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Diazald

Names

[ CAS No. ]:
80-11-5

[ Name ]:
Diazald

[Synonym ]:
N,4-Dimethyl-N-nitrosobenzenesulfonamide
MFCD00002050
N-methyl-N-nitrosotoluene-p-sulfonamide
Benzenesulfonic acid, 4-methyl-, 1-methyl-2-oxohydrazide
EINECS 201-252-6
N-Methyl-N-nitroso-p-toluenesulfonamide
Diazald

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
320.5±35.0 °C at 760 mmHg

[ Melting Point ]:
~58 °C

[ Molecular Formula ]:
C8H10N2O3S

[ Molecular Weight ]:
214.242

[ Flash Point ]:
147.6±25.9 °C

[ Exact Mass ]:
214.041214

[ PSA ]:
75.19000

[ LogP ]:
0.58

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.573

[ Storage condition ]:
2-8°C

[ Stability ]:
Stable, but heat sensitive; may also be light sensitive. Incompatible with strong oxidizing agents, alkalies.

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
XT5950000
CHEMICAL NAME :
p-Toluenesulfonamide, N-methyl-N-nitroso-
CAS REGISTRY NUMBER :
80-11-5
BEILSTEIN REFERENCE NO. :
2214345
LAST UPDATED :
199701
DATA ITEMS CITED :
8
MOLECULAR FORMULA :
C8-H10-N2-O3-S
MOLECULAR WEIGHT :
214.26
WISWESSER LINE NOTATION :
ONN1&SWR D1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
2700 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
19 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
15 mg/kg
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Lungs, Thorax, or Respiration - tumors Blood - lymphoma, including Hodgkin's disease
TYPE OF TEST :
Specific locus test

MUTATION DATA

TYPE OF TEST :
Unscheduled DNA synthesis
TEST SYSTEM :
Rodent - rat Liver
DOSE/DURATION :
100 umol/L
REFERENCE :
ENMUDM Environmental Mutagenesis. (New York, NY) V.1-9, 1979-87. For publisher information, see EMMUEG. Volume(issue)/page/year: 3,11,1981

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H242-H315-H317-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves

[ Hazard Codes ]:
E:Explosive;Xi:Irritant;

[ Risk Phrases ]:
R2;R36/37/38;R43

[ Safety Phrases ]:
S15-S26-S35-S36/37

[ RIDADR ]:
UN 3234 4.1/PG 2

[ WGK Germany ]:
2

[ RTECS ]:
XT5950000

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1(b)

[ HS Code ]:
2935009090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2935009090

[ Summary ]:
2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

Articles

Anaerobic activation of p-cymene in denitrifying betaproteobacteria: methyl group hydroxylation versus addition to fumarate.

Appl. Environ. Microbiol. 80(24) , 7592-603, (2014)

The betaproteobacteria "Aromatoleum aromaticum" pCyN1 and "Thauera" sp. strain pCyN2 anaerobically degrade the plant-derived aromatic hydrocarbon p-cymene (4-isopropyltoluene) under nitrate-reducing c...

Diazald, a newly recognized antimicrobial agent and its spectrophotometric determination.

Acta Microbiol. Hung. 39(3-4) , 317-22, (1992)

Diazald, a chemical intermediate for the synthesis of biologically active compounds, was found to be a potent in vitro antimicrobial agent against yeasts, yeast-like and filamentous fungi as well as G...

Transnitrosating activity of N-nitroso-N-methyl-p-toluenesulfonamide in rats and human gastric juice.

Neoplasma 35(3) , 257-62, (1988)

N-nitroso-N-methyl-p-toluenesulfonamide (NMTS, diazald, CAS 80-11-5) is a widely used compound for laboratory production of diazomethane. The present results showed that the noncarcinogenic NMTS react...


More Articles


Related Compounds

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