Tebuconazole | 107534-96-3

Tebuconazole Properties

Melting point	102-105°C
Boiling point	476.9±55.0 °C(Predicted)
Density	1.25
vapor pressure	1.7 x l0^-6 Pa (20 °C)
refractive index	1.5800 (estimate)
Flash point	100 °C
storage temp.	Sealed in dry,2-8°C
solubility	Chloroform: Slightly Soluble; Methanol: Slightly Soluble
pka	13.70±0.29(Predicted)
form	Solid
color	White to Almost white
Water Solubility	32 mg/L at 20 ºC
Merck	14,9092
Henry's Law Constant	7.0×10⁴ mol/(m³Pa) at 25℃, HSDB (2015)
Major Application	agriculture cleaning products cosmetics environmental food and beverages personal care
InChI	1S/C16H22ClN3O/c1-15(2,3)16(10-21,20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7,11-12,21H,8-10H2,1-3H3
InChIKey	PXMNMQRDXWABCY-UHFFFAOYSA-N
SMILES	CC(C)(C)C(CO)(CCc1ccc(Cl)cc1)n2cncn2
LogP	3.700
CAS DataBase Reference	107534-96-3(CAS DataBase Reference)
EWG's Food Scores	3
FDA UNII	401ATW8TRW
NIST Chemistry Reference	Tebuconazole(107534-96-3)
EPA Substance Registry System	Tebuconazole (107534-96-3)
UNSPSC Code	41116107
NACRES	NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)

GHS07,GHS08,GHS09

Signal word

Warning

Hazard statements

H302-H361d-H410

Precautionary statements

P201-P202-P264-P273-P301+P312-P308+P313

PPE

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Hazard Codes

Xn;N,N,Xn

Risk Statements

22-51/53-63

Safety Statements

2-22-36/37-61

RIDADR

UN 3077 9/PG 3

WGK Germany

3

RTECS

XZ4803270

HazardClass

9

PackingGroup

III

HS Code

29339900

Storage Class

11 - Combustible Solids

Hazard Classifications

Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Repr. 2

Hazardous Substances Data

107534-96-3(Hazardous Substances Data)

Toxicity

bird - domestic,LD50,oral,> 1gm/kg (1000mg/kg),Pesticide Manual. Vol. 9, Pg. 785, 1991.

REACH Registrations

Inactive

NFPA 704

	0
2		0

Tebuconazole price More Price(52)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich	43897	Tebuconazole certified reference material, TraceCERT^®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland	107534-96-3	50 mg	$222	2026-04-30	Buy
Sigma-Aldrich	32013	Tebuconazole PESTANAL	107534-96-3	250mg	$77.4	2026-04-30	Buy
Sigma-Aldrich	R690236	1-(4-CHLOROPHENYL)-4,4-DIMETHYL-3-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-3-PENTANOL Aldrich	107534-96-3	25mg	$172	2023-01-07	Buy
TCI Chemical	T2988	Tebuconazole	107534-96-3	1G	$99	2026-04-30	Buy
TCI Chemical	T2988	Tebuconazole	107534-96-3	5G	$339	2026-04-30	Buy

Product number	Packaging	Price	Buy
43897	50 mg	$222	Buy
32013	250mg	$77.4	Buy
R690236	25mg	$172	Buy
T2988	1G	$99	Buy
T2988	5G	$339	Buy

Tebuconazole Chemical Properties, Uses, Production

Description

Tebuconazole is a trazole fungicide. It is taken up by plants and transported within tissues. It is used as a seed dressing, which works effectively against various smut and bunt diseases of cereals. As foliar spray tebuconazole controls numerous phathogens such as rust species, powdery mildew, and scale in various crops. It is also used to control pests including yellow leaf spot, black spot, net blotch, and Scelerotinia rot.
Tebuconazole can be applied to control above mentioned diseases on cereals (including wheat, barley, oat, rye), grapes, peanuts, vegetables (onions and peas), bananas, sugarcane.

References

[1] http://sitem.herts.ac.uk/aeru/ppdb/en/Reports/610.htm
[2] Pesticide residues in food – 1994 Report sponsored jointly by FAQ and WHO
[3] https://www.efsa.europa.eu/en/efsajournal/pub/3485

Chemical Properties

White Solid

Uses

A triazole fungicide showing potential carcinogenicity

Uses

Fungicide.

Uses

Tebuconazole used as a seed dressing is effective against various smut and bunt diseases of cereals. Used as a spray it controls numerous pathogens in various crops: rust species, powdery mildew, Rhyncosporum secalis, Sqtoria spp., Pyrenophora spp., Fusarium spp. in cereals, Mycosphaerella spp. in bananas, Pucciniu spp. and Sclerufium roIfsii in peanuts.

Uses

Ergosterol biosynthesis inhibitor. Fungicide.

Definition

ChEBI: 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol is a tertiary alcohol that is pentan-3-ol substituted by a 4-chlorophenyl, methyl, methyl, and a 1H-1,2,4-triazol-1-ylmethyl at positions 1, 4, 4 and 3 respectively. It is a member of monochlorobenzenes, a member of triazoles and a tertiary alcohol.

Agricultural Uses

Fungicide, Plant growth regulator: Used as a seed treatment against smuts and bunts of cereals; as a foliar spray against diseases of cereal, peanuts, oilseed rape, grapes, bananas, stone fruit, and pome fruit. Registered for use in EU countries. Registered for use in the U.S.

Trade name

BAY®-HWG 1608; BAYER®-HWG-1608 CORAIL®; ELITE®; FOLICUR®; FOLITRAZOLE®; GAUCHO®; HORIZON®; HWG 1608®; LYNX-1.2®; PREVENTOL® RAXIL (tebuconazole + metalaxyl); SILVACUR®; TEBUJECT®; WOLMAN®; WOODLIFE®

Mechanism of action

Systemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor.

Synthesis

4H-1,2,4-Triazole-4-ethanol, α-[2-(4-chlorophenyl)ethyl]-α-(1,1-dimethylethyl)-

97821-63-1

107534-96-3

To a 250 mL three-necked flask was added 120 g of N,N-dimethylformamide, followed by 40 g of pentaconazole isomer, 2.0 g of potassium hydroxide, and 1.0 g of 3-bromomethyl-1-(4-chlorophenyl)-4,4-dimethyl-3-propanol.The reaction mixture was heated to 150 °C and maintained at this temperature for 4 hours. Sampling and analysis during the reaction showed that the purity of tebuconazole was 99.8% and the isomer content was 0.2%. Upon completion of the reaction, the target product tebuconazole was obtained by removing the solvent, followed by slurry treatment with water and toluene, and finally filtered to give 38.6 g of the target product tebuconazole in 96.5% yield and 98.5% product purity.

Metabolic pathway

Tebuconazole is degraded in soils and does not accumulate. In plants the metabolites were mainly compounds containing triazole, and in mammals tebuconazole was rapidly metabolised and excreted in urine and faeces.

Degradation

Tebuconazole is stable to elevated temperatures. Under sterile conditions it is stable to hydrolysis in water. It is hydrolysed slowly with a DTS0 of >1 year.
Only two products were formed by irradiation of a suspension of tebuconazole in water with UV light (>280 nm). These were the hydrochloride (3) and 1,2,4-triazole (2). The expected product in which chlorine was replaced by hydroxyl could not be isolated. In organic solvents a number of products were formed. Several products (3, 4, 5, 6, 7, 8, 9, 12, 13, 14) were isolated from benzene after 72 hours irradiation (>280 nm). In a number of cases products isolated from photolysis in benzene were formed by reactions in which the solvent participated and involved addition of a benzene molecule (4, 9, 5, 6). On irradiation in methylene chloride and methanol, 4-chloracetophenone (10) and acetophenone (11) were also identified in addition to starting material and 1,2,4-triazole (Wamhoff et al., 1994).

References

[1] Patent: CN106699675, 2017, A. Location in patent: Paragraph 0024-0026
[2] Patent: US4639527, 1987, A

Pesticide Type

Fungicide; Plant Growth Regulator

Tebuconazole synthesis

Synthesis of Tebuconazole from 4H-1,2,4-Triazole-4-ethanol, α-[2-(4-chlorophenyl)ethyl]-α-(1,1-dimethylethyl)-

Tebuconazole Preparation Products And Raw materials

Raw materials

Pinacolone Tebuconazole 1,2,4-Triazole 4H-1,2,4-Triazole-4-ethanol, α-[2-(4-chlorophenyl)ethyl]-α-(1,1-dimethylethyl)- 2-[2-(4-Chlorophenyl)ethyl]-2-(1,1-dimethylethyl)-oxirane

N,N-Dimethylformamide Potassium hydroxide

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Preparation Products

Seed coating

Tebuconazole Suppliers

Global Suppliers ( 539)

Supplier	Tel	Email	Country	ProdList	Advantage
0	18769832557 18769832557	3948893484@QQ.com	China	2977	58
Qingdao Frisenno Biotechnology Co., Ltd	13370813718 13370813718	3073008326@qq.com	China	706	58
Tai'an Xinrun Biotechnology Co., Ltd.	15318133072 15318133072	3699029519@qq.com	China	1883	58
J & K SCIENTIFIC LTD.	18210857532 18210857532	jkinfo@jkchemical.com	China	96815	76
TCI (Shanghai) Development Co., Ltd.	021-67121386	Sales-CN@TCIchemicals.com	China	24512	81
Beijing HwrkChemical Technology Co., Ltd	89508211 18501085097	sales.bj@hwrkchemical.com	China	9407	55
Rudong Zhongyi Chemical Co., Ltd	13306234115	jszyzj@zhongyichem.com	China	36	60
Shanghai Hanhong Scientific Co.,Ltd.	021-54306202 13764082696	info@hanhongsci.com	China	42917	64
Chemsky（shanghai）International Co.,Ltd.	021-50135380	shchemsky@sina.com	China	32273	50
Sichuan Kulinan Technology Co., Ltd	400-1166-196 18981987031	cdhxsj@163.com	China	11674	57

Supplier	Advantage
0	58
Qingdao Frisenno Biotechnology Co., Ltd	58
Tai'an Xinrun Biotechnology Co., Ltd.	58
J & K SCIENTIFIC LTD.	76
TCI (Shanghai) Development Co., Ltd.	81
Beijing HwrkChemical Technology Co., Ltd	55
Rudong Zhongyi Chemical Co., Ltd	60
Shanghai Hanhong Scientific Co.,Ltd.	64
Chemsky（shanghai）International Co.,Ltd.	50
Sichuan Kulinan Technology Co., Ltd	57

View Latest Price from Tebuconazole manufacturers

Update time	Product	Price	Min. Order	Purity	Supply Ability	Manufacturer
2026-07-14	Tebuconazole		100KG	98	200TONS	Qingdao Trust Agri Chemical Co.,Ltd
2026-07-14	Tebuconazole 107534-96-3	$48.00		99.21%	10g	TargetMol Chemicals Inc.
2026-05-28	Tebuconazole 107534-96-3	$5.00	10KG	99 %	10000kg	Hebei Chuanghai Biotechnology Co,.LTD

Tebuconazole
$0.00
98
Qingdao Trust Agri Chemical Co.,Ltd

Tebuconazole
107534-96-3
$48.00
99.21%
TargetMol Chemicals Inc.

Tebuconazole
107534-96-3
$5.00
99 %
Hebei Chuanghai Biotechnology Co,.LTD

Tebuconazole Spectrum

Tebuconazole(107534-96-3)¹HNMR

107534-96-3 (Tebuconazole) Related Search:

2-Ethoxyethanol Poly(dimethylsiloxane) Chlorodimethylphenylsilane Ethylparaben Dimethyl sulfone

Ethyl formate Ethyl acetate Trinexapac-ethyl N,N-Dimethylaniline Tebuconazole-d9

Hexaconazole N,N-Dimethylacetamide Dimethyl sulfoxide Ethanol Dimethicone

N,N-Dimethylformamide Isoxadifen-ethyl Tebuconazole-d9

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(+/-)-alpha-(2-(4-chlorophenyl)ethyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazol-1-ethanol LYNX Lynx 1.2 LYNX(R) MATADOR ELITE(R) FOLICUR folicur 1.2 ec FOLICUR (TM) GWG 1609 hwg 1608 HORIZON 1-(4-CHLOROPHENYL)-4,4-DIMETHYL-3-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-3-PENTANOL 7, (5&alpha -Methyl-cholest-5-en-3&beta 17-Iodo-androsta-5,16-diene-3&beta -[N,N-(4-Phenylurazole)]-3-O-tert-butyldimethylsilyl-chol-6-en-24-al-3&beta 8&alpha 17(20), (5&alpha -OL ~95% 2-Methyl-5&alpha -OL ETHYL ESTER 3-Methoxy-18-methyl-1,3,5(10)-estratrien-17&beta -Pregnane-3-one-20&alpha 3-Methoxy-7&alpha -methyl-estra-2,5(10)-dien-17&beta )-CHOLESTEN-9-19-CYCLO-4, 4, 14&alpha 24, (5&alpha -[N,N-(4-Phenylurazole)]-3&beta -O-tert-butyldimethylsilyloxy-chol-6-en-24-oic Acid Methyl Ester -Cholesta-7,24-diene-3&beta )-ESTREN-3&alpha 17-Methyl-5&alpha -androst-2-eno[2,3-d]isoxazol-17&beta 1-(4-chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-ylmethyl)-3-pentanol 1-(4-Chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol 97% )-23, 24-BISNOR-CHOLENIC ACID-3&alpha A-[2-(4-CHLOROPHENYL)ETHYL]-A-(1,1-DIMETHYLETHYL)-1H-1,2,4-TRIAZOLE-1-ETHANOL TERBUCONAZOLE TEBUCONAZOLE(R) RAXIL RAXIL(R) (+-)-lethyl) (rs)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1h-1,2,4-triazol-1-ylmethyl)pentan-3 (rs)-1-p-chlorophenyl-4,4-dimethyl-3-(1h-1,2,4-triazol-1-ylmethyl)pentan-3-o 1-dimethylethyl)-1h-1,2,4-triazole-alpha-(2-(4-chlorophenyl)ethyl)-alpha-( 1-ethanol (RS)1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Silvacur Tebuconazlole FOLICUR, 100MG, NEAT 2 3 4-TRICHLORONITROBENZENE PESTANAL & 1-(4-chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-ylmethyl)pentan-3-ol Tebuconazol, 1-(4-Chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)-3-pentanol Tebuconazole suspension （RS）-1-（4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazole-1-ylmethyl)pentan-3-ol HGW 1608 1H-1,2,4-Triazole-1-ethanol, .alpha.-2-(4-chlorophenyl)ethyl-.alpha.-(1,1-dimethylethyl)-