

M+3

SMILES string

[2H]C([2H])([2H])CCCBr

InChI

1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3/i1D3

InChI key

MPPPKRYCTPRNTB-FIBGUPNXSA-N

Related Categories

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 2 - Carc. 2 - Flam. Liq. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 2 Inhalation - STOT SE 3

Target Organs

Liver, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

71.6 °F - closed cup

Flash Point(C)

22 °C - closed cup

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.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

588288-BULK:
588288-VAR:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
CC0699

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yohei Sakaguchi et al.
The Analyst, 140(6), 1965-1973 (2015-02-12)
We have developed a novel amino acid analysis method using derivatization of multiple functional groups (amino, carboxyl, and phenolic hydroxyl groups). The amino, carboxyl, and phenolic hydroxyl groups of the amino acids were derivatized with 1-bromobutane so that the hydrophobicities

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