Skip to Content
Merck
CN

24008

2-Chlorobutyric acid

≥97.0% (GC)

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3CH2CHClCOOH
CAS Number:
Molecular Weight:
122.55
EC Number:
224-029-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1720944
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

RVBUZBPJAGZHSQ-UHFFFAOYSA-N

InChI

1S/C4H7ClO2/c1-2-3(5)4(6)7/h3H,2H2,1H3,(H,6,7)

SMILES string

CCC(Cl)C(O)=O

assay

≥97.0% (GC)

refractive index

n20/D 1.439

bp

90-92 °C/12 mmHg (lit.)

density

1.190 g/mL at 20 °C (lit.)

Application

2-Chlorobutyric acid was used in the synthesis of 2-hydroxy-5-hexenyl 2-chlorobutyrate ester.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

García et al.
Biochemical engineering journal, 5(3), 185-190 (2000-06-01)
An esterification process was developed for the direct synthesis of 2-hydroxy-5-hexenyl 2-chlorobutyrate ester from 2-chlorobutyric acid by using the epoxide 1,2-epoxy-5-hexene and Mucor miehei immobilised lipase as the biocatalyst in a batch reactor. The effect of temperature, catalyst concentration, and
Khatereh Bahrpaima et al.
Biomolecules, 9(8) (2019-08-23)
In this work, 1-carboxypropyled (1-CPRLS) and 5-carboxypentyled lignosulfonates (5-CPELS) were synthesized using 2-chlorobutanoic acid and 6-chlorohexanoic acid as carboxylate group donors via SN1 and SN2 mechanisms, respectively. 1-Carboxypropyl and 5-carboxypentyl lignosulfonates with the charge densities of -3.45 and -2.94 meq

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