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72-14-0

72-14-0 structure
72-14-0 structure
  • Name: Sulfathiazole
  • Chemical Name: sulfathiazole
  • CAS Number: 72-14-0
  • Molecular Formula: C9H9N3O2S2
  • Molecular Weight: 255.317
  • Catalog: API Synthetic anti-infective drugs Sulfonamides and synergists
  • Create Date: 2018-06-18 13:31:24
  • Modify Date: 2026-07-03 07:04:39
  • Sulfathiazole is an organosulfur compound that has been used as a short-acting sulfa drug.Target: AntibacterialSulfathiazole (20 μg/L) starts to be degraded between day 31 and day 38 in one of the two batch reactors containing different wastewater matrices. Sulfathiazole is degraded at a substantially faster rate than sulfamethoxazole or sulfamethazine in the nitrification process (S3) [1]. Recovery from spiked manure slurry samples is 64% for Sulfathiazole at pH 9. Sulfathiazole has acidity constant of pKa of 7.1and retention times (tR) of 7.8. S/N values for Sulfathiazole are above 100 at the 1 mg/kg level [2]. Sulfathiazole sorption to inorganic sorbents exhibits pronounced pH dependence consistent with sorbate speciation and sorbent charge properties. Sulfathiazole cations are most important for sorption to clay minerals, followed by neutral species [3].
Name sulfathiazole
Synonyms 4-Amino-N-(2-thiazolyl)benzenesulfonamide, N1-(2-Thiazolyl)sulfanilamide
2-Sulfanilamidothiazole
Sulfatiazol
2-(4-AMINOBENZENESULFONAMIDO)THIAZOLE
2-(PA-AMINOBENZENESULPHONAMIDO)THIAZOLE
Norsulfazole
Sulfathiozole
Sulfathiazole(form1)
Sulphanyl acid N-(thiazol-2-yl)amide
Ro 7
SULFATHIAZOLE VETRANAL (4-AMINO-N-(2-THI
SULFATHIAZOLE
USAF sn-9
Sulfanilamidothiazole
Sulphathiazole
Sulfavitina
N1-2-THIAZOLYLSULFANILAMIDE
usafsn-9
SULFATHIAZOLE FREE ACID
2-(P-AMINOBENZENESULFONAMIDO)THIAZOLE
N1-2-Thiazolylsulfanilamid
Sulzol
Retroid
4-AMINO-N-THIAZOL-2-YL-BENZENESULFONAMIDE
Thiacoccine
Thiozamide
M & B 760
2-(p-Aminobenzenesulphonamido)thiazole
4-AMINO-N-(1,3-THIAZOL-2-YL)BENZENESULFONAMIDE
Pregna-1,4,6-triene-3,20-dione, 6-chloro-, (9b,10a)
sulfathiazone
Thiasulfol
Sulfathiazole [-0]
2-Sulfanilamidothiazol
Neo-Strepsan
NY-2-THIAZOLYLSULFANILAMIDE
4-AMINO-N-2-THIAZOLYLBENZENESULFONAMIDE
Sulfocerol
Thiazamide
Sulfathiazole, Powder
Nl-2-Thiazolylsulfanilamide
EINECS 200-771-5
Sulfathiazole(form3)
LABOTEST-BB LT00114899
SULFATHIAZOLE,POWDER,PURIFIED
2-(SulfanilylaMido)thiazole
2090 R.P.
Sulfathiazole Solution, 100ppm
4-Amino-N​-thiazol-​2-ylidene​benzene-s​ulfonamid​e
Sulfathiazolum
2-Sulfonamidothiazole
Sulfathiazloe
SULFATHIAZOL
1,6-Dehydro-6-chlororetroprogesterone
N1-(2-THIAZOLY)SULFANILAMIDE
Wintrazole
N-2-THIAZOLYLSULFANILAMIDE
ASISCHEM D50978
4-Amino-N-(1,3-thiazol-2-yl)benzenesulfonamide
MFCD00005319
2-(Sulfanilylamino)thiazole
2-(4-Aminobenzenesulfonamido)thiazole 2-Sulfanilamidothiazole N-2-Thiazolylsulfanilamide
6-Chloro-1,6-dehydroretroprogesterone
2090 RP
Sulfanilamide, N1-4-thiazolin-2-ylidene
2090 R.P
2-Sulfathiazole
NORSULFAZOLE
Description Sulfathiazole is an organosulfur compound that has been used as a short-acting sulfa drug.Target: AntibacterialSulfathiazole (20 μg/L) starts to be degraded between day 31 and day 38 in one of the two batch reactors containing different wastewater matrices. Sulfathiazole is degraded at a substantially faster rate than sulfamethoxazole or sulfamethazine in the nitrification process (S3) [1]. Recovery from spiked manure slurry samples is 64% for Sulfathiazole at pH 9. Sulfathiazole has acidity constant of pKa of 7.1and retention times (tR) of 7.8. S/N values for Sulfathiazole are above 100 at the 1 mg/kg level [2]. Sulfathiazole sorption to inorganic sorbents exhibits pronounced pH dependence consistent with sorbate speciation and sorbent charge properties. Sulfathiazole cations are most important for sorption to clay minerals, followed by neutral species [3].
Related Catalog
References

[1]. Perez, S., P. Eichhorn, and D.S. Aga, Evaluating the biodegradability of sulfamethazine, sulfamethoxazole, sulfathiazole, and trimethoprim at different stages of sewage treatment. Environ Toxicol Chem, 2005. 24(6): p. 1361-7.

[2]. Haller, M.Y., et al., Quantification of veterinary antibiotics (sulfonamides and trimethoprim) in animal manure by liquid chromatography-mass spectrometry. J Chromatogr A, 2002. 952(1-2): p. 111-20.

[3]. Kahle, M. and C. Stamm, Time and pH-dependent sorption of the veterinary antimicrobial sulfathiazole to clay minerals and ferrihydrite. Chemosphere, 2007. 68(7): p. 1224-31.
Density 1.6±0.1 g/cm3
Boiling Point 479.5±47.0 °C at 760 mmHg
Melting Point 202.5ºC
Molecular Formula C9H9N3O2S2
Molecular Weight 255.317
Flash Point 243.8±29.3 °C
Exact Mass 255.013611
PSA 121.70000
LogP 0.05
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.704
Storage condition 0-6°C
Stability Stable. Incompatible with strong oxidizing agents.
Water Solubility Insoluble (<0.1 g/100 mL at 21 ºC)

CHEMICAL IDENTIFICATION

RTECS NUMBER :
WP2360000
CHEMICAL NAME :
Sulfanilamide, N(sup 1)-2-thiazolyl-
CAS REGISTRY NUMBER :
72-14-0
LAST UPDATED :
199701
DATA ITEMS CITED :
19
MOLECULAR FORMULA :
C9-H9-N3-O2-S2
MOLECULAR WEIGHT :
255.33
WISWESSER LINE NOTATION :
T5N CSJ BMSWR DZ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
250 mg/kg/23D-I
TOXIC EFFECTS :
Sense Organs and Special Senses (Eye) - conjunctive irritation Kidney, Ureter, Bladder - changes in tubules (including acute renal failure, acute tubular necrosis) Skin and Appendages - dermatitis, allergic (after systemic exposure)
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1250 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 :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1370 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Parenteral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1 gm/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 :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
4500 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 :
400 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 :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1450 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 :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
990 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 :
Parenteral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Tumorigenic - tumor types after systemic administration not seen spontaneously
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2310 mg/kg/2W-C
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Tumorigenic - tumor types after systemic administration not seen spontaneously
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Parenteral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Tumorigenic - tumor types after systemic administration not seen spontaneously
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
29400 mg/kg
SEX/DURATION :
male 6 week(s) pre-mating
TOXIC EFFECTS :
Reproductive - Fertility - male fertility index (e.g. # males impregnating females per # males exposed to fertile nonpregnant females)

MUTATION DATA

TYPE OF TEST :
Phage inhibition capacity
TEST SYSTEM :
Microorganism - not otherwise specified
DOSE/DURATION :
5 mg/L
REFERENCE :
JGMIAN Journal of General Microbiology. (Soc. for General Microbiology, Journal Sales, 62 London Rd., Reading, RG1 5AS, UK) V.1- 1947- Volume(issue)/page/year: 8,116,1953 *** REVIEWS *** TOXICOLOGY REVIEW JMSHAO Journal of the Mount Sinai Hospital (New York). (New York, NY) V.1-36, 1934-69. For publisher information, see MSJMAZ. Volume(issue)/page/year: 10,343,1943 *** OCCUPATIONAL EXPOSURE LIMITS *** OEL-RUSSIA:STEL 1 mg/m3 JAN 1993 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 80540 No. of Facilities: 178 (estimated) No. of Industries: 5 No. of Occupations: 9 No. of Employees: 3666 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - 80540 No. of Facilities: 349 (estimated) No. of Industries: 2 No. of Occupations: 4 No. of Employees: 3171 (estimated) No. of Female Employees: 1476 (estimated)
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases S26
RIDADR 3249
WGK Germany 2
RTECS WP2360000
Packaging Group III
Hazard Class 6.1(b)
HS Code 2935009090
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%
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