JPS58213714A - Preparation of tablet - Google Patents
Preparation of tabletInfo
- Publication number
- JPS58213714A JPS58213714A JP9709582A JP9709582A JPS58213714A JP S58213714 A JPS58213714 A JP S58213714A JP 9709582 A JP9709582 A JP 9709582A JP 9709582 A JP9709582 A JP 9709582A JP S58213714 A JPS58213714 A JP S58213714A
- Authority
- JP
- Japan
- Prior art keywords
- sodium
- tablet
- tablets
- acid
- binder
- 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.)
- Granted
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Medicinal Preparation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は錠剤の製造法に関する。赫に錠剤表面に一凹凸
を生じない打錠成型による錠剤の製造法に関する。
′
錠剤は一般VCは粉末或は顆粒状の原料の−成分或は多
成分混合系を打錠して作られる。この際、粉末或it顆
粒成分をそのまま打錠しても錠剤を得ることは出来るが
、錠剤の硬度、作業能率を向上させる為には、一般に結
合剤が添加される。結合剤としては一般的には水が使用
されるが、水を添加したくない場合或は水によル分解を
受ける様な成分が添加されている場合には水を結合剤と
して用いることは好ましくない。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing tablets. This invention relates to a method for manufacturing tablets by compression molding that does not cause any unevenness on the tablet surface.
' Tablets are generally made by compressing powdered or granular raw materials or multi-component mixtures. At this time, although tablets can be obtained by compressing the powder or granule components as they are, a binder is generally added to improve the hardness and working efficiency of the tablets. Water is generally used as a binder, but if you do not want to add water or if components that are likely to be decomposed by water are added, water cannot be used as a binder. Undesirable.
この場合には非水系の結合剤として40U以上の融点を
示す有機化合物の粉末を添加して打錠される。この様に
して打錠する際の問題点としてはチッピング(表面に凹
凸が生じ、表面の外観が低下する現象)がある。In this case, a powder of an organic compound having a melting point of 40 U or more is added as a non-aqueous binder and the tablets are compressed. A problem with tabletting in this manner is chipping (a phenomenon in which irregularities occur on the surface and the appearance of the surface deteriorates).
従来かかるチッピングを防止する対策としてはステアリ
ン酸カルシウム、ステアリン酸、メルク等を添加するこ
とが行なわれているが、これらは錠剤を水に溶かして使
用する場合、水に不溶の為、水面に浮上し、不快感を与
えるため好ましくない。Conventional measures to prevent such chipping have been to add calcium stearate, stearic acid, Merck, etc., but when tablets are dissolved in water and used, these are insoluble in water and float to the surface of the water. , which is undesirable because it causes discomfort.
本発明者らはチッピングを生じない打錠方法を検討し九
結果、結合剤として用いる融点4゜C以上を示す有機化
合物と、打錠成型さるべき無機又は有機化合物成分の少
なくとも一部とをあらかじめその結合剤の融点より高い
温度で加熱、溶融混合後、冷却、粉末化することにょシ
チツピングを起さず打錠することが出来ることを見い出
して本発明に到ったものである。The present inventors investigated a tableting method that does not cause chipping, and found that an organic compound with a melting point of 4°C or higher to be used as a binder and at least a part of the inorganic or organic compound components to be formed into tablets were mixed in advance. The present invention was achieved by discovering that tableting can be achieved without causing chipping by heating, melting and mixing at a temperature higher than the melting point of the binder, then cooling and pulverizing.
即ち本発明は実質的に水分を含まないか或はsor以下
で結晶水を遊離しない、無機或は有機化合物を打錠成型
するに際して、上記打錠成型さるべき成分の全部或は少
なくとも一部を融A4or以上を示す結合剤成分とあら
かじめ結合剤成分の融点以上のm度で加熱、溶融混合後
、冷却、粉末化し、これに必要に応じ他の成分を添加混
合して打錠成型することを特徴とする錠剤の製造方法に
係わるものである。That is, in the present invention, when tabletting an inorganic or organic compound that does not substantially contain water or does not release water of crystallization at less than sor, all or at least a portion of the ingredients to be tableted are After heating and melt-mixing the binder component exhibiting a melting point of A4or or higher at m degrees above the melting point of the binder component, the mixture is cooled and powdered, and other components are added and mixed as necessary to form a tablet. The present invention relates to a method for producing a characteristic tablet.
本発明の方法で打錠する成分は実質的に水を含まないか
或は結晶水として水が含まれる場合にはSaC以下、好
ましくtj:100−C以下では結晶水が遊離しない物
質である。これらの物質としては硫酸ナトリウム、炭酸
ナトリウム、重炭酸ナトリウム、ピロリン酸ナトリウム
、トリポリリン酸ナトリウム、第1リン酸ナトリウム、
第2リン酸ナトリウム等のナトリクム塩、或はそれらの
カリウム塩、カルシウム塩、マグネシウム塩の如き無機
塩、過炭酸す) IJウム、過硼酸ナトリウム、モノ過
硫酸カリ複塩(例えばに2So、 : KH8O,:
KH8O1lのモル比が1:2:1の複塩)、4 Ha
280. ’ 2 H2O2・Na0tの如き硫酸ナト
リウム−塩化す) +7ウム一過酸化水素付加体等の酸
素系泳白剤、ジクロルイソシアヌール酸、及びそのアル
カリ金属塩もしくはアルカリ土類金属塩、トリクロルイ
ソシアヌール酸、ジクロルジメチルヒダントイン、テト
ラクロルグリコールウリル、次亜塩素酸カルシウム、次
亜塩素酸リチウム尋の水溶液中で次亜塩1g酸又は次亜
、塩素塩を生成する有機或は無機塩素化合物、修酸、酒
石酸、クエン酸、コノ1り酸、グルコン酸、アジピン酸
の如き有機酸或はそのアルカリ金属塩もしくはアルカリ
土類金属塩等であシ、更に必要により殺菌剤、染料、顔
料等も使用出来る。The ingredient to be tableted by the method of the present invention is a substance that does not substantially contain water, or if water is contained as water of crystallization, water of crystallization is not liberated at temperatures below SaC, preferably below tj: 100-C. These substances include sodium sulfate, sodium carbonate, sodium bicarbonate, sodium pyrophosphate, sodium tripolyphosphate, sodium monophosphate,
Sodium salts such as dibasic sodium phosphate, or their inorganic salts such as potassium salts, calcium salts, and magnesium salts, percarbonate, sodium perborate, potassium monopersulfate double salts (for example, 2So, KH8O,:
double salt with a molar ratio of KH8O1l of 1:2:1), 4 Ha
280. ' 2 Sodium sulfate-chloride such as H2O2.Na0t) +7um Oxygen-based dyes such as monohydrogen peroxide adducts, dichloroisocyanuric acid and its alkali metal salts or alkaline earth metal salts, trichloroisocyanuric acid acid, dichlorodimethylhydantoin, tetrachloroglycoluril, calcium hypochlorite, lithium hypochlorite in an aqueous solution of 1 g of hypochlorite acid or hypochlorite, an organic or inorganic chlorine compound that produces a chlorine salt; Acids, organic acids such as tartaric acid, citric acid, conolinic acid, gluconic acid, adipic acid, or their alkali metal salts or alkaline earth metal salts, etc., and if necessary, fungicides, dyes, pigments, etc. are also used. I can do it.
これらの物質は実質的には無水であることが望ましいが
、例えば結晶水を含んだ炭酸す) IJウム・1水和物
、ピロリン酸ナトリウム・10水和物、トリポリリン酸
ナトリウム・6水和物、NaBO3・4H20で示され
る過硼酸ナトリウム等も使用することが出来る。It is desirable that these substances be substantially anhydrous, but for example, carbonate containing water of crystallization, IJum monohydrate, sodium pyrophosphate decahydrate, sodium tripolyphosphate hexahydrate, etc. , NaBO3.4H20, etc. can also be used.
結合剤として用いる40tl’以上の融点を示す物質と
して好ましいものはエチレンオキサイド付加物であり、
例えけポリエチレングリコール(分子量2000〜20
000 )、ポリオキシエチレン(付加モル数n=1
5以上)アルキル(Oa〜C22)エーテルがあげられ
る。その他ポリオキシエチレン(n=15以上)脂肪酸
(0□2〜C22)エステル、及び脂肪酸(Cユ2〜0
22)等も使用出来る。これら結合剤の添加11は打錠
する混合物全体の0.1〜1o M、*tibが2i!
I尚であり、好ましくは0.5〜5重量−である。A preferable substance having a melting point of 40 tl' or more used as a binder is an ethylene oxide adduct;
For example, polyethylene glycol (molecular weight 2000-20
000), polyoxyethylene (number of added moles n=1
5 or more) alkyl (Oa to C22) ethers. Other polyoxyethylene (n=15 or more) fatty acid (0□2~C22) ester, and fatty acid (C2~0
22) etc. can also be used. The addition of these binders 11 is from 0.1 to 1o M of the entire mixture to be tableted, *tib is 2i!
I, preferably 0.5 to 5% by weight.
これらの結合剤と共にあらかじめ加熱、溶融処理される
成分は打錠成製さるべき成分の全部であってもよく、又
その一部を処理してもよい。The ingredients to be heated and melted in advance together with these binders may be all of the ingredients to be made into tablets, or only a portion thereof may be treated.
錠剤中に反応性に富む物質、或は熱安定性の低い物質を
配合する場合には、他の不活性な成分、例えば重炭酸ナ
トリウム、硫酸ナトリウムの様な物質と結合剤とを加熱
溶融、混合処理後、冷却粉末化した系に後から添加混合
して打錠するのがよい。When a highly reactive substance or a substance with low thermal stability is incorporated into a tablet, other inert ingredients such as sodium bicarbonate or sodium sulfate and a binder may be melted by heating. After the mixing treatment, it is preferable to add the mixture to the cooled powdered system and then tablet.
本発明の方法によシ打錠して得られた錠剤は、その成分
組成に応じ洗剤、標白剤、プール用殺菌剤、浴剤、風呂
水清浄剤その他の用途に利用出来るが、何れも表面に凹
凸のない外観のすぐれたものが得られる。The tablets obtained by compressing the tablets according to the method of the present invention can be used for detergents, whitening agents, pool disinfectants, bath additives, bath water cleaners, and other uses, depending on the composition of the tablets. A product with an excellent appearance without any unevenness on the surface can be obtained.
以下本発明の実施例を示すが、本発明はこれらの実施例
に限定されるものではない。尚配合割合はm′J1mを
示す。Examples of the present invention will be shown below, but the present invention is not limited to these Examples. The blending ratio is m'J1m.
実施例1
配合A、Bについては原料粉末をそのまま混合した。配
合Cについては混合系をあらかじめ卓上ニーダ−(入江
商会: PNV−1型)を用いて65Cで20分間加熱
溶溶融金後、冷却した。Example 1 For formulations A and B, the raw material powders were mixed as they were. For Formulation C, the mixed system was heated in advance at 65C for 20 minutes using a table kneader (Irie Shokai: Model PNV-1) and then cooled.
冷却しただけで混合系は粉末状を呈し、粉砕、篩分けを
要しなかった。The mixed system took on a powder form just by cooling, and no pulverization or sieving was required.
これらA、 B、 Oの粉末を夫々打錠機(畑鉄工
所: HT−8・1型)でS 17錠になる様に打錠し
た。Aは10錠打錠後すでに、杆・白への粉末付着が生
じ、錠剤の表面に凹凸が生じていた。These A, B, and O powders were each compressed into 17 S tablets using a tablet machine (Hata Tekkosho: Model HT-8/1). After 10 tablets of A were compressed, powder adhesion to the rods and whites had already occurred, and unevenness had formed on the surface of the tablets.
又Bは錠剤#g1度が弱く、軽く指で押えるだけで錠剤
が崩壊した。本屋式硬度計で測定した結果は5〜61Q
/錠の範凹であった。こtに対して0a100錠打錠し
た時点でも杆・白への付着はなく、錠剤の表面は伺ら変
化がなかった。又硬度も15〜23−で十分な′f&度
を示した。In addition, tablet #g1 of B was weak, and the tablet disintegrated when pressed lightly with a finger. The result measured with a bookstore type hardness tester is 5-61Q.
/ It was a lock. Even when 100 tablets of 0a were compressed, there was no adhesion to the rod or white, and there was no change in the surface of the tablets. Further, the hardness was 15 to 23-, showing a sufficient hardness.
以上よp本発明による打錠方法が打錠性を改良するだけ
でなく、結合剤の添加量も少なくてよく、経済的である
ことがわかる。From the above, it can be seen that the tableting method according to the present invention not only improves tableting properties, but also requires less amount of binder, making it economical.
上記の如く作られた配合0の過炭酸ナトリウムの錠剤は
標日剤として洗瘤時に3〜4錠添加し洗剤の補助剤とし
て使用出来る。The sodium percarbonate tablets of formulation 0 prepared as described above can be added as a date marking agent and used as an adjunct to detergents by adding 3 to 4 tablets at the time of washing the tumor.
実施例2
ジクロルイソシアヌール酸カリ 30酒 石
酸 30重炭酸ナト
リウム 38.5ポリエチレングリコール(
分子z40oO) 1.5上記上合中重度酸ナトリ
ウムとポリエチレングリコール4000の混合系を実施
例の配合0の場合と同様に卓上ニーター−で10分間混
合・溶融、冷却1〜た。処理品は当初の粉末とほとんど
同様の状態であった。これに酒石酸、ジクロルイソシア
ヌール酸カリを混合し、実施例1と同様に打錠した。1
00錠打錠しても杆・白への粉末付着はなく、錠剤表面
rc凹凸は生じなかった。Example 2 Potassium dichloroisocyanurate 30 Tartaric acid 30 Sodium bicarbonate 38.5 Polyethylene glycol (
Molecule z40oO) 1.5 The mixed system of sodium heavy acid and polyethylene glycol 4000 in the above reaction was mixed and melted in a table kneader for 10 minutes, and cooled for 1 to 10 minutes, as in the case of formulation 0 in the example. The treated product was in almost the same condition as the original powder. This was mixed with tartaric acid and potassium dichloroisocyanurate, and tableted in the same manner as in Example 1. 1
Even after 00 tablets were compressed, there was no powder adhesion to the rods or whites, and no rc unevenness occurred on the tablet surface.
本錠剤は家庭で入浴仮、1錠添加しておくと、細−の繁
殖を防止して、2回たて返しても風呂水のにごシ、ヌル
ヌル、においの発生を防止出来る。If you add one tablet of this tablet to your bath at home, it will prevent the growth of fine particles and prevent the bath water from becoming cloudy, slimy, and smelly even after you turn it over twice.
実施例3
ジクロルイソシアヌール酸ナトリウム 50トリポ
リリン酸ナトリウム 48ミリスチン
酸 2上記処方中トリポリリン
酸ナト1Jウム粉末とミ’)スチン*fyocで10分
間加熱溶溶融金し、冷却、粉末化した。これにジクロル
インシアヌール酸ナトリウムを添加して突施991と同
様にして5t/錠の錠剤に打錠した所、100錠打錠し
ても杆・臼への粉末付着はなく、錠斉]表面に凹凸は生
じなかった。Example 3 Sodium dichloroisocyanurate 50 Sodium tripolyphosphate 48 Myristic acid 2 Sodium tripolyphosphate in the above formulation 1 Jum powder and 1) Stin*fyoc were heated and melted for 10 minutes, cooled and powdered. When sodium dichloroincyanurate was added to this and the tablets were compressed into 5 tons/tablet in the same manner as Tushu 991, there was no powder adhesion to the rod or die even after 100 tablets were compressed. No unevenness occurred on the surface.
本市は欅白剤とL2て用いることt1来る。Motoichi will use Keyaki whitening agent and L2.
出願人代理人 古 谷 馨
手続補正書(自発)
昭和57年7月21日
特軒庁長官 若 杉 和 夫 殿
1、事件の表示
特願昭17−97095号
2、発明の名称
錠剤の製造方法
3、 補正をする者
事件との関係 特許出願人
(091)花王石鹸株式会社
4代理人
東京都中央区日本橋横山町1の75中井ビル明細書の発
明の詳細な説明の欄
6、 補正の内容
88−Applicant's agent Kaoru Furuya Procedural amendment (spontaneous) July 21, 1980 Director-General of the Tokuken Agency Kazuo Wakasugi 1, Indication of the case Patent application No. 17-97095 2, Name of the invention Method for manufacturing tablets 3. Relationship with the case of the person making the amendment Patent applicant (091) Kao Soap Co., Ltd. 4 Agent 75 Nakai Building, 1-1 Nihonbashi Yokoyama-cho, Chuo-ku, Tokyo Column 6 of the detailed description of the invention in the specification, Contents of the amendment 88-
Claims (1)
を遊離しない、無機或は有機化合物を打錠IR型するに
際して、上記打錠ji!型さるべき成分の全部或は少な
くとも一部を111440tl’以上を示す結合剤成分
乏あらかじめ結合剤成分の融点以上の温度で加熱、溶融
混合後、冷却、粉末化し、これに必要に応じ他の成分を
添加混合して打錠成型すゐことを特徴とする錠剤の製造
方法。 2 打錠成型さるべき成分が1炭酸す)IJウム。 過訣酸ナトリウム、itsナトリウム、炭酸ナトリウム
、ジクロルイソシアヌール酸、ジクロルイソシアヌール
酸ナトリウム及びジクロルイソシアヌール酸カリウムか
らなる群から辿けれる一種又は二種以上であ如、結合剤
成分がポリエチレングリコール(分子ii 2000〜
20000)又はポリエチレングリコールアルキルエー
テル(エチレンオキサイド付加モル数15以上、アルキ
ルの炭票数8〜22)及び脂肪酸からなる群から選ばれ
る一種又は二種以上である特許請求の範il!′第1項
記載の錠剤の製造方法。 6 重炭酸ナトリウムと分子量2000〜tooo。 のポリエチレングリコールとを60〜100Cで加熱溶
融混合後、冷却、□粉末化し、これに酒石酸、修酸、ク
エン酸及びコノ・りIlの中から選ばれる一種もしくは
二種以上の混合物、或は(及び)ジクロルイソシアヌー
ル酸ナトリウム、ジクロルイソシアヌール酸カリウム又
はそれらの混合物を添加して打錠成型する特許請求の範
囲第2項記載の錠剤の製造方法。[Claims] 1. When compressing into an IR tablet an inorganic or organic compound that does not substantially contain water or does not release water of crystallization at hsoc or lower, the above-mentioned ji! All or at least some of the components to be molded are heated at a temperature higher than the melting point of the binder component, melt-mixed, and then cooled and powdered, followed by adding other components as necessary. 1. A method for producing tablets, which comprises adding and mixing and compressing into tablets. 2. Ingredients to be formed into tablets are 1 carbonate) IJum. The binder component may be one or more selected from the group consisting of sodium peroxide, sodium nitrate, sodium carbonate, dichloroisocyanuric acid, sodium dichloroisocyanurate, and potassium dichloroisocyanurate. Polyethylene glycol (molecule II 2000~
20,000) or polyethylene glycol alkyl ether (the number of moles of ethylene oxide added is 15 or more, the number of alkyl carbons is 8 to 22), and one or more kinds selected from the group consisting of fatty acids! 'A method for producing a tablet according to item 1. 6 Sodium bicarbonate and molecular weight 2000~toooo. After melting and mixing with polyethylene glycol by heating at 60 to 100 C, cooling and □ powdering, to this is added a mixture of one or more selected from tartaric acid, oxalic acid, citric acid and condensate, or ( and) the method for producing a tablet according to claim 2, which comprises adding sodium dichloroisocyanurate, potassium dichloroisocyanurate, or a mixture thereof and forming the tablet into a tablet.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9709582A JPS58213714A (en) | 1982-06-07 | 1982-06-07 | Preparation of tablet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9709582A JPS58213714A (en) | 1982-06-07 | 1982-06-07 | Preparation of tablet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58213714A true JPS58213714A (en) | 1983-12-12 |
JPS6352604B2 JPS6352604B2 (en) | 1988-10-19 |
Family
ID=14183069
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9709582A Granted JPS58213714A (en) | 1982-06-07 | 1982-06-07 | Preparation of tablet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58213714A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6289616A (en) * | 1985-10-16 | 1987-04-24 | Kao Corp | Tablet production |
JPH0748598A (en) * | 1993-08-06 | 1995-02-21 | Nissan Chem Ind Ltd | Scale-preventing tablet |
EP0711828A3 (en) * | 1994-11-14 | 1996-11-06 | Unilever Plc | Detergent compositions |
US5916866A (en) * | 1994-11-14 | 1999-06-29 | Lever Brothers Company, Division Of Conopco, Inc. | Preparation of laundry detergent tablets |
JP2012236825A (en) * | 2011-05-10 | 2012-12-06 | Hot Album Tansansen Tablet Inc | Method for producing tablet |
WO2013180048A1 (en) | 2012-05-28 | 2013-12-05 | 株式会社ホットアルバム炭酸泉タブレット | Method for producing tablet, and tablet |
JP2019142936A (en) * | 2016-08-08 | 2019-08-29 | アース製薬株式会社 | Sterilization method |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5239882U (en) * | 1975-09-13 | 1977-03-22 | ||
JPS5343577A (en) * | 1976-09-30 | 1978-04-19 | Mitsubishi Electric Corp | Mean temperature detecting tube |
JPS5756434A (en) * | 1980-09-22 | 1982-04-05 | Kao Corp | Stabilized foamable composition |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5239882B2 (en) * | 1973-08-24 | 1977-10-07 |
-
1982
- 1982-06-07 JP JP9709582A patent/JPS58213714A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5239882U (en) * | 1975-09-13 | 1977-03-22 | ||
JPS5343577A (en) * | 1976-09-30 | 1978-04-19 | Mitsubishi Electric Corp | Mean temperature detecting tube |
JPS5756434A (en) * | 1980-09-22 | 1982-04-05 | Kao Corp | Stabilized foamable composition |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6289616A (en) * | 1985-10-16 | 1987-04-24 | Kao Corp | Tablet production |
JPH0748598A (en) * | 1993-08-06 | 1995-02-21 | Nissan Chem Ind Ltd | Scale-preventing tablet |
EP0711828A3 (en) * | 1994-11-14 | 1996-11-06 | Unilever Plc | Detergent compositions |
US5658874A (en) * | 1994-11-14 | 1997-08-19 | Lever Brothers Company, Division Of Conopco, Inc. | Production of detergent tablet compositions |
US5916866A (en) * | 1994-11-14 | 1999-06-29 | Lever Brothers Company, Division Of Conopco, Inc. | Preparation of laundry detergent tablets |
JP2012236825A (en) * | 2011-05-10 | 2012-12-06 | Hot Album Tansansen Tablet Inc | Method for producing tablet |
WO2013180048A1 (en) | 2012-05-28 | 2013-12-05 | 株式会社ホットアルバム炭酸泉タブレット | Method for producing tablet, and tablet |
KR20150018808A (en) | 2012-05-28 | 2015-02-24 | 가부시키가이샤 홋토아루바무 탄산센 타부렛토 | Method for producing tablet, and tablet |
JP2019142936A (en) * | 2016-08-08 | 2019-08-29 | アース製薬株式会社 | Sterilization method |
Also Published As
Publication number | Publication date |
---|---|
JPS6352604B2 (en) | 1988-10-19 |
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