이마자필

그림문자(GHS)

• 그림문자(GHS)

  

• 신호 어

  Warning

• 유해·위험 문구

  H319：눈에 심한 자극을 일으킴

• 예방조치문구

  P264：취급 후에는 손을 철저히 씻으시오.

  P264：취급 후에는 손을 철저히 씻으시오.

  P280：보호장갑/보호의/보안경/안면보호구를 착용하시오.

  P305+P351+P338：눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

  P337+P313：눈에 대한 자극이 지속되면 의학적인 조치· 조언를 구하시오.

이마자필 MSDS

• Imazapyr

이마자필 화학적 특성, 용도, 생산

• 화학적 성질

  solid

• 용도

  Imazapyr is an analytical standard used for proteomics research.

• Pharmacology

  Imazapyr kills plants by inhibiting acetolactate synthase (ALS) (I50 = 5 μM), which is the first common enzyme in the biosynthesis of the branched chain amino acids, valine, leucine, and isoleucine. Imazapyr is rapidly absorbed through the leaves of plants. Once it enters the plant, imazapyr rapidly translocates to the growing points and growth ceases within 1 day after herbicide application followed by chlorosis and then necrosis of the growing points. Total plant death will occur within 2 to 3 weeks after treatment.

• 환경귀착

  Imazapyr is weakly to moderately adsorbed on sandy loam and silt loam soils. The Freundlich adsorption coefficient ranges from 0 to 7.8 (15). Because imazapyr is a weak acid and exists in different ionic states, soil pH has an effect on soil binding properties. The anionic form predominates at soil pH as low as 5.5, and this form bindsweakly to soil. The neutral or molecular form is important at soil pH from 4 to 6.5. This form binds to soil organic matter and clay. The cationic form is important at pH less than 4. Because the soil is a heterogeneous mixture of acid and base chemical groups, there may be sites within a particular soil that are 2 to 3 pH units higher or lower than the average pH. The cationic form will bind tightly to the lower pH components. Because of these interactions, small decreases in pH below 6 will result in large increases in binding. The half-life of imazapyr in the soil is 25–142 d (14). Imazapyr remains in the top 30 cm of the soil with low leaching potential. The degradation route of imazapyr in the soil has not been determined.

• 신진 대사

  Plant Metabolism. The selectivity of imazapyr is due to differential rates and routes of metabolism in tolerant crops versus susceptible weeds (3). The half-life of imazapyr in tolerant crops has not been accurately determined. The metabolic route of imazapyr is not clear. The parent compound can be metabolized to a tricyclic compound (33, Fig. 15) in some species, but the primary metabolite is an imidazopyrrolo-pyridine derivative (34, Fig. 15). This compound does not inhibit acetolactate synthase, the target site for the imidazolinones, and it is immobile in the plant (4).
  Animal Metabolism. Metabolism studies in the rat showed that imazapyr is rapidly excreted in the urine (5). There was no accumulation of imazapyr or any of its derivatives in the liver, kidney, muscle, fat, or blood.

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