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Trifluralin in Hexane - 1000μg/mL in Hexane, high purity , CAS No.1582-09-8

    Grade & Purity:
  • 1000μg/mL in Hexane
In stock
Item Number
BWY272997
Grouped product items
SKU Size
Availability
Price Qty
BWY272997-1.2ml
1.2ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$86.90

Basic Description

Synonyms trifluralin | 1582-09-8 | Treflan | 2,6-Dinitro-N,N-dipropyl-4-(trifluoromethyl)aniline | Agreflan | Elancolan | Crisalin | Triflurex | Trifurex | Tristar | Nitran | Nitran K | Trifluraline | Crisalina | Digermin | Synfloran | Trefanocide | Treficon | Trikepin | Ipersan | Olitref | Super-Treflan |
Specifications & Purity 1000μg/mL in Hexane
Storage Temp Store at 2-8°C,Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

This standard substance is mainly used for measuring instrument calibration, analysis method evaluation and quality control, as well as the content determination and residue detection of corresponding components in the fields of food, hygiene, environment and agriculture. It can also be used for value traceability or as a standard stock solution. Dilute and prepare various standard solutions for work.


Sample Preparation 

 

This standard material is made of trifluralin pure product with accurate purity as raw material, GC-grade n-hexane as solvent, and accurately prepared by weight-volume method.

Trifluralin (alias: Trifluralin), English name: Trifluralin, CAS: 1582-09-8

 

Traceability and valuation method

 

This standard material uses the prepared value as the standard value, and uses GC-MS to compare the batch of standard materials and quality control control samples to verify the prepared value. Through the use of preparation methods, measurement methods and measuring instruments that meet the requirements of metrological characteristics, the traceability of the value of the reference material is guaranteed.

 

Characteristic value and uncertainty

 

Number

Name

Standard value(μg/mL)

Relative expanded uncertainty(%)(k=2)

BWY272997

Trifluralin in Hexane

1000

3

 

The uncertainty of the standard value is mainly composed of raw material purity, weighing, constant volume, uniformity, stability and other uncertainty components.

 

Uniformity inspection and stability inspection

 

According to JJF1343-2012 [General Principles and Statistical Principles for Determining Standard Material Values], the samples after subpackage are randomly sampled, the solution concentration is tested for uniformity and stability. The results show that the standard material has good uniformity and stability.

The quality value of this standard material is valid for 24 months from the date of setting the value. The development unit will continue to track and monitor the stability of the standard material. If the value changes within the validity period, the user will be notified in time.

 

Packaging, transportation and storage, use and precautions

 

1. Packaging: This standard material is packaged in a borosilicate glass ampoule, about 1.2mL/piece, please refer to the pipette volume when pipetting or diluting.

2. Transportation and storage: ice bag transportation, avoid squeezing and collision during transportation; store under refrigerated and dark conditions.

3. Use: Equilibrate at room temperature (20±3℃) before unpacking and shake well. Once the ampoule is opened, it should be used immediately. It cannot be used as a standard substance after being sealed again.


Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Aniline and substituted anilines
Intermediate Tree Nodes Not available
Direct Parent Dinitroanilines
Alternative Parents Trifluoromethylbenzenes  Nitrobenzenes  Nitroaromatic compounds  Dialkylarylamines  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organofluorides  Organic oxides  Hydrocarbon derivatives  Alkyl fluorides  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Dinitroaniline - Trifluoromethylbenzene - Nitrobenzene - Nitroaromatic compound - Tertiary aliphatic/aromatic amine - Dialkylarylamine - C-nitro compound - Tertiary amine - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organofluoride - Organopnictogen compound - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alkyl halide - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as dinitroanilines. These are organic compounds containing an aniline moiety, which is substituted at 2 positions by a nitro group.
External Descriptors Dinitroaniline herbicides

Associated Targets(Human)

AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Homo sapiens (32628 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
THP-1 (11052 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania infantum (5912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cryptosporidium parvum (1150 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leishmania donovani (89745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Toxoplasma gondii (4585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Allium cepa (293 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
psbA Photosystem Q(B) protein (72 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
psaC Photosystem I iron-sulfur center (3 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trianthema (24 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Urochloa platyphylla (12 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Boerhavia erecta (24 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Portulaca oleracea (78 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Amaranthus dubius (24 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Malva sylvestris (32 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Digitaria (171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Corynandra viscosa (24 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cyperus (12 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sesamum indicum (40 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Poaceae (20 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Eleusine indica (140 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cyperus rotundus (46 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Amaranthus tuberculatus (84 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Chenopodiastrum murale (32 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Clonostachys rosea (54 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2,6-dinitro-N,N-dipropyl-4-(trifluoromethyl)aniline
INCHI InChI=1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3
InChIKey ZSDSQXJSNMTJDA-UHFFFAOYSA-N
Smiles CCCN(CCC)C1=C(C=C(C=C1[N+](=O)[O-])C(F)(F)F)[N+](=O)[O-]
Isomeric SMILES CCCN(CCC)C1=C(C=C(C=C1[N+](=O)[O-])C(F)(F)F)[N+](=O)[O-]
WGK Germany 2
RTECS XU9275000
UN Number 3077
Packing Group III
Molecular Weight 335.28
Beilstein 1893555
Reaxy-Rn 1893555
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1893555&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Flash Point(°F) 212℉
Flash Point(°C) 100°C
Melt Point(°C) 48.5-49°C
Molecular Weight 335.280 g/mol
XLogP3 5.300
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 5
Exact Mass 335.109 Da
Monoisotopic Mass 335.109 Da
Topological Polar Surface Area 94.900 Ų
Heavy Atom Count 23
Formal Charge 0
Complexity 392.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yuyue Zang, Na Hang, Jiale Sui, Senlin Duan, Wanning Zhao, Jing Tao, Songqing Li.  (2024)  Magnetic Persimmon Leaf Composite: Preparation and Application in Magnetic Solid-Phase Extraction of Pesticides in Water Samples.  MOLECULES,  29  (1): (45). 
2. Xiumin Yang, Junmin Wang, Guifen Chang, Cuihong Sun, Qiuhua Wu, Zhi Wang.  (2024)  Post-synthetic modification of covalent organic framework for efficient adsorption of organochlorine pesticides from cattle's milk.  FOOD CHEMISTRY,  439  (138182). 
3. Bin Li, Zhonggang Wang.  (2023)  Highly sensitive and recognizable detection for trifluralin with alkyl-decorated fluorescent porous polymers.  CHEMICAL ENGINEERING JOURNAL,  470  (144123). 
4. Xiaohuan Zang, Qingyun Chang, Hongda Li, Xiaoxian Zhao, Shuaihua Zhang, Chun Wang, Zhi Wang.  (2023)  Construction of a ringent multi-shelled hollow MIL-88B as the solid-phase microextraction fiber coating for the extraction of organochlorine pesticides.  SEPARATION AND PURIFICATION TECHNOLOGY,  304  (122350). 
5. Jie Li, Zhuo Wang, Jinqiu Li, Shuaihua Zhang, Yangjuan An, Lin Hao, Xiumin Yang, Chun Wang, Zhi Wang, Qiuhua Wu.  (2022)  Novel N-riched covalent organic framework for solid-phase microextraction of organochlorine pesticides in vegetable and fruit samples.  FOOD CHEMISTRY,  388  (133007). 
6. Zhuojun Yan, Jinni Liu, Congke Miao, Pinjie Su, Guiyue Zheng, Bo Cui, Tongfei Geng, Jiating Fan, Zhiyi Yu, Naishun Bu, Ye Yuan, Lixin Xia.  (2022)  Pyrene-Based Fluorescent Porous Organic Polymers for Recognition and Detection of Pesticides.  MOLECULES,  27  (1): (126). 
7. Yuan Huamei, Ruan Guihua, Chen Zhengyi, Zhang Wenjuan, Jiang Xiangqiong, Du Fuyou.  (2020)  A porous carbon absorbent based on high internal phase emulsion for separation and enrichment of trifluralin from soil.  MICROCHIMICA ACTA,  187  (2): (1-8). 
8. Fuyou Du, Lingshun Sun, Qiulian Zen, Wei Tan, Zhenfang Cheng, Guihua Ruan, Jianping Li.  (2019)  A highly sensitive and selective “on-off-on” fluorescent sensor based on nitrogen doped graphene quantum dots for the detection of Hg2+ and paraquat.  SENSORS AND ACTUATORS B-CHEMICAL,  288  (96). 

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