Skip to Content
Merck
CN

112747

N-Acetylsulfanilyl chloride

98%

Synonym(s):

4-Acetamidobenzenesulfonyl chloride

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
4-(CH3CONH)C6H4SO2Cl
CAS Number:
Molecular Weight:
233.67
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-485-1
Beilstein/REAXYS Number:
746676
MDL number:
Assay:
98%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


assay

98%

mp

142-145 °C (dec.) (lit.)

functional group

amide

SMILES string

CC(=O)Nc1ccc(cc1)S(Cl)(=O)=O

InChI

1S/C8H8ClNO3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,11)

InChI key

GRDXCFKBQWDAJH-UHFFFAOYSA-N

General description

L-hydroxyproline has been derivatized with N-acetylsulfanilyl chloride and 5-chlorovaleric acid during the synthesis of the haptens HP1 and HP2.

Application

N-Acetylsulfanilyl chloride is used in the synthesis of N1,N1-dimethylsulfanilamide as the internal standard in the reaction. The reaction is used to determine tramadol and its O-desmethylated metabolite in blood plasma.


pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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