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THIACETAZONE

CAS No.
104-06-3
Chemical Name:
THIACETAZONE
Synonyms
tbi;Thiosemicarbazone;Thioacetazone;TB 1;Tb I;Antib;Tibon;Tubin;A 4081;4207rp
CBNumber:
CB8422936
Molecular Formula:
C10H12N4OS
Molecular Weight:
236.29
MDL Number:
MFCD00022157
MOL File:
104-06-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-08 07:26:47

THIACETAZONE Properties

Melting point 225-230 °C
Density 1.2752 (rough estimate)
refractive index 1.6440 (estimate)
storage temp. Store at -20°C
solubility Soluble in DMSO
form powder to crystal
pka 11.35±0.70(Predicted)
color White to Orange to Green
EWG's Food Scores 1
NCI Dictionary of Cancer Terms TBI
FDA UNII MMG78X7SSR
ATC code J04AK07

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard Codes  Xn
Risk Statements  22
Safety Statements  36
WGK Germany  3
RTECS  AE3850000
HS Code  29309090
Toxicity LD50 s.c. in mice: 1-2 g/kg (Bavin)
NFPA 704
0
1 0

THIACETAZONE price More Price(47)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S725927 4-ACETAMIDOBENZALDEHYDE THIOSEMICARBAZONE AldrichCPR 104-06-3 1 unit $197 2026-04-30 Buy
Sigma-Aldrich S725927 4-ACETAMIDOBENZALDEHYDE THIOSEMICARBAZONE Aldrich 104-06-3 50mg $179 2024-03-01 Buy
TCI Chemical T3632 Thiacetazone >98.0%(HPLC) 104-06-3 250mg $65 2026-04-30 Buy
Cayman Chemical 34589 Thioacetazone ≥98% 104-06-3 100mg $36 2026-04-30 Buy
Cayman Chemical 34589 Thioacetazone ≥98% 104-06-3 500mg $120 2026-04-30 Buy
Product number Packaging Price Buy
S725927 1 unit $197 Buy
S725927 50mg $179 Buy
T3632 250mg $65 Buy
34589 100mg $36 Buy
34589 500mg $120 Buy

THIACETAZONE Chemical Properties, Uses, Production

Chemical Properties

Solid

Uses

Thiacetazone (cas# 104-06-3) is used in combination chemotherapy, in preparation of nucleosides as inhibitors of adenylate-forming enzyme MenE.

Definition

ChEBI: Thioacetazone is a member of acetamides and an anilide.

Indications

Thiacetazone is active against many strains of M. tuberculosis. It is not marketed in the United States. However, because of its low cost, it is used as a first-line agent in East Africa, especially in combination with compounds such as isoniazid. The most common side effects of thiacetazone include GI intolerance and development of rashes. It causes significant ototoxicity, especially when coadministered with streptomycin. Lifethreatening hypersensitivity reactions, such as hepatitis, transient marrow aplastic syndromes, neutropenia, and thrombocytopenia, have been reported.

Pharmaceutical Applications

Thioacetazone (USAN amithiozone) is a synthetic compound discovered during initial work on the sulfonamides, to which it is structurally related. It is only slightly soluble in water. It is a weak bacteristatic drug, with frequent serious side effects, particularly in HIV-positive persons to whom it must never knowingly be given. On the advice of the WHO it no longer has a place in the treatment of tuberculosis, except as a last resort in cases of extreme drug resistance.
In-vitro MICs vary considerably according to the medium used and bear little relation to in-vivo efficacy. Many strains of M. tuberculosis isolated in East Africa, India and Hong Kong are naturally more resistant than strains from Europe. Acquired resistance, as a result of monotherapy, is prevalent in the developing countries.
Thioacetazone is well absorbed, achieving a plasma concentration of 1–4 mg/L 2–4 h after a 100 mg oral dose. The plasma half-life is 8–12 h. Little is known about the distribution of the drug. Several metabolites are described. About 20% is eliminated in the urine; the fate of the remainder is unknown. Rashes are common, occurring in 2–4% of patients in Africa but much more frequently in those of Chinese ethnic origin. More severe skin reactions, exfoliative dermatitis and Stevens–Johnson syndrome occur in less than 0.5% of HIV-negative patients, but there is a 10-fold increase of these reactions in HIV-positive patients, proving fatal in up to 3% of such patients. Other common side effects include gastrointestinal reactions, vertigo and conjunctivitis. Less common reactions include hepatitis, erythema multiforme, hemolytic anemia and, rarely, agranulocytosis. Prolonged therapy may rarely lead to hypertrichosis, gynecomastia and osteoporosis. It is very rarely used, but may occasionally be considered (with other antituberculosis drugs) in extremely drug resistant tuberculosis.

THIACETAZONE Preparation Products And Raw materials

Raw materials

Preparation Products

THIACETAZONE Suppliers

Global Suppliers ( 138)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Adamas Reagent, Ltd. 400-6009262 15618770481 yhx@titansci.com China 14098 59
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2110 70
Spectrum Chemical Manufacturing Corp. 021-021-021-67601398-809-809-809 15221380277 marketing_china@spectrumchemical.com China 9643 60
T&W GROUP 021-61551611 13296011611 contact@trustwe.com China 9884 58
Thermo Fisher Scientific 800-810-5118 cnchemical@thermofisher.com China 17752 75
Beijing innoChem Science & Technology Co.,Ltd. 400-810-7969 010-59572699 ningzi.li@inno-chem.com.cn China 6122 55
Shanghai T&W Pharmaceutical Co., Ltd. +86 21 61551611 China 9874 58
TOKYO CHEMICAL INDUSTRY CO., LTD. 03-36680489 Sales-JP@TCIchemicals.com Japan 28364 80

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  • Mar 29,2022

View Latest Price from THIACETAZONE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Thiacetazone pictures 2026-07-07 Thiacetazone
104-06-3
$29.00 99.07% 10g TargetMol Chemicals Inc.
THIACETAZONE pictures 2019-12-26 THIACETAZONE
104-06-3
$1.00 1g ≥98% Career Henan Chemical Co

THIACETAZONE Spectrum

4’-formyl-acetanilid4’-(thiosemicarbazone) 4207 RP 4207rp A 4081 Acetamide, N-(4-(((aminothiomethyl)hydrazono)methylene)phenyl)- Acetamide, N-[4-[[(aminothioxomethyl)hydrazono]methyl]phenyl]- Acetamide, N1-(4-{[2-(aminocarbothioyl)hydrazono]methyl}phenyl) Acetanilide, 4'-formyl-, 4'-(thiosemicarbazone) Acetanilide, 4'-formyl-, thiosemicarbazone Aktivan Ambathizon Amithiozone Amitiozon Antib Benthiozone Benzothiozane Benzothiozon Berculon A berculona Berkazon CBC 903150 Conteben Diasan Diazan domagk’st.b.1conteben Domagk's t.b.1 conteben Domakol Ilbion Livazone magk’st.b.1conteben Magk'S T.B.1 conteben Mirizone neustab Mivizon Myvizone n-(4-(((aminothioxomethyl)hydrazono)methyl)phenyl)-acetamid N-(4-((E)-[2-(Aminocarbothioyl)hydrazono]methyl)phenyl)acetamide Neotibil Neustab Novakol Nuclon argentinian nuclonargentinian p-Acetamidobenzaldehyde thiosemicarbazon p-Acetamidobenzaldehyde thiosemicarbazone tb1(bayer) tbi/698 Tebalon Tebecure Tebemar Tebesone I tebesonei Tebethion Tebethione Tebezon Thiacetone Thiacetozone Thibon Thibone Thioacetazon