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Chloramben

CAS No.
133-90-4
Chemical Name:
Chloramben
Synonyms
AMBEN;AMIBEN;Amibin;Amoben;Naptol;Ambiben;Vegaben;Vegiben;Acpm-629;amibends
CBNumber:
CB5702082
Molecular Formula:
C7H5Cl2NO2
Molecular Weight:
206.03
MDL Number:
MFCD00065093
MOL File:
133-90-4.mol
MSDS File:
SDS
Last updated:2024-12-18 14:08:57

Chloramben Properties

Melting point 200 °C
Boiling point 312 °C
Density 1.4062 (rough estimate)
refractive index 1.6100 (estimate)
storage temp. 0-6°C
solubility Acetonitrile (Slightly), DMSO (Sparingly), Metahnol (Slightly)
pka 2.75±0.25(Predicted)
form Powder
color Pale Beige
Water Solubility 700 mg/L (25 ºC)
Merck 13,2082
BRN 2365906
Exposure limits An experimental carcinogen.
CAS DataBase Reference 133-90-4(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII EWG424FFB5
NIST Chemistry Reference 3-Amino-2,5-dichlorobenzoic acid(133-90-4)
Pesticides Freedom of Information Act (FOIA) Chloramben
EPA Substance Registry System Chloramben (133-90-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H319-H335-H350
Precautionary statements  P201-P302+P352-P305+P351+P338-P308+P313
Hazard Codes  T,Xn
Risk Statements  45-36/37/38-40
Safety Statements  53-22-26-36/37/39-45-36
RIDADR  UN 3077 9/PG 3
WGK Germany  3
RTECS  DG1925000
HS Code  29224999
Hazardous Substances Data 133-90-4(Hazardous Substances Data)
Toxicity Nontoxic to fish (Hartley and Kidd, 1987); acute oral LD50 for rats 5,620 mg/kg (Hartley and Kidd, 1987), 3,500 mg/kg (RTECS, 1985).
NFPA 704
0
2 0

Chloramben price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 152668 3-Amino-2,5-dichlorobenzoic acid 95% 133-90-4 5g $196.2 2024-03-01 Buy
Sigma-Aldrich 33392 Chloramben PESTANAL?, analytical standard 133-90-4 100mg $74.2 2022-05-15 Buy
TCI Chemical A1537 3-Amino-2,5-dichlorobenzoic Acid 133-90-4 5G $159 2024-03-01 Buy
TRC A605273 3-Amino-2,5-dichlorobenzoic acid 133-90-4 5g $185 2021-12-16 Buy
Biosynth Carbosynth FA70665 3-Amino-2,5-dichlorobenzoic acid 133-90-4 2g $50 2021-12-16 Buy
Product number Packaging Price Buy
152668 5g $196.2 Buy
33392 100mg $74.2 Buy
A1537 5G $159 Buy
A605273 5g $185 Buy
FA70665 2g $50 Buy

Chloramben Chemical Properties,Uses,Production

Description

Chloramben is a colorless, odorless, crystallinesolid. Molecular weight=206.03; Freezing/Meltingpoint=200-201℃; Vapor pressure=6.8 3 1023 mmHg at100℃. Hazard Identification (based on NFPA 704 MRating System): Health 3, Flammability 0, Reactivity 0.Soluble in water; solubility=690 ppm at 25℃.

Chemical Properties

Off-white to beige powder

Chemical Properties

Chloramben is a colorless, odorless, crystalline solid.

Uses

Chloramben may be used as an analytical reference standard for the determination of the analyte in water samples using liquid chromatography with electrochemical detection (LC-EC).

Uses

Preemergence or preplant herbicide used in many vegetable and field crops to control annual broad-leaved weeds and grasses. Also for postemergent control of common ragweed, redroot pigweed, smartweed and velvet-leaf.

Uses

Herbicide or plant growth regulator.

Definition

ChEBI: Chloramben is a chlorobenzoic acid.

General Description

Purplish white powder or light purple solid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Chloramben reacts with sodium hypochlorite solutions .

Health Hazard

ACUTE/CHRONIC HAZARDS: Chloramben emits toxic fumes when heated to decomposition.

Fire Hazard

Flash point data for Chloramben is not available, but Chloramben is probably combustible.

Agricultural Uses

Herbicide: A herbicide for grasses, and broadleaf weeds. Mostly used on soybeans, and also on corn, beans, asparagus, pumpkins, peanuts, sunflowers, peppers, cotton, sweet potatoes, squash, melons, hardwood trees, and some conifers. Not approved for use in EU countries. Not registered for use in the U.S. There are 51 global suppliers

Trade name

ACP-M-728®; AMBEN®; AMBIBEN®; AMIBEN®[C]; AMIBIN®; AMOBEN®; ORNAMENTAL WEEDER®[C]; VEGABEN®; VEGIBEN®[C]; WEEDONE® GARDEN WEEDER

Potential Exposure

A General Use Pesticide (GUP) that is no longer produced or sold in the United States. It is used as an herbicide for grasses, broadleaf weeds, soybeans, beans, and some vegetables. Workers involved in the manufacture, formulation, or application of this reemergence herbicide.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seekmedical attention immediately. If this chemical contactsthe skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove fromexposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing hasstopped and CPR if heart action has stopped. Transferpromptly to a medical facility. When this chemical hasbeen swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.

Environmental Fate

Soil. In soils, chloramben was degraded by microorganisms but no products were identified (Humburg et al., 1991). The main degradative pathway of chloramben in soil is decarboxylation and subsequent mineralization to carbon dioxide. The calculated halflives in Ella loamy sand, Kewaunee clay and Poygan silty clay were 120–201, 182–286 and 176–314 days, respectively (Wildung et al., 1968). Persistence in soil is 6–8 weeks (Hartley and Kidd, 1987).
Groundwater. According to the U.S. EPA (1986) and Ashton and Monaco (1991), chloramben has a high potential to leach to groundwater, especially in sandy soils during heavy rains. Plant. Degrades in plants to N-glucoside, glucose ester, conjugates and insoluble residues (Ashton and Monaco, 1991).
Photolytic. Plimmer and Hummer (1969) studied the irradiation of chloramben in water (2–4 mg/L) under a 450-W mercury vapor lamp (λ >2,800 ?) for periods of 2 to 20 hours. Chloride ion was released and a complex mixture of colored products was observed. It was postulated that amino free radicals reacted with each other via polymerization and oxidation processes. The experiment was repeated except the solution contained sodium bisulfite as an inhibitor under a nitrogen atmosphere. Oxidation did not occur and loss of the 2-chloro substituent gave 3-amino-5-chlorobenzoic acid (Plimmer and Hummer, 1969).
Chloramben (sodium salt) in aqueous solutions (100 mg/L) was rapidly photodegraded in outdoor sunlight and under a 360-W mercury arc lamp (Crosby and Leitis, 1969).
In sunlight, the solution became yellow-brown. Subsequent analysis by gas-liquid chromatography did not resolve any compounds other than chloramben. However, analysis by TLC indicated at least 12 unidentified products. These products were reportedly formed via replacement of chlorine by a hydroxy group, reductive dechlorination and abstraction of hydrogen from the amine group (oxidation). No photodegradation products could be identified in the solutions irradiated with the mercury arc lamp (Crosby and Leitis, 1969).
Chemical/Physical. Emits toxic fumes of nitrogen oxides and chlorine when heated to decomposition (Sax and Lewis, 1987). Forms water-soluble salts with alkalies.

Metabolism

Chloramben is generally stable to hydrolytic degradation; however, it will decompose in sodium hypochlorite solutions. It is also very sensitive to light and under oxidative conditions aqueous solutions will rapidly undergo photolysis. The predominant reaction in oxidative photolysis is unclear but appears to involve the formation of amino radicals. Photolysis also occurs under reductive conditions by dechlorination at the 2 position, i.e., when appropriate reducing agents are present, e.g., sodium bisulfite.

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with chloramben you should be trained on its proper handling and storage. Store in a cool, dry place, or a refrigerator, and avoidcontact with strong acids, acid fumes, and light. A regulated, marked area should be established where this chemical is handled, used, or stored in compliance with OSHAStandard 1910.1045.

Shipping

UN2588 Pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Toxicity evaluation

Although limited studies are available, those that have been conducted, for example, on cows and dogs, indicate that the majority of ingested chloramben is quickly excreted through the urine and feces and does not accumulate in tissues. An interesting interaction between caffeine and chloramben suggests that they can form an insoluble complex in the intestinal tract and thus decrease the amount of chloramben absorbed into the blood stream. The acute oral LD50 in rat is >5000 mg/kg.

Incompatibilities

Rapidly decomposed by light. Strong acids and acid fumes

Waste Disposal

Chloramben is stable to heat, oxidation, and hydrolysis in acidic or basic media. The stability is comparable to that of benzoic acid. Wet oxidation or incineration are recommended disposal methods.

Chloramben Preparation Products And Raw materials

Global( 126)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325 sales1@chuanghaibio.com China 5889 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22963 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32161 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
GLR Innovations
+91 9891111994 info@glrgroup.in India 4535 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49978 58
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 52924 58

View Lastest Price from Chloramben manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
chloramben pictures 2024-10-11 chloramben
133-90-4
US $0.00 / KG 1KG 99% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
  • chloramben pictures
  • chloramben
    133-90-4
  • US $0.00 / KG
  • 99%
  • Hebei Chuanghai Biotechnology Co,.LTD
2,5-Dichloro-3-aminobenzoic acid 2,5-dichloro-3-aminobenzoicacid 3-amino-2,5-dichloro-benzoicaci Acpm-629 ACP-M-728 Ambiben Amiben ds 3-AMINO-2,5-DICHLOROBENZOIC ACID AMBEN AMIBEN AMIBEN(R) CHLORAMBEN TIMTEC-BB SBB003492 3-AMINO-2,5-DICHLOROBENZOIC ACID,250MG,& CHLORAMBEN PESTANAL CHLORAMBEN PESTANAL (3-AMINO-2,5-DI-CHLO 3-Amino-2,5-Dichlorobenzoic chloramben (bsi,iso,ansi,wssa) 3-amino-2,5-dichlorobeznoc acid VEGIBEN(R) Amiben,Vegiben amibends Amibin Amoben Benzoic acid, 3-amino-2,5-dichloro- Chlorambed Chlorambene Kyselina 3-amino-2,5-dichlorbenzoova kyselina3-amino-2,5-dichlorbenzoova Naptol NCI-C00055 Ornamental weeder Ornamental weeder 4G ornamentalweeder ornamentalweeder4g Vegaben Vegiben 3-Amino-2,5-dichlorobenzoic acid,97% 3-Amino-2,5-dichlorobenzoic acid,90% Chloramben 100mg [133-90-4] 3-Amino-2.5-dichlorobenzoic acid 100mg [133-90-4] 3-Amino-2,5-dichlorobenzoic acid,Chloramben Chloramben 0.1 Chloramben @100 μg/mL in MeOH ChlorambenSolution,100mg/L,5ml ChlorambenSolution,100mg/L,1ml C11110000 Chloramben Chloramben 100 μg/ml Acetonitrile 133-90-4 H2NC6H2Cl2CO2H C7H5O2Cl2N Unnatural Amino Acid Derivatives Specialty Synthesis Peptide Synthesis Aromatic Amino Acids Chloro Halogenated Herbicides