JP3155907B2 - Fresh flower freshener composition containing ethylene biosynthesis inhibitor - Google Patents

Fresh flower freshener composition containing ethylene biosynthesis inhibitor

Info

Publication number
JP3155907B2
JP3155907B2 JP15941395A JP15941395A JP3155907B2 JP 3155907 B2 JP3155907 B2 JP 3155907B2 JP 15941395 A JP15941395 A JP 15941395A JP 15941395 A JP15941395 A JP 15941395A JP 3155907 B2 JP3155907 B2 JP 3155907B2
Authority
JP
Japan
Prior art keywords
group
alkyl group
formula
atom
biosynthesis inhibitor
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP15941395A
Other languages
Japanese (ja)
Other versions
JPH0912402A (en
Inventor
直樹 御堂
道顕 岩田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Meiji Seika Kaisha Ltd
Original Assignee
Meiji Seika Kaisha Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Meiji Seika Kaisha Ltd filed Critical Meiji Seika Kaisha Ltd
Priority to JP15941395A priority Critical patent/JP3155907B2/en
Publication of JPH0912402A publication Critical patent/JPH0912402A/en
Application granted granted Critical
Publication of JP3155907B2 publication Critical patent/JP3155907B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、少なくとも2成分の混
合により相乗的に増強された作用を有する切り花の鮮度
保持剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cut flower freshness preserving composition having a synergistically enhanced action by mixing at least two components.

【0002】[0002]

【従来の技術】切り花の鮮度が低下する原因としては、
生け水中の茎の腐敗や導管の閉塞、栄養分の枯渇、内因
性のエチレンの増加などがあげらる。茎の腐敗や導管の
閉塞に対しては、8ーヒドロキシキノリンなどの殺菌剤や
水中汚物を沈澱させるための硫酸アルミニウム、水揚げ
を良くするための各種界面活性剤が用いられており、栄
養分の枯渇に対しては、ショ糖などの糖類が用いられて
いる。しかし、その効果には、ばらつきがあり明確では
ない。一方、内因性のエチレンの増加に対しては、1978
年にオランダのVeenらにより発見されたSTS(Ag(S2O3)2
3-)〔プランタ(Planta)140, 93〜96, 1978年〕がエ
チレンの作用を抑制し、カーネーション、宿根カスミソ
ウ等のエチレンが花の萎凋の主要因となる切り花に対し
ては明確な効果を示す。
2. Description of the Related Art The cause of a decrease in freshness of cut flowers is as follows.
Stem rot in the drinking water, clogged vessels, nutrient depletion, increased endogenous ethylene. For rot of stems and blockage of conduits, fungicides such as 8-hydroxyquinoline, aluminum sulfate for precipitating underwater contaminants, and various surfactants for improving landing are used to deplete nutrients. , Sugars such as sucrose are used. However, the effects vary and are not clear. On the other hand, for the increase of endogenous ethylene, 1978
STS (Ag (S 2 O 3 ) 2
3- ) [Planta 140 , 93-96, 1978] suppresses the action of ethylene, and has a clear effect on cut flowers in which ethylene such as carnation and gypsophila is the main cause of flower wilting. Show.

【0003】現在では、生産者は、多くの切り花に対し
てSTSを使用している。しかし、STSはその有効成分とし
て、重金属である銀を含んでいるため、環境汚染が懸念
されており、重金属を含まない安全な鮮度保持剤の実用
化が望まれている。
At present, producers use STS for many cut flowers. However, STS contains silver, which is a heavy metal, as an active ingredient, and therefore there is a concern about environmental pollution, and there is a demand for the practical use of a safe freshness-retaining agent containing no heavy metal.

【0004】一般式(I)The general formula (I)

【化2】 (I) 〔式中、R1は炭素原子数3〜4の直鎖状または分岐鎖
状の低級アルキル基を表すか、ハロゲン原子、C1-4
ルキル基、ヒドロキシル基、アルコキシル基、カルボキ
シル基、アルコキシカルボニル基、ニトロ基、アミノ基
またはベンジルオキシ基により置換されてもよいフェニ
ル基を表すか、あるいはピリジル基を表すか、もしくは
1はカルボキシル基またはアルコキシカルボニル基に
より置換されてもよいチエニル基を表し、R2およびR3
はそれぞれに水素原子、C1-4アルキル基、アルコキサ
リル基、アルコキシアルキル基、または式−C(=X)
−X−R4(ただし、Xは酸素原子または硫黄原子を、
4はC1-4アルキル基を表す)で示されるアルコキシカ
ルボニル基またはアルキルチオ−チオカルボニル基を表
すか、あるいはR2およびR3はR2とR3が結合している
窒素原子と共に共同して炭素数4〜5の複素環、例えば
モルホリノ基またはピペリジノ基を形成してもよく、も
しくはR2およびR3が結合している窒素原子と共に式−
N=CR5(R6)(ただし、R5とR6はそれぞれにC
1-4アルキル基を表す)の基を形成してもよい〕で示さ
れるスルホニルセミカルバジド誘導体またはその塩は、
本発明者らにより切り花の鮮度保持剤として有効である
ことが発見されている(WO 9505362)。一
方、アミノオキシ酢酸(AOAと略す)〔ホートサイエン
ス(Hortscience)15, 805〜806, 1980年〕、L-α-(2
-アミノエトキシビニル)グリシン(AVGと略す)〔ジャ
ーナル・オブ・ジ・アメリカン・ソサイアティ・フォー
・ホーティカルチュラル・サイエンス(Journal of the
American Society forHorticultural Science)102
517〜520, 1977年〕、2-アミノイソ酪酸(AIBと略す)
〔サイエンティア・ホーティカルチュレ(Scientia Hor
ticulturae)44,127〜134, 1990年〕も、エチレンの生
合成を阻害することにより、切り花の鮮度保持効果を示
すことが知られている。しかしながら、一般式(I)で
示されるスルホニルセミカルバジド誘導体とこれらのエ
チレン生合成阻害剤との混合時の効果については検討さ
れていなかった。
Embedded image (I) wherein R 1 represents a linear or branched lower alkyl group having 3 to 4 carbon atoms, or a halogen atom, a C 1-4 alkyl group, a hydroxyl group, an alkoxyl group, a carboxyl group Represents a phenyl group optionally substituted by an alkoxycarbonyl group, a nitro group, an amino group or a benzyloxy group, or represents a pyridyl group, or R 1 is a thienyl group optionally substituted by a carboxyl group or an alkoxycarbonyl group. R 2 and R 3
Is a hydrogen atom, a C 1-4 alkyl group, an alkoxalyl group, an alkoxyalkyl group, or a formula —C (= X), respectively.
—X—R 4 (where X is an oxygen atom or a sulfur atom,
R 4 represents a C 1-4 alkyl group), or an alkoxycarbonyl group or an alkylthio-thiocarbonyl group represented by the formula (I), or R 2 and R 3 are taken together with the nitrogen atom to which R 2 and R 3 are bonded. wherein Te heterocyclic ring 4-5 carbon atoms, for example may form a morpholino group or a piperidino group, or together with the nitrogen atom to which R 2 and R 3 are attached -
N = CR 5 (R 6 ) (where R 5 and R 6 are each C
Which represents a 1-4 alkyl group), or a sulfonyl semicarbazide derivative or a salt thereof,
The present inventors have found that it is effective as a preservative of freshness of cut flowers (WO 9505362). On the other hand, aminooxyacetic acid (abbreviated as AOA) [Hortscience 15 , 805-806, 1980], L-α- (2
-Aminoethoxyvinyl) glycine (abbreviated as AVG) [Journal of the American Society for Horticultural Science (Journal of the
American Society for Horticultural Science) 102 ,
517-520, 1977], 2-aminoisobutyric acid (abbreviated as AIB)
[Scientia Horticulture
ticulturae) 44 , 127-134, 1990] is also known to exhibit the effect of maintaining the freshness of cut flowers by inhibiting the biosynthesis of ethylene. However, the effect of mixing the sulfonyl semicarbazide derivative represented by the general formula (I) with these ethylene biosynthesis inhibitors has not been studied.

【0005】[0005]

【発明が解決しようとする課題】本発明の目的は、切り
花に対して優れた効果を有する鮮度保持剤を提供するこ
とにある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a freshness preserving agent having an excellent effect on cut flowers.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記の目
的を達成すべく鋭意検討した結果、一般式(I)で示さ
れるスルホニルセミカルバジド誘導体またはその塩と、
エチレンの生合成阻害剤またはその塩とを混合すること
により、それぞれの単独処理に比べて鮮度保持効果が相
乗的に増強されることを見出し本発明に至った。
Means for Solving the Problems As a result of intensive studies to achieve the above object, the present inventors have found that a sulfonyl semicarbazide derivative represented by the general formula (I) or a salt thereof,
The present inventors have found that the effect of preserving freshness is synergistically enhanced by mixing with a biosynthesis inhibitor of ethylene or a salt thereof, as compared with each of the individual treatments.

【0007】即ち本発明は、一般式(I)で示されるス
ルホニルセミカルバジド誘導体またはその塩と、エチレ
ンの生合成阻害剤またはその塩とを有効成分として含有
する切り花の鮮度保持剤組成物に関する。エチレン生合
成阻害剤としては、例えば、AOA、AVG、AIBなどが挙げ
られるが、特にこれらに限定されない。
That is, the present invention relates to a composition for preserving the freshness of cut flowers, comprising a sulfonylsemicarbazide derivative represented by the general formula (I) or a salt thereof and an ethylene biosynthesis inhibitor or a salt thereof as active ingredients. Examples of the ethylene biosynthesis inhibitor include, but are not particularly limited to, AOA, AVG, and AIB.

【0008】これらの有効成分は、各種濃度の水溶液と
して用いられ、その濃度は対象とする切り花の種類によ
り最適値が異なるため、特に限定されない。一般式
(I)で示されるスルホニルセミカルバジド誘導体また
はその塩は、その中でも好ましくは1,1−ジメチル−
4−(フェニルスルホニル)セミカルバジドは、1×10
-4〜0.1重量%の範囲で、エチレン生合成阻害剤又はそ
の塩、1×10-4〜1.0重量%の範囲で用いられる。組成
物中の混合割合としてはスルホニルセミカルバジド誘導
体:エチレン生合成阻害剤またはその塩=1:0.5〜
500、好ましくはスルホニルセミカルバジド誘導体:
エチレン生合成阻害剤またはその塩=1:10〜50
(但し、単位は重量%とする。)である。
[0008] These active ingredients are used as aqueous solutions of various concentrations, and the concentration is not particularly limited since the optimum value differs depending on the kind of cut flower to be treated. The sulfonyl semicarbazide derivative represented by the general formula (I) or a salt thereof is preferably 1,1-dimethyl-
4- (phenylsulfonyl) semicarbazide is 1 × 10
The ethylene biosynthesis inhibitor or a salt thereof is used in the range of 1 × 10 −4 to 1.0% by weight in the range of −4 to 0.1% by weight. Sulfonyl as mixing ratio of the composition semicarbazide derivatives: ethylene biosynthesis inhibitor or a salt thereof = 1: 0.5
500, preferably a sulfonyl semicarbazide derivative:
Ethylene biosynthesis inhibitor or a salt thereof = 1: 10 to 50
(However, the unit is% by weight.)

【0009】本発明の鮮度保持剤組成物の使用法として
は、前処理、後処理あるいは植物体への散布などがあげ
られる。前処理の方法としては、切り花の切り口を薬液
に、好ましくは1〜24時間浸せきすれば良い。後処理の
方法としては、切り花を薬液の入った花瓶などに生けて
おけば良い。散布処理の方法としては、スプレーなど
で、切り花全体に薬液を散布すれば良い。
The method for using the freshness-preserving composition of the present invention includes pretreatment, post-treatment, and application to plants. As a pretreatment method, the cut end of the cut flower may be immersed in a chemical solution, preferably for 1 to 24 hours. As a post-treatment method, cut flowers may be placed in a vase or the like containing a chemical solution. As a spraying method, a chemical solution may be sprayed on the entire cut flower by spraying or the like.

【0010】本発明の鮮度保持剤組成物は、添加剤(殺
菌剤、界面活性剤など)や、市販されている他の鮮度保
持剤と混合して用いても良く、本発明品を用いた後に添
加剤や市販されている他の鮮度保持剤を用いても良い。
The freshness-maintaining composition of the present invention may be used as a mixture with additives (bactericides, surfactants, etc.) or other commercially available freshness-maintaining agents. An additive or another commercially available freshness-preserving agent may be used later.

【0011】本発明の鮮度保持剤を適用できる花として
は、カーネーション、デルフィニウム、スイートピー、
宿根カスミソウ、ユリ、フリージア、チューリップ、洋
ラン等の切り花、あるいは鉢物などがあげられる。
The flowers to which the freshness preserving agent of the present invention can be applied include carnation, delphinium, sweet pea,
Examples include cut flowers such as syrup, gypsophila, lily, freesia, tulip, and orchid, and potted plants.

【0012】[0012]

【実施例】【Example】

試験例1 カーネーション切り花の鮮度保持効果 神奈川県秦野市の農家において栽培されたカーネーショ
ン(品種;フランシスコ)を10 cmの長さに切り、50 ml
の薬液の入った管ビン(φ3×12 cm)に、切り花を1本
ずつ入れ、その後25℃の恒温室にて切り花の状態を観察
した。各試験区とも10反復とした。結果を表1に示
す。花の萎凋が見られるまでの日数を花持ち日数として
表し、さらに対照区と比較したときの花持ち延長日数と
それぞれ単独処理の花持ち延長日数を相加した日数も併
せて示した。また、花持ち延長日数および相加日数は以
下のように定義する。 花持ち延長日数=各処理群の花持ち日数−対照区の花持
ち日数 相加日数=各濃度のスルホニルセミカルバジド誘導体処
理群の花持ち延長日数+各エチレン生合成阻害剤処理群
の花持ち延長日数
Test Example 1 Freshness preservation effect of cut carnation flower Carnation (cultivar: Francisco) cultivated at a farmhouse in Hadano City, Kanagawa Prefecture, was cut into 10 cm lengths and 50 ml
The cut flowers were placed one by one into a tube bottle (φ3 × 12 cm) containing the liquid medicine, and then the state of the cut flowers was observed in a constant temperature room at 25 ° C. Each test group had 10 replicates. Table 1 shows the results. The number of days until flower wilting was observed was expressed as the number of days of flowering, and the number of days of extended flowering when compared with the control plot and the number of days when the number of days of flowering extended alone were added were also shown. The extension days and the addition days of the flower life are defined as follows. Extended days of flowering = Days of flowering in each treatment group-Days of flowering in control group Addition days = Extended days of flowering in groups treated with sulfonylsemicarbazide derivative at each concentration + Extended days of flowering in groups treated with each ethylene biosynthesis inhibitor

【0013】 表1 処理 花持ち日数 花持ち延長 相加 (日) 日数(日) 日数(日) 対照区 7.8 − − 1 ppm 1,1-ジメチル-4-(フェニル 9.4 1.6 − スルホニル)セミカルバジド 10 ppm AOA 8.2 0.4 − 10 ppm AVG 8.6 0.8 − 50 ppm AIB 7.9 0.1 − 1 ppm 1,1-ジメチル-4-(フェニル 11.5 3.7 2.0 スルホニル)セミカルバジド + 10 ppm AOA 1 ppm 1,1-ジメチル-4-(フェニル 11.7 3.9 2.4 スルホニル)セミカルバジド + 10 ppm AVG 1 ppm 1,1-ジメチル-4-(フェニル 11.4 3.6 1.7 スルホニル)セミカルバジド + 50 ppm AIB Table 1 Treatment Number of days with flower extension Extended with flower life Addition (days) Days (days) Days (days) Control group 7.8--1 ppm 1,1-dimethyl-4- (phenyl 9.4 1.6-sulfonyl) semicarbazide 10 ppm AOA 8.2 0.4-10 ppm AVG 8.6 0.8-50 ppm AIB 7.9 0.1-1 ppm 1,1-dimethyl-4 -(Phenyl 11.5 3.7 2.0 sulfonyl) semicarbazide +10 ppm AOA 1 ppm 1,1-dimethyl-4- (phenyl 11.7 3.9 2.4 Sulfonyl) semicarbazide +10 ppm AVG 1 ppm 1,1-dimethyl-4- (phenyl 11.4 3.6 1.7 Sulfonyl) semicarbazide + 50 ppm AIB

【0014】表1から明らかなように、1,1-ジメチル-4
-(フェニルスルホニル)セミカルバジドとAOA、または
1,1-ジメチル-4-(フェニルスルホニル)セミカルバジ
ドとAVG、または1,1-ジメチル-4-(フェニルスルホニ
ル)セミカルバジドとAIBとを混合したときの効果は、
それぞれの単独使用の花持ち延長日数の相加以上の効果
を示した。
As is clear from Table 1, 1,1-dimethyl-4
-(Phenylsulfonyl) semicarbazide and AOA, or
The effect of mixing 1,1-dimethyl-4- (phenylsulfonyl) semicarbazide and AVG or 1,1-dimethyl-4- (phenylsulfonyl) semicarbazide and AIB is as follows:
Each single use showed an effect that was greater than or equal to the extension of the flower life extension days.

【0015】[0015]

【発明の効果】本発明によれば、切り花の鮮度を良好な
状態で長期に保つ鮮度保持剤を提供することができる。
According to the present invention, it is possible to provide a freshness preserving agent which maintains the freshness of cut flowers in a good state for a long period of time.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平9−12401(JP,A) 特開 平5−229902(JP,A) 特開 平4−49203(JP,A) 特開 平3−93701(JP,A) 特開 昭62−249962(JP,A) 特開 平5−17426(JP,A) 特開 平5−268873(JP,A) 特開 平6−279203(JP,A) 特開 平7−48203(JP,A) 特表 平7−500250(JP,A) 国際公開95/5362(WO,A1) (58)調査した分野(Int.Cl.7,DB名) A01N 3/02 JICSTファイル(JOIS) CA(STN) REGISTRY(STN)──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-9-12401 (JP, A) JP-A-5-229902 (JP, A) JP-A-4-49203 (JP, A) JP-A-3- 93701 (JP, A) JP-A-62-249962 (JP, A) JP-A-5-17426 (JP, A) JP-A-5-268873 (JP, A) JP-A-6-279203 (JP, A) JP-A-7-48203 (JP, A) JP-A-7-500250 (JP, A) International publication 95/5362 (WO, A1) (58) Fields investigated (Int. Cl. 7 , DB name) A01N 3 / 02 JICST file (JOIS) CA (STN) REGISTRY (STN)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】一般式(I) 【化1】 (I) 〔式中、R1 は炭素原子数3 〜4 の直鎖状または分岐
鎖状の低級アルキル基を表すか、ハロゲン原子、C1- 4
アルキル基、ヒドロキシル基、アルコキシル基、カル
ボキシル基、アルコキシカルボニル基、ニトロ基、アミ
ノ基またはベンジルオキシ基により置換されてもよいフ
ェニル基を表すか、あるいはピリジル基を表すか、もし
くはR1 はカルボキシル基またはアルコキシカルボニル
基により置換されてもよいチエニル基を表し、R2 およ
びR3はそれぞれに水素原子、C1-4 アルキル基、アル
コキサリル基、アルコキシアルキル基、または式−C
(=X)−X −R4 (ただし、X は酸素原子または硫
黄原子を、R4はC1- 4 アルキル基を表す)で示される
アルコキシカルボニル基またはアルキルチオ−チオカル
ボニル基を表すか、あるいはR2 およびR3 はR2 とR
3 が結合している窒素原子と共に共同して炭素数4 〜
5 の複素環、例えばモルホリノ基またはピペリジノ基
を形成してもよく、もしくはR2 およびR3 が結合して
いる窒素原子と共に式−N=CR5(R6 )(ただし、
5 とR6 はそれぞれにC1-4 アルキル基を表す)の基
を形成してもよい〕で示されるスルホニルセミカルバジ
ド誘導体またはその塩と、アミノオキシ酢酸、L−α−
(2−アミノエトキシビニル)グリシンおよび2−アミ
ノイソ酪酸の中から選択される少なくとも1種のエチレ
ン生合成阻害剤とを有効成分とする切り花の鮮度保持剤
組成物。
1. A compound of the general formula (I) (I) [In the formula, R 1 represents a linear or branched lower alkyl group having 3 to 4 carbon atoms, or a halogen atom, C 1-4
An alkyl group, a hydroxyl group, an alkoxyl group, a carboxyl group, an alkoxycarbonyl group, a nitro group, an amino group or a phenyl group which may be substituted by a benzyloxy group, a pyridyl group, or R 1 is a carboxyl group Or a thienyl group which may be substituted by an alkoxycarbonyl group, wherein R 2 and R 3 are each a hydrogen atom, a C 1-4 alkyl group, an alkoxalyl group, an alkoxyalkyl group, or a compound of the formula —C
(= X) -X -R 4 (where the X represents an oxygen atom or a sulfur atom, R 4 represents a C 1-4 alkyl group) alkoxycarbonyl group or an alkylthio represented by - represent a thiocarbonyl group, or R 2 and R 3 are R 2 and R
3 together with the nitrogen atom to which it is attached
5 may form a heterocycle, such as a morpholino or piperidino group, or together with the nitrogen atom to which R 2 and R 3 are attached, the formula —N = CR 5 (R 6 )
R 5 and R 6 each independently represent a C 1-4 alkyl group), or a salt thereof, aminooxyacetic acid, L-α-
(2-aminoethoxyvinyl) glycine and 2-amino
A fresh flower preservative composition comprising, as an active ingredient, at least one ethylene biosynthesis inhibitor selected from noisobutyric acid .
【請求項2】スルホニルセミカルバジド誘導体が1 ,
1−ジメチルー4 −(フェニルスルホニル)セミカル
バジドである請求項1記載の切り花の鮮度保持剤組成
物。
2. The method according to claim 1, wherein the sulfonyl semicarbazide derivative is 1, 2 or 3.
The composition for retaining freshness of cut flowers according to claim 1, which is 1-dimethyl-4- (phenylsulfonyl) semicarbazide.
JP15941395A 1995-06-26 1995-06-26 Fresh flower freshener composition containing ethylene biosynthesis inhibitor Expired - Fee Related JP3155907B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15941395A JP3155907B2 (en) 1995-06-26 1995-06-26 Fresh flower freshener composition containing ethylene biosynthesis inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15941395A JP3155907B2 (en) 1995-06-26 1995-06-26 Fresh flower freshener composition containing ethylene biosynthesis inhibitor

Publications (2)

Publication Number Publication Date
JPH0912402A JPH0912402A (en) 1997-01-14
JP3155907B2 true JP3155907B2 (en) 2001-04-16

Family

ID=15693214

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15941395A Expired - Fee Related JP3155907B2 (en) 1995-06-26 1995-06-26 Fresh flower freshener composition containing ethylene biosynthesis inhibitor

Country Status (1)

Country Link
JP (1) JP3155907B2 (en)

Also Published As

Publication number Publication date
JPH0912402A (en) 1997-01-14

Similar Documents

Publication Publication Date Title
JP2002510602A (en) Peroxyacid treatment to control pathogenic organisms on growing plants
JP2001521878A (en) Pesticides against phytopathogenic microorganisms
JP3155907B2 (en) Fresh flower freshener composition containing ethylene biosynthesis inhibitor
JP3201038B2 (en) Freshener for cut flowers and leafy vegetables
JP3155906B2 (en) Composition for maintaining freshness of cut flowers containing a reducing agent
JPS5828244B2 (en) Plant growth inhibitor composition
JPS632904A (en) Plant growth regulator
JP2673535B2 (en) Plant growth promotion method
JP3047599B2 (en) Composition for maintaining freshness of cut flowers
JP3764195B2 (en) Freshness retaining composition for cut flowers containing gibberellin
EP1886563B1 (en) High-strength, low-temperature stable herbicidal formulations of 2,4-Dichlorophenoxy acetic acid salts
EP0714889B1 (en) Sulfonylsemicarbazide derivative and composition for keeping cut flower freshness
JP3793594B2 (en) Freshness retaining composition for cut flowers containing cytokinin
JP2999527B2 (en) Freshener and method for maintaining freshness of cut flowers
JP3096158B2 (en) Freshener and method for maintaining freshness of cut flowers
JPH04360802A (en) Agent for keeping freshness of cut flower and freshness-keeping method
JP2965854B2 (en) Plant freshness preservative
JPH06145002A (en) Agent for preserving freshness of cut flower and method for preserving freshness
JPH0881301A (en) Agent for keeping freshness of cut flower
JPH1081601A (en) Freshness retaining agent for cut flower
EP0010736A1 (en) Fungicidal compositions for apple canker and powdery mildews
KR810000898B1 (en) Compositions of plant growth regulator
JPH05155716A (en) Plant growth activator
CA2555915C (en) High-strength, low-temperature stable herbicidal formulations of 2,4-dichlorophenoxy acetic acid salts
JP2001151601A (en) Freshness retaining agent and method for retaining freshness

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080202

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090202

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100202

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110202

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110202

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120202

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120202

Year of fee payment: 11

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120202

Year of fee payment: 11

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130202

Year of fee payment: 12

LAPS Cancellation because of no payment of annual fees