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6310-29-8

2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid, also known as DCPTA, is a synthetic plant growth regulator belonging to the benzoic acid family. It is characterized by its four chlorine atoms and a diethylcarbamoyl group attached to the benzene ring. DCPTA functions by inhibiting the action of auxin, a plant hormone that regulates growth and development. This potent chemical has demonstrated its ability to enhance the yield and quality of various agricultural crops, making it a valuable asset for farmers and horticulturists.
Used in Agricultural Industry:
2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid is used as a plant growth regulator for promoting lateral branching and increasing fruit set in crops. It achieves this by inhibiting the action of auxin, which in turn enhances the yield and quality of the crops.

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  • 6310-29-8 Structure

  • Basic information

    1. Product Name: 2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid
    2. Synonyms: 2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid
    3. CAS NO:6310-29-8
    4. Molecular Formula: C12H11Cl4NO3
    5. Molecular Weight: 359.03
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6310-29-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 533.4°C at 760 mmHg
    3. Flash Point: 276.4°C
    4. Appearance: /
    5. Density: 1.508g/cm3
    6. Vapor Pressure: 3.3E-12mmHg at 25°C
    7. Refractive Index: 1.59
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 1.26±0.50(Predicted)
    11. CAS DataBase Reference: 2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid(6310-29-8)
    13. EPA Substance Registry System: 2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid(6310-29-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6310-29-8(Hazardous Substances Data)

6310-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6310-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6310-29:
(6*6)+(5*3)+(4*1)+(3*0)+(2*2)+(1*9)=68
68 % 10 = 8
So 6310-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H11Cl4NO3/c1-3-17(4-2)11(18)5-6(12(19)20)8(14)10(16)9(15)7(5)13/h3-4H2,1-2H3,(H,19,20)

6310-29-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5-tetrachloro-6-(diethylcarbamoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names Tetrachlor-phthalsaeure-mono-diethylamid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6310-29-8 SDS

6310-29-8Relevant articles and documents

The Chemistry of Azides derived from N-substituted Phthalamic and Tetrahalogenophthalamic Acids

Au, Ting Keung,Baydar, Ahmet E.,Boyd, Gerhard V.

, p. 2884 - 2889 (2007/10/02)

Treatment of eight phthalisoimidium perchlorates with sodium azide gave N-substituted o-carbamoylbenzoyl azides (2), which yielded o-carbamoylphenyl isocyanates (4) when heated.The isocyanates derived from tertiary phthalamic acids formed 4-dialkyl ammonio-1,4-dihydro-2H-3,1-benzoxazin-2-one perchlorates (8) by the action of perchloric acid and acetic anhydride; those containing secondary amide groups cyclised to 3-alkyl-quinazoline-2,4-(1H,3H)-diones (11) at rates depending on the size of the alkyl radicals.Tetrachloro- and tetrabromo-phthalic anhydride reacted with amines to yield the corresponding amic acids, their salts, of N-substituted 3-amino-4-hydroxyphthalides.Ring-chain isomerism was also observed in the case of the azides derived from two tertiary tetrachlorophthalamic acids.

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