Detail of > 112-92-5
- MSDS Download

- CAS Number:
- 112-92-5
- Name:
1-Octadecanol
- Formula:
- C18H38O
- Molecular Structure:

- Synonyms:
- 1-Hydroxyoctadecane;1-Stearyl alcohol;Adol 62;Adol 64;Adol 68;Alfol 18;Alfol 18NF;Atalco S;CO 1895;CO 1895F;CO 1897;Cachalot S 43;Conol 1675;Conol 30F;Conol 30S;Conol 30SS;Crodacol S;Crodacol S 70;Crodacol S 95;Crodacol S 95 NF;Hainol18SS;Hyfatol 18-95;Hyfatol 18-98;Kalchol 8098;Kalcohl 80;Kalcohl 8098;Kalcohl 8099;Kalcol 8098;Lanette 18;Lanette 18DEO;Lanol S;Laurex 18;Lorol28;Lorol C 18;NSC 5379;Octadecanol;Octadecyl alcohol;Rofamol;Sipol S;Siponol S;Siponol SC;Stearic alcohol;Stearol;Stearyl alcohol;Steraffine;Tego alkanol 18;VLTN 6;n-Octadecanol;n-Octadecyl alcohol;
- Molecular Weight:
- 270.56
- EINECS:
- 204-017-6
- Density:
- 0.837 g/cm3
- Melting Point:
- 55-58 °C
- Boiling Point:
- 334.3 °C at 760 mmHg
- Flash Point:
- 138.7 °C
- Solubility:
- insoluble in water
- Appearance:
- White flakes
- Safety:
- 24/25Details
- Transport Information:
- UN 1986
- Deleted CAS:
- 193766-48-2|8014-37-7|8032-19-7|8032-21-1|8034-90-0
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Reference
- Herbicidal concentrated emulsions
- Herbicidal concentrated emulsions. Valange, Baudouin Maurice (Monsanto Co. , USA).Several substances are used for example 2303-16-4 and 9004-99-3 which are their cas registry numbers. Eur. Pat. Appl. EP 93105 A2 2 Nov 1983, 18 pp. DESIGNATED STATES: R: BE, DE, FR, GB, IT, NL, SE. (English). (European Patent Organization). CODEN: EPXXDW. CLASS: IC: A01N025-04; A01N037-22; A01N037-26; A01N047-12. APPLICATION: EP 83-870043 15 Apr 1983. PRIORITY: US 82-369697 19 Apr 1982. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical Bioregulators) Formulations comprised of a 2-haloacetanilide or thiocarbamate herbicide (40-65% by wt.) with a soln. point of £25° in water, a hydrocarbon solvent (15-30%), emulsifier (2.5-10.0%), straight-chain alc. coemulsifier, and water (balance) contg. an appropriate salt (4-20% by wt. of water) are concd. emulsions which are storage-stable at low temps. Thus, a formulation comprised of alachlor [15972-60-8] 42.8, monochlorobenzene [108-90-7] 20.0, coemulsifiers 1-tetradecanol [112-72-1] 0.3, 1-hexadecanol [36653-82-4] 2.7, 1-octadecanol [112-92-5] 1.0, emulsifiers Atlox G7596HJ [88527-92-8] 2.5% by wt. with the balance being water contg. 15% CaCl2 was stable at low temp. in both dild. (0° for 24 and 72 h) and concd. (-9° for 2 wk) form. .
- Antistatic methacrylic resin compositions
- Antistatic methacrylic resin compositions. (Asahi Chemical Industry Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 59012957 A2 23 Jan 1984 Showa, 6 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C08L033-12; C08K005-05; C08K005-10.There are some reagents with their cas registry numbers 56-81-5 and 30396-85-1 are used in this study. APPLICATION: JP 82-123377 15 Jul 1982. DOCUMENT TYPE: Patent CA Section: 37 (Plastics Manufacture and Processing) The resin compns. contain methacrylic resins 100, highly pure glycerin monolaurate (I) [27215-38-9] 1.0-4.0, and C13-22 alkanols and/or glycerin [56-81-5] 0.05-1 part. Thus, moldings prepd. from 2:98 Me acrylate-Me methacrylate copolymer [9011-87-4] 100, I 4, stearyl alc. [112-92-5] 0.5, and glycerin 0.2 part had surface resistance 1.5 ′ 1011 W, half-life 2.0 s, and heat distortion temp. 70°, compared with 2.6 ′ 1013, 26, and 70°, resp., for moldings contg. glycerin monostearate in place of I. .
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