ChemicalBook > CAS DataBase List > Picloram

Picloram

Product Name
Picloram
CAS No.
1918-02-1
Chemical Name
Picloram
Synonyms
PHYTIC ACID;PHYTOSTEROL;TORDON;4-AMINO-3,5,6-TRICHLOROPICOLINIC ACID;4-Amino-3,5,6-trichloro-2-picolinic acid;ATCP;Amdon;k-Pin;Grazon;TORDAN
CBNumber
CB8143725
Molecular Formula
C6H3Cl3N2O2
Formula Weight
241.46
MOL File
1918-02-1.mol
More
Less

Picloram Property

Melting point:
200 °C (dec.)(lit.)
Boiling point:
421℃
Density 
1.9163 (rough estimate)
refractive index 
1.6770 (estimate)
Flash point:
>110°(230°F)
storage temp. 
0-6°C
solubility 
Soluble in acetone
form 
Granules
pka
4.1(at 25℃)
color 
White, tan
Water Solubility 
420 mg/L
λmax
252nm(Phosphate buffer sol.)(lit.)
Merck 
14,7397
BRN 
479075
Exposure limits
OSHA PEL: 15 mg/m3 (total), 5 mg/m3 (respirable fraction); ACGIH TLV: TWA 10 mg/m3, STEL 20 mg/m3.
InChIKey
NQQVFXUMIDALNH-UHFFFAOYSA-N
LogP
0.300
CAS DataBase Reference
1918-02-1(CAS DataBase Reference)
NIST Chemistry Reference
2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro-(1918-02-1)
IARC
3 (Vol. 53) 1991
EPA Substance Registry System
Picloram (1918-02-1)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
RIDADR 
3077
WGK Germany 
2
RTECS 
TJ7525000
TSCA 
Yes
HazardClass 
9
PackingGroup 
III
HS Code 
2933399990
Hazardous Substances Data
1918-02-1(Hazardous Substances Data)
Toxicity
LD50 in rats, mice, rabbits, guinea pig, chickens, sheep, cattle (mg/kg): 8200, 2000-4000, 2000, 3000, 6000, >1000, >750 orally (Mullison)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
36774
Product name
Picloram
Purity
PESTANAL?, analytical standard
Packaging
250MG
Price
$120
Updated
2022/05/15
TCI Chemical
Product number
P1864
Product name
Picloram
Purity
>98.0%(HPLC)
Packaging
5g
Price
$90
Updated
2024/03/01
TCI Chemical
Product number
P1864
Product name
Picloram
Purity
>98.0%(HPLC)
Packaging
25g
Price
$223
Updated
2021/12/16
Alfa Aesar
Product number
J66702
Product name
Picloram, 95%
Packaging
5g
Price
$165
Updated
2024/03/01
Alfa Aesar
Product number
J66702
Product name
Picloram, 95%
Packaging
25g
Price
$602
Updated
2024/03/01
More
Less

Picloram Chemical Properties,Usage,Production

Description

Picloram is a colourless crystal. It is very soluble in acetone, ethanol, benzene, and dichloromethane. It is a systemic herbicide used for general woody plant control, sold under the trade names Tordon and Grazon. It also controls a wide range of broad-leaved weeds, but most grasses are resistant. It is used in formulations with other herbicides such as bromoxynil, diuron, 2,4-D, MCPA, triclorpyr, and atrazine. It is also compatible with fertilisers. Picloram, in the pyridine family of compounds, is a systemic herbicide used for control of woody plants and a wide range of broad-leaved weeds. Most grasses are resistant to picloram, so it is used in range management programs. Picloram is formulated either as an acid (technical product), a potassium or triisopropanolamine salt, or an isooctyl ester, and is available as either soluble concentrates, pellets, or granular formulations. The materials in this document refer to the technical acid form unless otherwise indicated. Picloram is stable under acidic, neutral and basic conditions. Picloram is formulated either as an acid (technical product), a potassium or triisopropanolamine salt, or an isooctyl ester, and is available as either soluble concentrates, pellets, or granular formulations and related manufacturing impurities.

Chemical Properties

Picloram is a colorless powder. Chlorine odor.

Uses

Herbicide.

Uses

Systemic herbicide used to control most broad-leaved weeds on grassland and noncrop areas. Use as a pesticide is restricted

Uses

It is used as a herbicide and defoliant.

Uses

Picloram is a dicot-selective, persistent herbicide and in salt form is used to control a variety of annual weeds on crops, perennial broadleaved herbs, and woody species in combination with 2,4-D or 2,4,5-T. It can persist in an active form in the soil from several months to years, and can also be released from the roots of treated plants into the soil, where other nontarget species may take it up and die. Picloram is of great use in the management of unwanted vegetation in rangeland, grass pastures, and forestry as well as non-cropland and rightsof- way sites, such as around industrial and military installations, roads, railways, airports, under power lines, and along pipelines. Additional uses in some countries include in rice, sugarcane, cereals, and oilseed rape.

Definition

ChEBI: Picloram is a pyridinemonocarboxylic acid that is pyridine-2-carboxylic acid which is substituted by a chloro group at positions 3,5 and 6, and by an amino group at position 4. It is a systemic herbicide used to control deeply rooted herbaceous weeds and woody plants in rights-of-way, forestry, range lands, pastures, and small grain crops. It has a role as a herbicide and a synthetic auxin. It is an aminopyridine, a pyridinemonocarboxylic acid, a chloropyridine and an organochlorine pesticide. It is functionally related to a picolinic acid.

General Description

Fine beige crystals or white powder. Odor of chlorine.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Picloram may be sensitive to prolonged exposure to light. Aqueous solutions may be decomposed by light. Picloram is incompatible with strong oxidizing agents, strong acids, acid chlorides and acid anhydrides.

Health Hazard

The toxic effects from ingestion or inhalation of dusts of picloram in test animals were mild. The acute oral LD50 values inrats and rabbits are 2900 and 2000 mg/kg,respectively. Maternal toxicity in rats wasobserved at a dose level of 750 mg/kg/day.Oral administration of picloram in rats andmice caused tumors in thyroid and liver.

Fire Hazard

Flash point data for Picloram are not available; however, Picloram is probably combustible.

Agricultural Uses

Herbicide: Picloram is a systemic herbicide used for control of woody plants and a wide range of broad-leaved weeds along roads, power lines and long right-of-ways. Most grasses are resistant to picloram, so it is used in range management programs to control noxious weeds and brush. It is used to prepare sites for tree planting. Picloram is formulated either as an acid (technical product), a potassium or triisopropanolamine salt, or an isooctyl ester, and is available as either soluble concentrates, pellets, or granular formulations. During the Vietnam war, a herbicide named Agent White was used to control vegetation. It was a mixture of 2,4-D, triisopropanolamine salt and picloram. A U.S. EPA restricted Use Pesticide (RUP).

Trade name

ACCESS®; AMDON®; AMDON GRAZON®; BOROLIN®; GRAZON® Picloram; K-PIN®; PATHWAY®; TORDON®[C]; TORDON® 101 MIXTURE; TORDON® 10 K; TORDON® 22 K

Biochem/physiol Actions

Picloram (4-Amino-3,5,6-trichloropyridine-2-carboxylic acid) is a chlorinated systemic herbicide widely used for woody plant and broad-leaved weed control. Picloram induces direct somatic embryogenesis of Lilium longiflorum var. Ceb-dazzel.

Safety Profile

Moderately toxic by ingestion. Questionable carcinogen with experimental carcinogenic, neoplas tigenic, tumorigenic, and teratogenic data. An experimental teratogen. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx.

Potential Exposure

A potential danger to those involved in the manufacture, formulation or application of this herbicide.

Environmental Fate

Soil. Degrades in soil via cleavage of the chlorine atom at the m-position to form 4- amino-5,6-dichloro-2-picolinic acid. Replacement of the chlorine at the m-posi-tion by a hydroxyl group yields 4-amino-3-hydroxy-5,6-dichloropicolinic acid (Hartley and Kidd, 1987). Other soil metabolites reported include carbon dioxide, chloride ions, 4-amino-6- hydroxy-3,5-dichloropicolinic acid (Meikle et al., 1974), 4-amino-3,5-dichloro-6-hydroxypicolinic acid and 4-amino-3,5,6-trichloropyridine (Goring and Hamaker, 1971). Youngson et al. (1967) reported that degradation increased with an increase in temperature and organic matter
The half-lives for picloram in soil incubated in the laboratory under aerobic conditions ranged from 29 days to 3 years with an average of 201 days (Meikle et al., 1973; Yoshida and Castro, 1975; Merkle et al., 1976). In field soils, the half-lives for pi
Groundwater. According to the U.S. EPA (1986) picloram has a high potential to leach to groundwater.
Plant. Picloram degraded very slowly in cotton plants releasing carbon dioxide (Meikle et al., 1966). Metabolites identified in spring wheat were 4-amino-2,3,5-trichloropyridine, oxalic acid and 4-amino-3,5-dichloro-6-hydroxypicolinic acid (Redemann et al., 1968; Plimmer, 1970). In soil, 4-amino-3,5-dichloro-6-hydroxypicolinic acid was the only compound positively identified (Redemann et al., 1968)
Photolytic. The sodium salt of picloram in aqueous solution was readily decom-posed by UV light (λ = 300–380 nm). Two chloride ions were formed for each molecule of picloram that reacted. It was postulated that degradation proceeded via a free ra

Metabolism

Chemical. Picloram is generally stable to hydrolytic degradation but will decompose in hot, concentrated alkali solutions. It undergoes photodecomposition when irradiated with UV light and, to a lesser extent, with sunlight. Degradation via photolysis is thought to primarily involve cleavage of the ring structure and liberation of substituent chlorine atoms producing oxamic acid and 3-oxo-β-alanine. Decarboxylation is not thought to be a major pathway in photolytic degradation.
Plant. Hall et al. (16) have shown that in rapeseed plants (Brassica spp.) >25% of picloram is metabolized 24 hours after treatment.
Soil. There is only limited microbial degradation in the soil. If picloram remains on the soil surface, it may undergo photolysis.

Shipping

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

Toxicity evaluation

Mammalian Toxicity. Studies conducted on dog, rat, steer, and human males indicate that most, if not all, of orally administered picloram is quickly excreted unmodified in the urine. The acute oral LD50s for male rat, mice, rabbit, guinea pig, sheep, and cattle are >5000, 2000–4000, ca. 2000, ca. 3000, >1000, and >750 mg/kg, respectively.
Weed Resistance/Modified Crop Tolerance. Weed resistance to picloram has been reported in populations of yellow starthistle (Centaurea solstitialis) (48) and wild mustard (Sinapis arvensis) (34). No crops with modified tolerance toward picloram are currently in production.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water and a salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur). This material is acidic. Reacts with hot concentrated alkali (hydrolyzes), strong bases. May attack metals.

Waste Disposal

This chlorinated brush killer is usually formulated with 2,4-D and the disposal problems are similar. Incineration @ 1000C for 2 seconds is required for thermal decomposition. Alternatively, the free acid can be precipitated from its solutions by addition of a mineral acid. The concentrated acid can then be incinerated and the dilute residual solution disposed in an area where several years’ persistence in the soil can be tolerated.

Picloram Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Picloram Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40240
Advantage
62
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9664
Advantage
60
Wuhan Fortuna Chemical Co., Ltd
Tel
027-027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2893
Advantage
58
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4941
Advantage
60
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Chengdu Forest Science and Technology Development Co., Ltd.
Tel
028-87925786 18030648795
Fax
028-61777050
Email
sales@cdforestchem.com
Country
China
ProdList
1379
Advantage
58
Shanghai civi chemical technology co.,Ltd
Tel
86-21-34053660
Fax
86-21-34053661
Email
sale@labgogo.com
Country
China
ProdList
9872
Advantage
52
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
Shanghai Jian Chao Chemical Technology Co., Ltd.
Tel
18017383231 18017383231
Fax
qq:2817624287
Email
lyh_antaeus@163.com
Country
China
ProdList
9352
Advantage
55
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
18521735133 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25015
Advantage
65
The future of Shanghai Industrial Co., Ltd.
Tel
021-61552785
Fax
021-55660885
Email
sales@shshiji.com
Country
China
ProdList
9552
Advantage
55
Nanjing Dulai Biotechnology Co., Ltd.
Tel
025-84699383-8003 18013301590
Fax
025-84699383-8003
Email
njduly@126.com
Country
China
ProdList
973
Advantage
55
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4428
Advantage
55
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3750
Advantage
55
TianJin Alta Scientific Co., Ltd.
Tel
022-65378550-8551
Fax
+86-022-2532-9655
Email
contact@altascientific.com
Country
China
ProdList
2773
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Finetech Industry Limited
Tel
027-87465837 19945049750
Fax
027-8777-2287
Email
sales@finetechnology-ind.com
Country
China
ProdList
9636
Advantage
58
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15878
Advantage
55
SHANGHAI BANGCHENG CHEMICAL Co.,Ltd.
Tel
021-69106960 13701823733
Fax
021-69106780
Email
13701823733@163.com
Country
China
ProdList
4775
Advantage
60
Hangzhou J&H Chemical Co., Ltd.
Tel
+86-571-87396432
Fax
0571-87396431
Email
sales@jhechem.com
Country
China
ProdList
10015
Advantage
53
Beijing Holiyang Chemical Co. Ltd.
Tel
13718199399
Fax
QQ : 206661479
Email
holiyangchem@163.com
Country
China
ProdList
3387
Advantage
56
Shanghai YouPeng Chemical Co. Ltd.
Tel
021-69005955 13701776567
Fax
021-69005775
Email
youpengchem@163.com
Country
China
ProdList
4303
Advantage
56
Sichuan Hainuowei Technology Co. Ltd.
Tel
13708085536
Fax
QQ : 121102042
Email
hanovichem@163.com
Country
China
ProdList
3389
Advantage
56
Shanghai TongYuan Chemical Co., Ltd.
Tel
021-021-69182866 13701855675
Fax
021-69182022
Email
tongyuanchem@126.com
Country
China
ProdList
4331
Advantage
58
Shanghai Kaisai Chemical Co., Ltd
Tel
021-33516722 13701817765
Fax
021-33516776
Email
kaisaichem@163.com
Country
China
ProdList
4751
Advantage
58
Shanghai LanRun Chemical Co., Ltd.
Tel
021-69515658 ; 69515628 13701998368
Fax
021-69515998
Email
longrunchem@163.com
Country
China
ProdList
3920
Advantage
50
Shanghai Rolead Chemical Technology Co., Ltd.
Tel
021-69992220 13701886816
Fax
021-69992237
Email
roleadchem@163.com
Country
China
ProdList
4759
Advantage
50
Shanghai Kangtuo Chemical Co., Ltd.
Tel
021-69185552 13701777608
Fax
021-69186006
Email
kangtuochem@163.com
Country
China
ProdList
4369
Advantage
55
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Alta Scientific Co., Ltd.
Tel
022-6537-8550 15522853686
Fax
022-2532-9655
Email
sales@altasci.com.cn
Country
China
ProdList
4515
Advantage
55
Hubei Kangbaotai Finechem Co., Ltd.
Tel
+86 (27) 8778653
Fax
+86 (27) 8773-8652
Email
13720228325@163.com
Country
China
ProdList
337
Advantage
58
Shanghai Synchem Pharma Co., ltd
Tel
021-61984905-1 18016477331
Email
synchempharma@aliyun.com
Country
China
ProdList
6455
Advantage
55
Chemwill Asia Co.,Ltd.
Tel
86-21-51086038
Fax
86-21-51861608
Email
sales@chemwill.com
Country
China
ProdList
1975
Advantage
58
Shanghai XiZhi Chemical Co., Ltd.
Tel
021-69005855 13701817869
Fax
021-69005955
Email
xizhichem@163.com
Country
China
ProdList
3341
Advantage
55
Shanghai Pengsuo Biochemical Technology Co., Ltd.
Tel
021-59118555 13701823997
Fax
021-59119222
Email
pengsuochem@163.com
Country
China
ProdList
3302
Advantage
55
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20810
Advantage
60
Raw material medicin reagent co.,Ltd
Tel
025-57798860
Email
sales@njromanme.com
Country
China
ProdList
4534
Advantage
58
Chengdu Dianchun Technology Co., Ltd
Tel
400-1166-196 18502815961
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
14623
Advantage
60
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Shenzhen Sendi Biological Technology Co., Ltd.
Tel
18124570582 TEL:0755-23574479 2355327139
Fax
0755-23229476 QQ: 2355327139
Email
siliao02@yccreate.com
Country
China
ProdList
6120
Advantage
58
Guangzhou Jhd Chemical Reagent Co., Ltd.
Tel
020-84383047
Fax
020-84380294
Email
sales@jhd.com.cn
Country
China
ProdList
9190
Advantage
65
Shanghai Orgchem Co.,Ltd.
Tel
+86-21-5877 1921
Fax
+86-21-5877 1925
Email
info@chemofchina.com
Country
China
ProdList
9661
Advantage
55
JinJin Le Chemical Co., Ltd
Tel
10106090
Email
jjlchem2@163.com
Country
China
ProdList
9986
Advantage
58
Shandong Ono Chemical Co., Ltd.
Tel
0539-6362799 20)
Fax
0539-6362799(To 20)
Country
China
ProdList
10007
Advantage
58
More
Less

View Lastest Price from Picloram manufacturers

Hebei Mojin Biotechnology Co., Ltd
Product
Picloram 1918-02-1
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-06-20
Hebei Mingeng Biotechnology Co., Ltd
Product
Picloram 1918-02-1
Price
US $200.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000kg/Month
Release date
2022-11-20
Hebei Guanlang Biotechnology Co., Ltd.
Product
Picloram 1918-02-1
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2021-08-13

1918-02-1, PicloramRelated Search:


  • RARECHEM AL BO 1809
  • PICLORAM
  • OTAVA-BB BB5110090065
  • 4-aminotrichloropicolinicacid
  • IFLAB-BB F3055-0927
  • PICLORAM, 250MG, NEAT
  • 4-AMINO-3,5,6-TRICHLOROPICOLINIC ACID, T ECH.
  • PICLORAM PESTANAL (4-AMINO-3,5,6-TRICHLO
  • PICLORAM[4-AMINO-3,5,6-TRICHLOROPYRIDINE-2-CARBOXYLICACID ]
  • Amdon
  • Amdon grazon
  • amdongrazon
  • ATCP
  • Borolin
  • Chloramp
  • Grazon
  • k-Pin
  • NCI-C00237
  • Piclorame
  • Picolinic acid, 4-amino-3,5,6-trichloro-
  • Tordon 101 mixture
  • Tordon 10K
  • Tordon 22K
  • AKOS BBS-00001392
  • 4-Amino-3,5,6-trichloro-2-picolinic acid
  • 4-AMINO-3,5,6-TRICHLOROPICOLINIC ACID
  • 4-AMINO-3,5,6-TRICHLOROPYRIDINE-2-CARBOXYLIC ACID
  • picloram plant cell culture tested
  • 3,5,6-Trichloro-4-Aminopicolinic acid
  • 3,5,6-trichloro-4-aminopicolinicacid
  • 4-Amino-3,5,6-trichloro-2-pyridine carboxylic acid
  • 4-amino-3,5,6-trichloro-2-pyridinecarboxylicaci
  • 4-amino-3,5,6-trichloro-picolinicaci
  • 4-Amino-3,5,6-trichlorpicolinsaeure
  • 4-amino-3,5,6-trichlorpicolinsaeure[german]
  • 4-Aminotrichloropicolinic acid
  • TIMTEC-BB SBB000816
  • TORDON
  • TORDON(R)
  • 2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro-
  • picloram (bsi,iso,ansi,wssa,jmaf)
  • TORDAN
  • PICHLORAM
  • TORDON75D
  • PHYTIC ACID
  • PHYTOSTEROL
  • 4-Amino -3,5,6-trichloro-2-picolinic acid - Total dust
  • 4-Amino -3,5,6-trichloro-2-picolinic acid- respirable dust
  • 4-Amino-3,5,6-trichloropicolinic acid, 4-Amino-3,5,6-trichloropyridine-2-carboxylic acid, Picloram
  • 4-Amino-3,5,6-trichloropicolinic acid, Picloram
  • 4-azanyl-3,5,6-trichloro-pyridine-2-carboxylic acid
  • 3,5,6-trichloro-4-aMinopyridine-2-carboxylic acid
  • 4-Amino-3,5,6-trichloropicolinic Acid 4-Amino-3,5,6-trichloropyridine-2-carboxylic Acid
  • 4-Amino-3,5,6-trichloro-2-pyridinecarboxylic acid (9CI)
  • Picloram Solution, 1000ppm
  • Picloram&gt
  • Picloram@0.1 mg/mL in Acetonitrile
  • Picloram @1000 μg/mL in Acetonitrile