JP2009527469A5 - - Google Patents
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- JP2009527469A5 JP2009527469A5 JP2008554434A JP2008554434A JP2009527469A5 JP 2009527469 A5 JP2009527469 A5 JP 2009527469A5 JP 2008554434 A JP2008554434 A JP 2008554434A JP 2008554434 A JP2008554434 A JP 2008554434A JP 2009527469 A5 JP2009527469 A5 JP 2009527469A5
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- Prior art keywords
- propanediol
- extract
- mixtures
- extracts
- acid
- Prior art date
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Description
次の酸およびその塩またはアルキルエステルは特に有用である。酢酸、酪酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、アラキジン酸、アジピン酸、安息香酸、カプリル酸、マレイン酸、パルミチン酸、セバシン酸、アルキドン酸、ユーシン酸、パルミトレイン酸、ペンタデカン酸、ヘプタデカン酸、ノンデカン酸、オクタデカテトラエン酸、エイコサテトラエン酸、エイコサペンタエン酸、ドコサペンタエン酸、テトラコサペンタエン酸、テトラヘキサエン酸、ドコサヘキセン酸、(アルファ)−リノレン酸、ドコサヘキサエン酸、エイコサペンタエン酸、リノール酸、アラキドン酸、オレイン酸、エルシン酸、蟻酸、プロピオン酸、吉草酸、カプロン酸、カプリン酸、マロン酸、コハク酸、グルタル酸、アジピン酸、ピメル酸、スベリン酸、アゼライン酸、酒石酸、クエン酸、サリチル酸、アセチル−サリチル酸、ペラルゴン酸、ベヘン酸、セロチン酸、マーガリン酸、モンタン酸、メリシン酸、ラセロン酸、セロメリシン酸、ゲディン酸、セロプラスチン酸、ウンデシレン酸、リシノレン酸、およびエラエオステアリン酸さらにはこのような酸の混合物。好適な有機酸のより好ましいリストは、酢酸、アジピン酸、安息香酸、マレイン酸、セバシン酸およびこのような酸の混合物である。本発明で有用な炭素鎖中に8〜40個の炭素を含有する一般的に酸を意味する好適な「脂肪酸」のより好ましいリストは、酪酸、吉草酸、カプロン酸、カプリル酸、ペラルゴン酸、カプリン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、アラキジン酸、ベヘン酸、セロチン酸、オレイン酸、リノール酸、リノレン酸、マーガリン酸、モンタン酸、メリシン酸、ラセロン酸、セロメリシン酸、ゲディン酸、セロプラスチン酸、およびこのような酸の混合物を含む。
これらの酸の中で、最も好ましいこれらの酸およびその塩およびアルキルエステルは、ステアリン酸、ラウリン酸、パルミチン酸、オレイン酸、2−エチルヘキサン酸および12−ヒドロキシステアリン酸およびこのような酸の混合物である。
これらの酸の中で、最も好ましいこれらの酸およびその塩およびアルキルエステルは、ステアリン酸、ラウリン酸、パルミチン酸、オレイン酸、2−エチルヘキサン酸および12−ヒドロキシステアリン酸およびこのような酸の混合物である。
Claims (19)
- (a)1,3−プロパンジオールのエステルを提供し;
(b)1,3−プロパンジオールエステルと天然の抽出物ソースを混合し、抽出物ソースからエステルへと抽出物を抽出し;
(c)エステルによる抽出物から抽出物ソースを分離する
ことを包含する天然の抽出物ソースから抽出物を抽出する方法であって、
1,3−プロパンジオールが、生物学的に誘導され、少なくとも85%の生物由来炭素を有し、
1,3−プロパンジオールのエステルが、式R 1 −C(=O)−O−CH 2 −CH 2 −CH 2 −OHまたは式R 1 −C(=O)−O−CH 2 −CH 2 −CH 2 −O−C(=O)−R 2 (ここで、R 1 およびR 2 は1〜40個の炭素鎖長の線状または分岐炭素鎖である)を有する、
前記方法。 - さらに、1,3−プロパンジオールを、前記エステルおよび前記抽出物ソースと混合することを包含する請求項1記載の方法。
- 1,3−プロパンジオールは少なくとも95%の生物由来炭素を有する請求項2記載の方法。
- R1およびR2は同じ炭素鎖である請求項1〜3のいずれかに記載の方法。
- エステルは
i.プロパンジオールジステアレート、モノステアレートおよびその混合物;
ii.プロパンジオールジラウレート、モノラウレートおよびその混合物;
iii.プロパンジオールジオレエート、モノオレエートおよびその混合物;
iv.プロパンジオールジバレレート、モノバレレートおよびその混合物;
v.プロパンジオールジカプリレート、モノカプリレートおよびその混合物;
vi.プロパンジオールジミリステート、モノミリステートおよびその混合物;
vii.プロパンジオールジパルミテート、モノパルミテートおよびその混合物;
viii.プロパンジオールジベヘネート、モノベヘネートおよびその混合物;
ix.プロパンジオールアジペート;
x.プロパンジオールマレエート;
xi.プロパンジオールジベンゾエート;
xii.プロパンジオールジアセテート;
xiii.プロパンジオールビス(エチルヘキサノエート);および
xiv.その混合物
からなる群の1以上の要素から選択される請求項1〜4のいずれかに記載の方法。 - 1,3−プロパンジオールのエステルがビス(エチルヘキサノエート)である請求項5記載の方法。
- 抽出物はエッセンシャルオイルである請求項1〜6のいずれかに記載の方法。
- 抽出物はハーバル抽出物である請求項1〜6のいずれかに記載の方法。
- 抽出物が、エッセンシャルオイル、ハーバル抽出物、植物抽出物、野菜抽出物、海洋性抽出物、藻類抽出物、菌類抽出物、プランクトン抽出物、魚抽出物、たんぱく質抽出物、脂質抽出物、動物抽出物および牛乳抽出物からなる群より選択される請求項1〜6のいずれかに記載の方法。
- 天然の抽出物ソースが、植物、野菜、海洋性ソース、藻類、菌類、プランクトン、魚、動物または牛乳から選択される請求項1〜9のいずれかに記載の方法。
- 抽出溶媒または希釈剤としての1,3−プロパンジオールのエステルと抽出物を含有する組成物であって、
1,3−プロパンジオールは生物学的に誘導され、少なくとも85%の生物由来炭素を有し、
1,3−プロパンジオールのエステルが、式R 1 −C(=O)−O−CH 2 −CH 2 −CH 2 −OHまたは式R 1 −C(=O)−O−CH 2 −CH 2 −CH 2 −O−C(=O)−R 2 (ここで、R 1 およびR 2 は1〜40個の炭素鎖長の線状または分岐炭素鎖である)を有し、
抽出物が、天然の抽出物ソースから抽出されたものであり、
組成物が石油由来グリコールを含む組成物より環境への影響が少ない、
前記組成物。 - 1,3−プロパンジオールは100%生物由来炭素を有する請求項11記載の組成物。
- R1およびR2はアルケン、アミド、アミン、カルボニル、カルボン酸、ハライド、ヒドロキシル基、エーテル、アルキルエーテル、スルフェートおよびエーテルスルフェートからなる群から選択される1以上の官能基を有する請求項11または12記載の組成物。
- R1およびR2は同じ炭素鎖である請求項11〜13のいずれかに記載の組成物。
- エステルは
i.プロパンジオールジステアレート、モノステアレートおよびその混合物;
ii.プロパンジオールジラウレート、モノラウレートおよびその混合物;
iii.プロパンジオールジオレエート、モノオレエートおよびその混合物;
iv.プロパンジオールジバレレート、モノバレレートおよびその混合物;
v.プロパンジオールジカプリレート、モノカプリレートおよびその混合物;
vi.プロパンジオールジミリステート、モノミリステートおよびその混合物;
vii.プロパンジオールジパルミテート、モノパルミテートおよびその混合物;
viii.プロパンジオールジベヘネート、モノベヘネートおよびその混合物;
ix.プロパンジオールアジペート;
x.プロパンジオールマレエート;
xi.プロパンジオールジベンゾエート;
xii.プロパンジオールジアセテート;
xiii.プロパンジオールビス(エチルヘキサノエート);および
xiv.その混合物
からなる群から選択される請求項11〜14のいずれかに記載の組成物。 - 1,3−プロパンジオールのエステルがビス(エチルヘキサノエート)である請求項15に記載の組成物。
- 天然の抽出物ソースが、植物、野菜、海洋性ソース、藻類、菌類、プランクトン、魚、動物または牛乳から選択される請求項11〜16のいずれかに記載の組成物。
- 抽出物は、エッセンシャルオイル、ハーバル抽出物、植物抽出物、野菜抽出物、たんぱく質抽出物、脂質抽出物、海洋性抽出物、藻類抽出物、菌類抽出物、プランクトン抽出物、魚抽出物、動物抽出物および牛乳抽出物からなる群から選択される請求項11〜17のいずれかに記載の組成物。
- さらに、生物学的に誘導された1,3−プロパンジオールを含有する請求項11〜18のいずれかに記載の組成物。
Applications Claiming Priority (25)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77211006P | 2006-02-10 | 2006-02-10 | |
US77247106P | 2006-02-10 | 2006-02-10 | |
US77211206P | 2006-02-10 | 2006-02-10 | |
US77219306P | 2006-02-10 | 2006-02-10 | |
US77211106P | 2006-02-10 | 2006-02-10 | |
US77219406P | 2006-02-10 | 2006-02-10 | |
US77212006P | 2006-02-10 | 2006-02-10 | |
US60/772,471 | 2006-02-10 | ||
US60/772,110 | 2006-02-10 | ||
US60/772,112 | 2006-02-10 | ||
US60/772,194 | 2006-02-10 | ||
US60/772,111 | 2006-02-10 | ||
US60/772,120 | 2006-02-10 | ||
US60/772,193 | 2006-02-10 | ||
US84694806P | 2006-09-25 | 2006-09-25 | |
US60/846,948 | 2006-09-25 | ||
US85392006P | 2006-10-24 | 2006-10-24 | |
US60/853,920 | 2006-10-24 | ||
US85926406P | 2006-11-15 | 2006-11-15 | |
US60/859,264 | 2006-11-15 | ||
US87270506P | 2006-12-04 | 2006-12-04 | |
US60/872,705 | 2006-12-04 | ||
US88082407P | 2007-01-17 | 2007-01-17 | |
US60/880,824 | 2007-01-17 | ||
PCT/US2007/003850 WO2007095262A2 (en) | 2006-02-10 | 2007-02-12 | Bio-derived 1,3-propanediol and its conjugate esters as natural and non irritating solvents |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014004699A Division JP5916773B2 (ja) | 2006-02-10 | 2014-01-15 | バイオマス誘導された抽出物、フレグランス濃縮物、およびオイル用の天然非刺激性溶剤としての生物誘導された1,3−プロパンジオールおよびその共役エステル |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2009527469A JP2009527469A (ja) | 2009-07-30 |
JP2009527469A5 true JP2009527469A5 (ja) | 2014-09-04 |
JP5622359B2 JP5622359B2 (ja) | 2014-11-12 |
Family
ID=38372098
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008554434A Active JP5622359B2 (ja) | 2006-02-10 | 2007-02-12 | バイオマス誘導された抽出物、フレグランス濃縮物、およびオイル用の天然非刺激性溶剤としての生物誘導された1,3−プロパンジオールおよびその共役エステル |
JP2013168759A Pending JP2014027937A (ja) | 2006-02-10 | 2013-08-15 | 再生ベースの生分解性1,3−プロパンジオールを含む生分解性組成物 |
JP2014004699A Active JP5916773B2 (ja) | 2006-02-10 | 2014-01-15 | バイオマス誘導された抽出物、フレグランス濃縮物、およびオイル用の天然非刺激性溶剤としての生物誘導された1,3−プロパンジオールおよびその共役エステル |
JP2015022228A Active JP6006817B2 (ja) | 2006-02-10 | 2015-02-06 | 再生ベースの生分解性1,3−プロパンジオールを含む生分解性組成物 |
JP2016239955A Active JP6243999B2 (ja) | 2006-02-10 | 2016-12-12 | 再生ベースの生分解性1,3−プロパンジオールを含む生分解性組成物 |
Family Applications After (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013168759A Pending JP2014027937A (ja) | 2006-02-10 | 2013-08-15 | 再生ベースの生分解性1,3−プロパンジオールを含む生分解性組成物 |
JP2014004699A Active JP5916773B2 (ja) | 2006-02-10 | 2014-01-15 | バイオマス誘導された抽出物、フレグランス濃縮物、およびオイル用の天然非刺激性溶剤としての生物誘導された1,3−プロパンジオールおよびその共役エステル |
JP2015022228A Active JP6006817B2 (ja) | 2006-02-10 | 2015-02-06 | 再生ベースの生分解性1,3−プロパンジオールを含む生分解性組成物 |
JP2016239955A Active JP6243999B2 (ja) | 2006-02-10 | 2016-12-12 | 再生ベースの生分解性1,3−プロパンジオールを含む生分解性組成物 |
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Country | Link |
---|---|
US (26) | US20070200087A1 (ja) |
EP (3) | EP2007210A4 (ja) |
JP (5) | JP5622359B2 (ja) |
CN (2) | CN105175257A (ja) |
ES (1) | ES2797782T3 (ja) |
WO (2) | WO2008123845A2 (ja) |
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- 2007-02-12 CN CN201510639438.9A patent/CN105175257A/zh active Pending
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