Benazolin

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 584129

CAS#: 3813-05-6

Description: Benazolin is a synthetically produced chemical compound from the group of thiazolinones (thiazolines with a keto group) or benzothiazolinones. The colorless, crystalline solid is used predominantly as a herbicide agent.

Chemical Structure

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Benazolin
CAS# 3813-05-6
Instruction

Theoretical Analysis

MedKoo Cat#: 584129
Name: Benazolin
CAS#: 3813-05-6
Chemical Formula: C9H6ClNO3S
Exact Mass: 242.98
Molecular Weight: 243.660
Elemental Analysis: C, 44.36; H, 2.48; Cl, 14.55; N, 5.75; O, 19.70; S, 13.16

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Benazolin; Asset; EX 10781; EX-10781; EX10781; Galipan; Galtak; Grassland weedkiller; Herbazolin; Herbitox; Keropur; Legumex Extra; Tillox

IUPAC/Chemical Name: 3-Benzothiazolineacetic acid, 4-chloro-2-oxo-

InChi Key: HYJSGOXICXYZGS-UHFFFAOYSA-N

InChi Code: InChI=1S/C9H6ClNO3S/c10-5-2-1-3-6-8(5)11(4-7(12)13)9(14)15-6/h1-3H,4H2,(H,12,13)

SMILES Code: O=C(O)CN1C(SC2=CC=CC(Cl)=C12)=O

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 243.66 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Liu X, Yang T, Hu J. Determination of benazolin-ethyl residues in soil and rape seed by SPE clean-up and GC with electron capture detection. J Chromatogr Sci. 2013 Jan;51(1):87-91. doi: 10.1093/chromsci/bms102. Epub 2012 Jun 19. PubMed PMID: 22718745.

2: Cai T, Qian L, Cai S, Chen L. Biodegradation of benazolin-ethyl by strain Methyloversatilis sp. cd-1 isolated from activated sludge. Curr Microbiol. 2011 Feb;62(2):570-7. doi: 10.1007/s00284-010-9746-7. Epub 2010 Sep 17. PubMed PMID: 20848105.

3: Berns AE, Schnitzler F, Drewes N, Vereecken H, Burauel P. Dynamics of benazolin under the influence of degrading maize straw in undisturbed soil columns. Environ Toxicol Chem. 2007 Oct;26(10):2151-7. PubMed PMID: 17867883.

4: Schnitzler F, Lavorenti A, Berns AE, Drewes N, Vereecken H, Burauel P. The influence of maize residues on the mobility and binding of benazolin: investigating physically extracted soil fractions. Environ Pollut. 2007 May;147(1):4-13. Epub 2007 Jan 18. PubMed PMID: 17240026.

5: Chingombe P, Saha B, Wakeman RJ. Effect of surface modification of an engineered activated carbon on the sorption of 2,4-dichlorophenoxy acetic acid and benazolin from water. J Colloid Interface Sci. 2006 May 15;297(2):434-42. Epub 2005 Dec 9. PubMed PMID: 16337952.

6: Séquaris JM, Lavorenti A, Burauel P. Equilibrium partitioning of (14)C-benzo(a)pyrene and (14)C-benazolin between fractionated phases from an arable topsoil. Environ Pollut. 2005 Jun;135(3):491-500. PubMed PMID: 15749546.

7: Kelly ID, Smith S. Chromatographic purification and identification of polar metabolites of benazolin-ethyl from soybean. Int J Environ Anal Chem. 1986;25(1-3):135-49. PubMed PMID: 3744655.