Kaken Pharmaceutical Company, Ltd.

Dainichiseika Color & Chemicals Mfg. Co., Ltd.

Teraoka Seiko Co., Ltd.

Kazuya Sasaki

Kouji Amemiya

Tadashi Arika

Mamoru Yokoo

Toshiyuki Yamamoto

Tetsuya Maeda

Mituo Takase

Sakae Koshikawa

Rieko Hashimoto

Toshiki Yamada

Ryo Kawamura

Kazuki Watanabe

Tomoki Kaneko

Naoto Kurosaki

Shingo Higuchi

Makoto Yamamoto

Takanobu Naito

Kunio Mori

Fumikatu Saitoh

Masaaki Yokoyama

Katuyuki Ohtuka

Sayaka Tomori

Tatsuzo Murakawa

Eriko Enatsu

Yusuke Suzuki

Akiko Yoshikawa

The present invention relates to a porous layer structure containing a base material and a polyurethane porous layer formed on the base material, wherein a moisture permeability A of the porous layer structure measured by JIS L1099 A-1 (calcium chloride method) is 2000 to 10000 g/(m·24 h), a moisture permeability loss rate obtained by a predetermined formula from a moisture permeability B of the base material alone measured by JIS L1099 A-1 (calcium chloride method) and the moisture permeability A is 75% or less, and a peel strength at a bonding surface between the base material and the polyurethane porous layer is 0.7 kgf/inch or more.

Porous layer constituent and production method therefor

An aqueous polyurethane resin dispersion containing polyurethane resin particles dispersed in water, which contains a nonvolatile component in an amount of 45% by mass or more and in which the polyurethane resin particles contain a polyol component and an isocyanate component, at least 10 mol % or more of the isocyanate component is a linear aliphatic isocyanate component having 4 to 10 carbon atoms, and the volume-average particle size of the polyurethane resin particles is 0.05 to 5 μm.

Aqueous polyurethane resin dispersion and method for producing same, paint, film arrangement, and structure

The present invention relates to a urethane prepolymer having an isocyanate group, a viscosity at 100° C. of 30 to 600 dPa·s, and a thermal softening temperature after moisture curing of 75 to 155° C.

Urethane prepolymer, adhesive, multilayer body and synthetic leather

A weighing and pricing device includes: a processor that executes a registration process for a product to be purchased by a customer; a transceiver that: establishes a connection between a mobile device possessed by the customer and the weighing and pricing device; and upon establishing the connection, receives, from the mobile device, identification information that identifies the mobile device; and a storage that stores information relating to the product and the identification information in association with each other. After the registration process is interrupted, the transceiver receives, from the mobile device, identification information. The processor specifies the product associated with the stored identification information that corresponds to the identification information received after the registration process. The processor recommences the registration process for the specified product.

Weighing and pricing device, sales system, product registration processing method, program, and non-transitory computer-readable medium

A mobile terminal includes: a processor that acquires a type of a product sold by weight; and a transceiver connected to the processor and that establishes intercommunication with a weighing device that weighs the product sold by weight; a storage connected to the processor. The processor causes the transceiver to acquire, from the weighing device, a weight value of the product sold by weight weighed by the weighing device. The processor registers, in the storage, the type of the product and the weight value that corresponds to the type of the product.

Mobile terminal, weighing device, POS terminal, non-transitory computer-readable medium, sales processing system, and sales processing method

Provided is a porous layer structure including a base material (A) and a urethane foam layer provided on the base material (A), wherein the urethane foam layer is a foam layer formed by foaming a urethane prepolymer having an isocyanate group, the urethane foam layer has a density of 0.10 to 0.60 g/cm, and the urethane prepolymer substantially contains no volatile component and satisfies a predetermined composition.

Porous layer structure and method for producing same

A polyurethane prepolymer produced by reacting a polyol and a polyisocyanate, wherein the polyol contains a polyether polyol (A) in an amount of 30% by mass or more, a polyester polyol (B) containing an isophthalic acid-derived structure and a sebacic acid-derived structure as partial structures derived from a dibasic acid in an amount of 30% by mass or more, and a polyester polyol (C) containing only a sebacic acid-derived structure as a partial structure derived from a dibasic acid in an amount of 20% by mass or less, the number-average molecular weight of the polyether polyol (A) is 1100 to 2400, and the ratio of the isocyanate equivalent of the polyisocyanate to the hydroxyl equivalent of the polyol is 2.1 or less.

Polyurethane prepolymer, adhesive and synthetic imitation leather

Amine derivatives having the general formula (I): ##STR1## wherein X is selected from the group consisting of ##STR2## wherein Q is oxygen, sulfur or nitrogen atom, and ##STR3## wherein Q is as above; Y is selected from the group consisting of ##STR4## R.sup.1 is hydrogen atom or an alkyl group; R.sup.2 is hydrogen atom or an alkyl group; R.sup.3 is hydrogen atom, a halogen atom or an alkyl group; R.sup.4 hydrogen atom, an alkyl group, a cycloalkyl group, a halogenated alkyl group or a halogen atom; R.sup.5 is hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, nitro group or hydroxy group; R.sup.5 is attached to an arbitrary position of X, and R.sup.3 or R.sup.4 is attached to an arbitrary position of Y. The amine derivatives (I) are useful as fungicides.

Amine derivatives, processes for preparing the same and fungicides

Amine derivatives having the general formula (I): ##STR1## wherein X is selected from the group consisting of ##STR2## wherein Q is oxygen, sulfur or nitrogen atom, and ##STR3## wherein Q is as above; Y is selected from the group consisting of ##STR4## R.sup.1 is hydrogen atom or an alkyl group; R.sup.2 is hydrogen atom or an alkyl group; R.sup.3 is hydrogen atom, a halogen atom or an alkyl group; R.sup.4 is hydrogen atom, an alkyl group, a cycloalkyl group, a halogenated alkyl group or a halogen atom; R.sup.5 is hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, nitro group or hydroxy group; R.sup.5 is attached to an arbitrary position of X, and R.sup.3 or R.sup.4 is attached to an arbitrary position of Y. The main derivatives (I) are useful as fungicides.

Amine derivatives having the general formula (I): ##STR1## wherein X is selected from the group consisting of ##STR2## Y is selected from the group consisting of ##STR3## R.sup.1 is hydrogen atom or an alkyl group; R.sup.2 is hydrogen atom or an alkyl group; R.sup.3 is hydrogen atom, a halogen atom or an alkyl group; R.sup.4 is hydrogen atom, an alkyl group, a cycloalkyl group, a halogenated alkyl group or a halogen atom; R.sup.5 is hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, nitro group or hydroxy group; R.sup.5 is attached to an arbitrary position of X, and R.sup.3 or R.sup.4 is attached to an arbitrary position of Y. The amine derivatives (I) are useful as fungicides.

Amine derivatives having the general formula (I): ##STR1## wherein X is selected from the group consisting of ##STR2## wherein Q is oxygen, sulfur or nitrogen atom, and ##STR3## wherein Q is as above; Y is selected from the group consisting of ##STR4## R.sup.1 is hydrogen atom or an alkyl group; R.sup.2 is hydrogen atom or an alkyl group; R.sup.3 is hydrogen atom, a halogen atom or an alkyl group; R.sup.4 is hydrogen atom, an alkyl group, a cycloalkyl group, a halogenated alkyl group or a halogen atom; R.sup.5 is hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, nitro group or hydroxy group; R.sup.5 is attached to an arbitrary position of X, and R.sup.3 or R.sup.4 is attached to an arbitrary position of Y. The amine derivatives (I) are useful as fungicides.

Amine derivatives and fungicides containing the same

A cephalosporin compound having the formula: ##STR1## wherein R.sub.1 is a hydroxy group, a lower alkanoyloxy group or a lower alkoxycarbonyloxy group, R.sub.2 is a hydrogen atom, a hydroxy group, a lower alkanoyloxy group or a lower alkoxycarbonyloxy group, R.sub.3 is a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkenyl group, a lower alkoxy group or --CH.sub.2 R.sub.7 (wherein R.sub.7 is a hydrogen atom, an azido group, a lower alkanoyloxy group, a carbamoyloxy group, a substituted or unsubstituted pyridinium group or a substituted or unsubstituted heterocyclic thio group), R.sub.4 is a hydrogen atom or a carboxy-protecting group, each of R.sub.5 and R.sub.6 is a hydrogen atom or a lower alkyl group, or R.sub.5 and R.sub.6 form a cycloalkylidene group together with the carbon atom to which they are attached, and m is 0 to 1, or a pharmaceutically acceptable salt thereof.

Cephalosporin compounds

An antifungal and antibacterial imidazole derivative represented by the general formula I or a biologically acceptable acid addition salt thereof: ##STR1## where Ar is a phenyl group which may be substituted by alkyl having from 1 to 6 carbon atoms, alkoxy having from 1 to 4 carbon atoms, alkylamino having from 1 to 4 carbon atoms, alkoxy carbonyl having from 1 to 4 carbon atoms, phenyl, halogen or hydroxyl; a naphthyl group; a furyl group; or a thienyl group which may be substituted by halogen or alkyl having from 1 to 4 carbon atoms, and R is an alkyl group having from 1 to 10 carbon atoms; an alkenyl group having from 1 to 6 carbon atoms; or a phenylalkyl group which may be substituted by halogen.

Growing community of inventors

Higashikurume, Japan

Kazuya Sasaki