[ CAS No. 96-20-8 ] {[proInfo.proName]}

Name: 96-20-8|2-Aminobutan-1-ol|98%
Brand: Ambeed
SKU: A456870
Rating: 90 (29 reviews)

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Cat. No.: {[proInfo.prAm]}

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Quality Control of [ 96-20-8 ]

COA NMR CNMR HPLC LC-MS

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SDS Specification

Alternatived Products of [ 96-20-8 ]

Product Details of [ 96-20-8 ]

CAS No. :	96-20-8	MDL No. :	MFCD00008095
Formula :	C₄H₁₁NO	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	JCBPETKZIGVZRE-UHFFFAOYSA-N
M.W :	89.14	Pubchem ID :	22129
Synonyms :

Safety of [ 96-20-8 ]

Signal Word:	Danger	Class:	8
Precautionary Statements:	P501-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310	UN#:	3267
Hazard Statements:	H314	Packing Group:	Ⅲ
GHS Pictogram:

Application In Synthesis of [ 96-20-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 96-20-8 ]
Downstream synthetic route of [ 96-20-8 ]

[ 96-20-8 ] Synthesis Path-Upstream 1~16

1
[ 2835-81-6 ]
[ 96-20-8 ]
[ 22621-37-0 ]

Yield	Reaction Conditions	Operation in experiment
90%	With ammonium hydroxide In ethanol	Production of (+)-2-Amino-1-butanol EXAMPLE 9 1.8 g of L-2-aminobutyric acid as obtained in Example 5 was dispersed in 30 ml of ethanol and dry hydrogen chloride gas was bubbled through the dispersion until the L-2-aminobutyric acid was completely dissolved to form a homogeneous solution, and then the solution was refluxed for 4 hours. After cooling, the ethanol was removed under reduced pressure. The crystals obtained were dissolved by adding aqueous ammonia while cooling and then extracted with diethyl ether. The extract was dried with magnesium sulfate and distilled under reduced pressure, and thus 2.0 g of a L-2-aminobutyric acid ethyl ester fraction (b.p. 66°-67°C/18 mm Hg) was obtained. The yield was 90percent. (α)_D²⁷ = +17.8° +- 1° (C = 5.6, ethanol).

Reference： [1] Patent: US3979457, 1976, A,

2
[ 609-31-4 ]
[ 96-20-8 ]

Reference： [1] Patent: US4924029, 1990, A,
[2] Patent: US4924029, 1990, A,
[3] Journal of Organic Chemistry, 1943, vol. 8, p. 11
[4] Journal of Organic Chemistry, 1943, vol. 8, p. 11
[5] Chem. Zentralbl., 1902, vol. 73, # I, p. 717
[6] Industrial and Engineering Chemistry, 1948, vol. 40, p. 507
[7] Tetrahedron, 1990, vol. 46, # 21, p. 7403 - 7412
[8] Tetrahedron, 1990, vol. 46, # 21, p. 7403 - 7412

3
[ 193086-15-6 ]
[ 96-20-8 ]

Reference： [1] Tetrahedron Letters, 2010, vol. 51, # 39, p. 5131 - 5133

4
[ 5339-83-3 ]
[ 96-20-8 ]

Reference： [1] Synthesis, 2003, # 13, p. 1965 - 1967

5
[ 72784-43-1 ]
[ 96-20-8 ]

Reference： [1] Patent: EP3424928, 2019, A1,

6
[ 2835-81-6 ]
[ 96-20-8 ]

Reference： [1] Monatshefte fuer Chemie, 1953, vol. 84, p. 1097
[2] Doklady Chemistry, 1972, vol. 203, p. 200 - 203[3] Dokl. Akad. Nauk SSSR Ser. Khim., 1972, vol. 203, p. 106 - 109
[4] Doklady Chemistry, 1972, vol. 203, p. 240 - 243[5] Dokl. Akad. Nauk SSSR Ser. Khim., 1972, vol. 203, p. 354 - 357

7
[ 91028-76-1 ]
[ 96-20-8 ]

Reference： [1] Journal of the American Chemical Society, 1954, vol. 76, p. 1231,1233

8
[ 860763-66-2 ]
[ 96-20-8 ]

Reference： [1] Annales de Chimie (Cachan, France), 1912, vol. <8>26, p. 270

9
[ 7682-18-0 ]
[ 96-20-8 ]

Reference： [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1979, p. 1230 - 1236

10
[ 106-88-7 ]
[ 96-20-8 ]
[ 13552-21-1 ]
[ 584-03-2 ]

Reference： [1] Physical Chemistry Chemical Physics, 2018, vol. 20, # 3, p. 1583 - 1590

11
[ 7062-04-6 ]
[ 96-20-8 ]

Reference： [1] Pharmaceutical Chemistry Journal, 1978, vol. 12, # 4, p. 491 - 493[2] Khimiko-Farmatsevticheskii Zhurnal, 1978, vol. 12, # 4, p. 77 - 79

12
[ 153363-52-1 ]
[ 96-20-8 ]

Reference： [1] Gazzetta Chimica Italiana, 1993, vol. 123, # 10, p. 549 - 552

13
[ 7647-01-0 ]
[ 860763-66-2 ]
[ 96-20-8 ]

Reference： [1] Annales de Chimie (Cachan, France), 1912, vol. <8>26, p. 270

14
[ 96-20-8 ]
[ 5856-63-3 ]

Reference： [1] Synthesis, 2003, # 13, p. 1965 - 1967
[2] Journal of the American Chemical Society, 1954, vol. 76, p. 2801
[3] Acta Chemica Scandinavica (1947-1973), 1962, vol. 16, p. 71 - 77
[4] Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1961, vol. 253, p. 2704 - 2705
[5] Journal of Heterocyclic Chemistry, 1970, vol. 7, p. 1407 - 1411

15
[ 96-20-8 ]
[ 5856-63-3 ]
[ 5856-62-2 ]

Reference： [1] Patent: WO2010/148191, 2010, A2, . Location in patent: Page/Page column 45-49; 59
[2] New Journal of Chemistry, 2013, vol. 37, # 12, p. 4018 - 4024

16
[ 96-20-8 ]
[ 18162-48-6 ]
[ 811841-81-3 ]

Reference： [1] Journal of the American Chemical Society, 2018, vol. 140, # 16, p. 5322 - 5325

[ 96-20-8 ] Synthesis Path-Downstream 1~18

1
[ 96-20-8 ]
[ 3913-17-5 ]
2-(4,8-dimethyl-[2]quinolylamino)-butan-1-ol [ No CAS ]

Reference： [1]Journal of the American Chemical Society,1949,vol. 71,p. 3221

2
[ 96-20-8 ]
[ 6306-61-2 ]
[ 26805-92-5 ]

Reference： [1]Journal of medicinal and pharmaceutical chemistry,1962,vol. 5,p. 835 - 845

3
[ 96-20-8 ]
[ 3449-48-7 ]
[ 118499-11-9 ]

Reference： [1]Pharmaceutical Chemistry Journal,1988,vol. 22,p. 780 - 785
Khimiko-Farmatsevticheskii Zhurnal,1988,vol. 22,p. 1217 - 1222

4
[ 67-56-1 ]
[ 597-09-1 ]
Raney nickel [ No CAS ]
[ 96-20-8 ]
[ 115-70-8 ]

Reference： [1]Industrial and Engineering Chemistry,1940,vol. 32,p. 35

5
[ 96-20-8 ]
[ 1070-70-8 ]
polymer, Mw = 11520, PDI = 3.60; monomer(s): 1,4-butanediol diacrylate; 2-amino-butan-1-ol [ No CAS ]

Reference： [1]Journal of the American Chemical Society,2001,vol. 123,p. 8155 - 8156

6
[ 96-20-8 ]
[ 98-59-9 ]
[ 304460-78-4 ]

Reference： [1]Tetrahedron Letters,2009,vol. 50,p. 6886 - 6890
[2]Tetrahedron Letters,2009,vol. 50,p. 648 - 650
[3]Advanced Synthesis and Catalysis,2007,vol. 349,p. 1873 - 1876
[4]Tetrahedron,2008,vol. 64,p. 6461 - 6474
[5]Organic Letters,2018,vol. 20,p. 7419 - 7423

7
[ 96-20-8 ]
[ 13600-42-5 ]
C₁₁H₁₁ClF₃N₃O [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
55%	With diisopropylamine; at 70℃;sealed tube;	Example VIII. Synthesis of 2-chloro-6-[5-ethyl-2-(2-pyridyl)oxazolidin-3-yl]-4- (trifluoromethyl) pyridine-3-carbonitrile (Compound 17).; Step 1 : Synthesis of 2-chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl)pyridine- 3-carbonitrile.; Neat 3-cyano-2,6-dichloro-4-trifiuoromethylpyridine (0.641 g, 6 mmol) was added by pipette at a dropwise rate over 3 minutes to 2-aminobutanol (1.5 g, 6 mmol). Di-isopropylamine (0.9 g, 7 mmol) was added after 10 minutes and the resultant mixture was heated in a sealed tube at 70 C for 30 minutes to selectively displace the chlorine at position 6 before quenching in ice-cold water and extracted with dichloromethane. Organic extracts were washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was washed with diethylether and the resultant solid was used in the next step without further purification. 2-Chloro-6-(2-hydroxybutylarnino)-4-(trifluoromethyl) pyridine-3- carbonitrile was isolated in 55 % yield. 1HNMR (CDCl3, 400 MHz) delta / ppm 6.64 (s, IH), 5.96 (br, IH), 3.78 (br, IH), 3.32 (br, IH), 1.94 (br d, J = 4.1 Hz, IH), 1.65 - 1.50 (m, 4H), 1.02 (t, J = 7.5 Hz, 3H).

Reference： [1]Patent: WO2010/126580,2010,A1 .Location in patent: Page/Page column 21-22

8
[ 96-20-8 ]
[ 873-42-7 ]
[ 1617545-91-1 ]

Yield	Reaction Conditions	Operation in experiment
600 mg	In neat (no solvent); at 120℃; for 1h;Microwave irradiation;	Step 1: Preparation of 2-(3-amino-6-chloro-pyrazin-2-ylamino)-butan-l-ol Neat reaction between 3, 5-dichloro-pyrazin-2-ylamine (1 g, 4.6 mmol) and 2-amino- butan- l-ol (1.23 g, 13.8 mmol) was carried out under microwave at 120 C for 1 hour. Then the mixture was partitioned between EtOAc and brine. The aqueous layer was separated and then extracted with EtOAc. The combined organic layers were concentrated, and then the residue was purified by column chromatography to give 600 mg of 2-(3-amino-6-chloro-pyrazin-2-ylamino)- butan-l-ol.

Reference： [1]Patent: WO2014/106606,2014,A1 .Location in patent: Page/Page column 59

9
[ 96-20-8 ]
[ 37585-16-3 ]
8-chloro-3-ethyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine [ No CAS ]

Reference： [1]European Journal of Organic Chemistry,2015,vol. 2015,p. 1068 - 1074

10
[ 96-20-8 ]
[ 52449-43-1 ]
C₁₂H₁₆ClNO₂ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	at 140℃;	General procedure: The carboxylic esters (0.08 mol) were respectively heated with racemic 2-aminobutanol (0.08 mol) in a 50-ml, round-bottomed flask at 140 C. The reaction was followed bythin-layer chromatography (TLC). After the reaction, the residue was then recrystallized from chloroform-hexane.

Reference： [1]Synthetic Communications,2016,vol. 46,p. 956 - 962

11
[ 96-20-8 ]
[ 2421-28-5 ]
C₂₅H₂₄N₂O₇ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	for 3h;Reflux;	In a reaction vessel, 3.22 g (9.99 mmol) of BTDA, 1.78 g (19.98 mmol) of 2-amino-1-butanol and 10 ml of EDM were added, And refluxed for 3 hours. After completion of the reaction, EDM and water generated in the reaction were removed. Subsequently, 20 ml of methyl ethyl ketone, 0.01 g (0.01 mmol) of dibutyltin dilaurate and 0.01 g (0.10 mmol) of 4-methoxyphenol were mixed in the reaction vessel. To this was added dropwise 3.38 g (23.98 mmol) of 2-isocyanatoethyl acrylate. After completion of the dropwise addition, the mixture was stirred at 45 C. for 2 hours. After the reaction, in order to react excess 2-isocyanatoethyl acrylate, 2 ml of methanol was poured into the reaction solution and the mixture was stirred on an ice bath for 30 minutes. After stirring, the solvent was removed to obtain 8.23 g of acrylic imide 2.

Reference： [1]Patent: JP2017/202988,2017,A .Location in patent: Paragraph 0094

12
[ 96-20-8 ]
[ 2420-87-3 ]
C₂₄H₂₄N₂O₆ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	for 3h;Reflux;	To the reaction vessel, 1.56 g (5.29 mmol) of BPDA, 0.95 g (10.58 mmol) of 2-amino-1-butanol and 10 ml of GBL were added, And refluxed for 3 hours. After completion of the reaction, GBL and water generated by the reaction were removed. Subsequently, 20 ml of methyl ethyl ketone, 0.01 g (0.01 mmol) of dibutyltin dilaurate and 0.01 g (0.10 mmol) of 4-methoxyphenol were mixed in the reaction vessel. To this was added dropwise 1.80 g (12.73 mmol) of 2-isocyanatoethyl acrylate. After completion of the dropwise addition, the mixture was stirred at 45 C. for 2 hours. After the reaction, in order to react excess 2-isocyanatoethyl acrylate, 2 ml of methanol was poured into the reaction solution and the mixture was stirred on an ice bath for 30 minutes. After stirring, the solvent was removed to obtain 4.26 g of acrylic imide 3.

Reference： [1]Patent: JP2017/202988,2017,A .Location in patent: Paragraph 0095

13
[ 96-20-8 ]
[ 38103-06-9 ]
C₃₉H₃₈N₂O₈ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	for 3h;Reflux;	3.73 g (7.16 mmol) of BSAA, 1.28 g (14.31 mmol) of 2-amino-1-butanol and 10 ml of EDM were added to the reaction vessel and refluxed for 3 hours. After completion of the reaction, water generated by EDM and reaction was removed. Subsequently, 20 ml of methyl ethyl ketone, 0.01 g (0.01 mmol) of dibutyltin dilaurate and 0.01 g (0.10 mmol) of 4-methoxyphenol were mixed in the reaction vessel. To this was added dropwise 2.42 g (17.17 mmol) of 2-isocyanatoethyl acrylate. After completion of the dropwise addition, the mixture was stirred at 45 C for 2 hours. After the reaction, in order to react excess 2-isocyanatoethyl acrylate, 2 ml of methanol was poured into the reaction solution and the mixture was stirred on an ice bath for 30 minutes. After stirring, the solvent was removed to obtain 7.36 g of acrylic imide 5 .

Reference： [1]Patent: JP2017/202988,2017,A .Location in patent: Paragraph 0097

14
[ 96-20-8 ]
[ 1823-59-2 ]
C₂₄H₂₄N₂O₇ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	In 5,5-dimethyl-1,3-cyclohexadiene; for 3h;Dean-Stark; Reflux;	To the reaction vessel, 3.18 g (10.24 mmol) of ODPA, 1.83 g (20.47 mmol) of 2-amino-1-butanol and 40 ml of xylene were added, a Dean Stark apparatus was attached and refluxed for 3 hours while removing water generated by the reaction. After completion of the reaction, xylene was removed. continue, in the reaction vessel, 20 ml of methyl ethyl ketone, 0.01 g (0.01 mmol) of dibutyltin dilaurate and 0.01 g (0.10 mmol) of 4-methoxyphenol was mixed. To this was added dropwise 3.47 g (24.59 mmol) of 2-isocyanatoethyl acrylate. After completion of the dropwise addition, Followed by stirring at 45 C. for 2 hours. After the reaction, to react excess 2-isocyanatoethyl acrylate, 2 ml of methanol was poured into the reaction solution, and the mixture was stirred on an ice bath for 30 minutes. After stirring, by removing the solvent, 7.79 g of acrylic imide 1 was obtained.

Reference： [1]Patent: JP2017/202988,2017,A .Location in patent: Paragraph 0093

15
[ 96-20-8 ]
[ 18162-48-6 ]
[ 811841-81-3 ]

Reference： [1]Journal of the American Chemical Society,2018,vol. 140,p. 5322 - 5325

16
[ 72784-43-1 ]
[ 96-20-8 ]

Yield	Reaction Conditions	Operation in experiment
	With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20℃; for 18.0h;Inert atmosphere;	methyl 1-aminocyclopropylcarboxylate (800mg, 6.96mmol) and 20mLtetrahydrofuran were added into a 100mL three-neck flask, the mixture was cooled to 0C under argon atmosphere,then a solution of lithium aluminum hydride in tetrahydrofuran (15mL, 7.5mmol) was added dropwise. After completionof the addition, the reaction solution was stirred at room temperature for 18 hours. After completion of the reaction, thereaction solution was quenched, filtered through celite, dried over anhydrous sodium sulfate and concentrated to give800mg crude product, which was used directly in the next step.

Reference： [1]Patent: EP3424928,2019,A1 .Location in patent: Paragraph 0532

17
[ 96-20-8 ]
[ 66222-29-5 ]
1-((tributylstannyl)methoxy)butan-2-amine [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
88%		A procedure from the literature was modified afollows:8 Sodium hydride (80 mg of a 60% suspension in mineral oil, 1.97 mmol, 1.30 equiv) waswashed with pentane (3 x 3 mL) and suspended in DMF (6 mL). The suspension was cooled to 0 Cand 2-amino-1-butanol (26; 144 μL, 1.52 mmol, 1.00 equiv) in DMF (4 mL) was added dropwise over10 min. The resulting suspension was allowed to warm to r.t.. After 60 min, the reaction mixture wasre-cooled to 0 C and <strong>[66222-29-5]tributyl(iodomethyl)stannane</strong> 5 (785 mg, 1.82 mmol, 1.20 equiv) was addeddropwise over 5 min. The resulting suspension was allowed to warm to r.t. over 3 h and stirred at r.t.for 3 h. The reaction mixture was cooled to 0 C and slowly quenched with sat aq NH4Cl (20 mL).EtOAc (20 mL) was added, the layers were separated and the aqueous layer was extracted with EtOAc(3 x 30 mL). The combined organic layers were washed with H2O (5 x 30 mL), brine (3 x 20 mL),dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. Purification by flashchromatography (EtOAc) afforded SnAP 3-Et M 27 (524 mg, 88% yield) as a pale yellow oil. IR (thinfilm): ν 2960, 2925, 2870, 2855, 1456, 1091 cm-1; 1H NMR (400 MHz, CDCl3): δ 3.79 - 3.64 (m,2H), 3.29 (dd, J = 9.0, 3.8 Hz, 1H), 3.09 (dd, J = 9.0, 7.7 Hz, 1H), 2.88 - 2.77 (m, 1H), 1.64 - 1.36(m, 11H), 1.33 - 1.26 (m, 6H), 0.95-0.87 (m, 15H); 13C NMR (100 MHz, CDCl3): δ 81.1, 62.5, 52.6,29.3, 27.5, 27.2, 13.9, 10.7, 9.2; Rf = 0.12 (EtOAc); ESI-HRMS calcd for C17H40N1O1Sn1 [M + H]+394.2126, found 394.2122.

Reference： [1]Synlett,2019,vol. 30,p. 464 - 470

18
[ 5077-67-8 ]
[ 100-46-9 ]
[ 96-20-8 ]
[ 100-52-7 ]

Reference： [1]ChemCatChem,2019,vol. 11,p. 3287 - 3295

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Ghs Precautionary Statements

Precautionary Statements-General
Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
P210	Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
P211	Do not spray on an open flame or other ignition source.
P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
P271	Use only outdoors or in a well-ventilated area.
P272	Contaminated work clothing should not be allowed out of the workplace.
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P280	Wear protective gloves/protective clothing/eye protection/face protection.
P281	Use personal protective equipment as required.
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P231 + P232	Handle under inert gas. Protect from moisture.
P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
P304	IF INHALED:
P305	IF IN EYES:
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P312	Call a POISON CENTER or doctor/physician if you feel unwell.
P313	Get medical advice/attention.
P314	Get medical advice/attention if you feel unwell.
P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
P331	Do NOT induce vomiting.
P332	IF SKIN irritation occurs:
P333	If skin irritation or rash occurs:
P334	Immerse in cool water/wrap n wet bandages.
P335	Brush off loose particles from skin.
P336	Thaw frosted parts with lukewarm water. Do not rub affected area.
P337	If eye irritation persists:
P338	Remove contact lenses, if present and easy to do. Continue rinsing.
P340	Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
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P362	Take off contaminated clothing and wash before reuse.
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P370	In case of fire:
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P373	DO NOT fight fire when fire reaches explosives.
P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
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P378
P380	Evacuate area.
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P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
P370 + P380	In case of fire: Evacuate area.
P370 + P380 + P375	In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
Storage
Code	Phrase
P401
P402	Store in a dry place.
P403	Store in a well-ventilated place.
P404	Store in a closed container.
P405	Store locked up.
P406	Store in corrosive resistant/ container with a resistant inner liner.
P407	Maintain air gap between stacks/pallets.
P410	Protect from sunlight.
P411
P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Purity	Size	Price	VIP Price	USA Stock *0-1 Day	Global Stock *5-7 Days	Quantity
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Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

[ CAS No. 96-20-8 ] {[proInfo.proName]}

Quality Control of [ 96-20-8 ]

Related Doc. of [ 96-20-8 ]

Product Details of [ 96-20-8 ]

Safety of [ 96-20-8 ]

Application In Synthesis of [ 96-20-8 ]

[ 96-20-8 ] Synthesis Path-Upstream 1~16

[ 96-20-8 ] Synthesis Path-Downstream 1~18

Related Functional Groups of [ 96-20-8 ]

Aliphatic Chain Hydrocarbons

Alcohols

Amines

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Related Functional Groups of
[ 96-20-8 ]