티디아주론

티디아주론
티디아주론 구조식 이미지
카스 번호:
51707-55-2
한글명:
티디아주론
동의어(한글):
티디아주론;1-페닐-3-3(1,2,3-시아디아졸-5-일)우레아
상품명:
Thidiazuron
동의어(영문):
TDZ;Thiadiazuron;Thidiazurone;Lift;DROPP;defolit;sn49537;Avguron;DROPP(R);Dropp SC
CBNumber:
CB3684289
분자식:
C9H8N4OS
포뮬러 무게:
220.25
MOL 파일:
51707-55-2.mol
MSDS 파일:
SDS

티디아주론 속성

녹는점
213°C
밀도
1.3493 (rough estimate)
굴절률
1.6390 (estimate)
저장 조건
Sealed in dry,2-8°C
용해도
DMSO에 용해됨
산도 계수 (pKa)
12.06±0.70(Predicted)
Merck
13,9384
BRN
1078092
InChIKey
HFCYZXMHUIHAQI-UHFFFAOYSA-N
CAS 데이터베이스
51707-55-2(CAS DataBase Reference)
EPA
Thidiazuron (51707-55-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,N
위험 카페고리 넘버 36/37/38-51/53
안전지침서 22-26-36-61
유엔번호(UN No.) UN 3077 9 / PGIII
WGK 독일 3
RTECS 번호 YU1395000
HS 번호 2934999090
유해 물질 데이터 51707-55-2(Hazardous Substances Data)
독성 LC50 (96-hour) for bluegill sun?sh, channel cat?sh and rainbow trout >1,000 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats >5,000 mg/kg (Hartley and Kidd, 1987), 5,350 mg/kg (RTECS, 1985).
기존화학 물질 2013-3-5629
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P271 옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
P273 환경으로 배출하지 마시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
0
3 0

티디아주론 MSDS


5-Phenylcarbamoylamino-1,2,3-thiadiazole

티디아주론 C화학적 특성, 용도, 생산

화학적 성질

The pure product is a white odorless and tasteless crystalline solid. m.p.210~212.5°C (decomposition at 217°C), vapor pressure 4×10-9Pa) (25°C). Solubility at 25°C: dimethyl sulfoxide>500g/L, dimethylformamide>500g/L, cyclohexanone 21.5g/L, acetone 8g/L, methanol 4.5g/L, ethyl acetate 0.8 g/L, hexane 6mg/L, insoluble in aliphatic and aromatic hydrocarbons, solubility in water 31mg/L. The partition coefficient is 59 (pH=7.3). Stable below 200°C; stable to water at room temperature, half-life > 24d; half-life in soil < 60d.

용도

Thidiazuron is a non-purine containing urea derivative with cytokinin activity. Thidiazuron is used as a cotton defoliant and a plant growth regulator in tissue culture.

일반 설명

Thidiazuron is a systemic herbicide, widely employed as an effective plant growth regulator and pre-harvest defoliant for crops such as cotton.

농업용

Herbicide, Defoliant, Plant growth regulator: Used primarily as a cotton defoliant in order to increase the harvest yield. Not applied to food crops. Not approved for use in EU countries. Registered for use in the U.S. U.S. Maximum Allowable Residue Levels for Thidiazuron and its aniline-containing metabolites in or on the following food commodities: [40 CFR 180.403(a)]: cattle, fat 0.4 ppm; cattle, meat 0.4 ppm; cattle, meat byproducts 0.4 ppm; cotton, gin byproducts 24.0 ppm; cotton, undelinted seed 0.3 ppm; goat, fat 0.4 ppm; goat meat 0.4 ppm; goat, meat byproducts 0.4 ppm; hog, fat 0.4 ppm; hog, meat 0.4 ppm; hog, meat byproducts 0.4 ppm; horse, fat 0.4 ppm; horse, meat 0.4 ppm; horse, meat byproducts 0.4 ppm; milk 0.05 ppm; sheep, fat 0.4 ppm; sheep, meat 0.4 ppm; sheep, meat byproducts 0.4 ppm.

상품명

DAZE®; DEFOLIT®; DROPP®; GINSTAR EC® (thidiazuron + diuron); LEAFLESS® Tthidiazuron; SN 49537®

Safety Profile

Moderately toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of SOx and NOx.

환경귀착

Soil. The reported half-life in soil is approximately 26–144 days (Hartley and Kidd, 1987).
Photolytic. Rapidly converted to the photoisomer, 1-phenyl-3-(1,2,5-thiadiazol-3- yl)urea (Worthing and Hance, 1991). When thidiazuron adsorbed by soil was exposed to UV light (λ <290 nm), 1-phenyl-3-(1,2,5-thiadiazol-3-yl)urea formed as the majo

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