피클로람

피클로람
피클로람 구조식 이미지
카스 번호:
1918-02-1
한글명:
피클로람
동의어(한글):
파이클로람;피클로람
상품명:
Picloram
동의어(영문):
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
분자식:
C6H3Cl3N2O2
포뮬러 무게:
241.46
MOL 파일:
1918-02-1.mol
MSDS 파일:
SDS

피클로람 속성

녹는점
200 °C (dec.)(lit.)
끓는 점
421℃
밀도
1.9163 (rough estimate)
굴절률
1.6770 (estimate)
인화점
>110°(230°F)
저장 조건
0-6°C
용해도
아세톤에 용해됨
물리적 상태
과립
산도 계수 (pKa)
4.1(at 25℃)
색상
흰색, 황갈색
수용성
420mg/L
최대 파장(λmax)
252nm(Phosphate buffer sol.)(lit.)
Merck
14,7397
BRN
479075
노출 한도
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 데이터베이스
1918-02-1(CAS DataBase Reference)
IARC
3 (Vol. 53) 1991
NIST
2-Pyridinecarboxylic acid, 4-amino-3,5,6-trichloro-(1918-02-1)
EPA
Picloram (1918-02-1)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36
안전지침서 26
유엔번호(UN No.) 3077
WGK 독일 2
RTECS 번호 TJ7525000
TSCA Yes
위험 등급 9
포장분류 III
HS 번호 2933399990
유해 물질 데이터 1918-02-1(Hazardous Substances Data)
독성 LD50 in rats, mice, rabbits, guinea pig, chickens, sheep, cattle (mg/kg): 8200, 2000-4000, 2000, 3000, 6000, >1000, >750 orally (Mullison)
기존화학 물질 KE-05-0123
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H412 장기적 영향에 의해 수생생물에 유해함 수생 환경유해성 물질 - 만성 구분 3 P273, P501
예방조치문구:
P273 환경으로 배출하지 마시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
0
2 0

피클로람 MSDS


4-Amino-3,5,6-trichloropicolinic acid

피클로람 C화학적 특성, 용도, 생산

개요

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.

화학적 성질

Picloram is a colorless powder. Chlorine odor.

용도

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.

일반 설명

Fine beige crystals or white powder. Odor of chlorine.

공기와 물의 반응

Insoluble in water.

반응 프로필

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.

건강위험

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.

화재위험

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

농업용

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).

상품명

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

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.

잠재적 노출

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

신진 대사

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.

운송 방법

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

비 호환성

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.

폐기물 처리

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.

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