1,2,4-TRIAZOLE

PRODUCT IDENTIFICATION

CAS NO. 288-88-0

EINECS NO. 206-022-9
FORMULA C2H3N3
MOL WT. 69.06

H.S. CODE

2933.99

TOXICITY

LD50 orl-rat 1000-2000 mg/kg

SYNONYMS Pyrrodiazole; 1H-1,2,4-Triazole; s-Triazole;
SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE solid in various forms with characteristic odour.
MELTING POINT 120 - 121 C
BOILING POINT

260 C (Decomposes)

SPECIFIC GRAVITY

 

SOLUBILITY IN WATER 125 g/100 ml at 20 C
pH 8 (10 g/l, H2O, 20 °C)

AUTOIGNITION

490 C

pKa 4.27 ( at 20 C)
log P 1.78 (Octanol-water)
VAPOR PRESSURE 0.603 (mmHg at 25 C)
HENRY'S LAW 1.53E-06 (atm-m3/mole at 25 C)
OH RATE 1.00E-13  at 25 C (Atmospheric)

NFPA RATINGS

 

REFRACTIVE INDEX

 

FLASH POINT

170 C

STABILITY

Stable under ordinary conditions

GENERAL DESCRIPTION & EXTERNAL LINKS

Triazole is one of a class of organic heterocyclic compounds containing a five-membered diunsaturated ring structure composed of three nitrogen atoms and two carbon atoms at nonadjacent positions. The simplest member of the Triazole family is triazole itself, white to pale yellow crystalline solids with a weak characteristic odor; soluble in water and alcohol, melts at 120 C, boils at 260 C. Triazole and its derivatives are used for biological activities such as antiviral, antibacterial, antifungal and antituberculous. 1,2,4-Triazole is used as an intermediate for phytosanitary, pharmaceutical, medicine and pesticide products, photoconductor, and copying systems

Wikipedia Linking: http://en.wikipedia.org/wiki/Triazole

Preparation of a nicotinamide nucleoside analog via enzymatic ribosidation of 1,2,4-triazole, Annulating agents for construction of bicyclic 1,2,4-triazole systems, Efficient synthesis of 3-hydroxymethyl-4-phenyl-1,2,4-triazole, Synthesis of selectively C-3 and N-4 substituted [1,2,4]-triazoles, Attempted ring addition to 3,5-dimethyl-1,2,4-triazole, Anions of 1-substituted-1,2,4-triazoles as nucleophiles, Annulation onto 1,2,4-triazole via a Michael-type reaction, Bicyclic ring systems from appropriately substituted triazoles, Solvent and counterion effects on the NMR of disubstituted triazoliums......... ( http://www.wellesley.edu/)

AN EASY AND DIRECT METHOD FOR THE SYNTHESIS OF 1,2,4-TRIAZOLE DERIVATIVES THROUGH CARBOXYLIC ACIDS AND HYDRAZINOPHTHALAZINE (http://quimicanova.sbq.org.br/)

SALES SPECIFICATION

APPEARANCE

White to Yellowish Crystal

CONTENT

95.0% min

MELTING POINT

117 C min

TRANSPORTATION
PACKING
40kgs in Bag
HAZARD CLASS  
UN NO.  
OTHER INFORMATION
European Hazard Symbols: XN C, Risk Phrases: 22-36-63, Safety Phrases: 36/37

EXAMPLES OF AZOLE FUNGICIDE

IMIDAZOLE

TRIAZOLE

FUNGICIDE

CAS RN

FUNGICIDE

CAS RN

Climbazole

38083-17-9

Amisulbrom

348635-87-0

Clotrimazole

23593-75-1

Azaconazole

60207-31-0

Cyazofamid

120116-88-3

Bitertanol

55179-31-2

Fenamidone

161326-34-7

Bromuconazole

116255-48-2

Fenapanil

61019-78-1

Cyproconazole

94361-06-5

Glyodin

556-22-9

Diclobutrazol

75736-33-3

Imazalil

35554-44-0

Difenoconazole

119446-68-3

Isovaledione

 

Diniconazole

83657-24-3

Oxpoconazole

134074-64-9

Diniconazole-M

83657-18-5

Pefurazoate

101903-30-4

Epoxiconazole

135319-73-2 or
or 106325-08-0

Triazoxide

72459-58-6

Etaconazole

60207-93-4

Triflumizole

99387-89-0

Fenbuconazole

114369-43-6

 

 

Fluotrimazole

31251-03-3

 

 

Fluquinconazole

136426-54-5

 

 

Flusilazole

85509-19-9

 

 

Flutriafol

76674-21-0

 

 

Furconazole

112839-33-5

 

 

Furconazole (cis)

112839-32-4

 

 

Hexaconazole

79983-71-4

 

 

Ipconazole

125225-28-7

 

 

Metconazole

125116-23-6

 

 

Myclobutanil

66246-88-6

 

 

Penconazole

66246-88-6

 

 

Propiconazole

60207-90-1

 

 

Prothioconazole

178928-70-6

 

 

Quinconazole

103970-75-8

 

 

Simeconazole

149508-90-7

 

 

Tebuconazole

107534-96-3

 

 

Tetraconazole

112281-77-3

 

 

Triadimefon

43121-43-3

 

 

Triadimenol

55219-65-3

 

 

Triazbutil

16227-10-4

 

 

Triticonazole

131983-72-7

 

 

Uniconazole

83657-22-1

 

 

Uniconazole-P

83657-17-4