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Alcohols and polyols

Organic compounds containing one or more hydroxyl functional groups bonded to a carbon atom; hydroxyls consist of an oxygen atom bonded to a hydrogen atom. Alcohols exist in chain, or as closed rings. Polyols contain two or more hydroxyl groups.
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1

Monocaprin 98.0+%, TCI America™

CAS: 26402-22-2 Molecular Formula: C13H26O4 Molecular Weight (g/mol): 246.35 MDL Number: MFCD00056656 InChI Key: LKUNXBRZDFMZOK-UHFFFAOYNA-N Synonym: Glycerol alpha-Monodecanoate, 1-Monodecanoyl Glycerol PubChem CID: 92926 ChEBI: CHEBI:75551 IUPAC Name: 2,3-dihydroxypropyl decanoate SMILES: CCCCCCCCCC(=O)OCC(O)CO

PubChem CID 92926
CAS 26402-22-2
Molecular Weight (g/mol) 246.35
ChEBI CHEBI:75551
MDL Number MFCD00056656
SMILES CCCCCCCCCC(=O)OCC(O)CO
Synonym Glycerol alpha-Monodecanoate, 1-Monodecanoyl Glycerol
IUPAC Name 2,3-dihydroxypropyl decanoate
InChI Key LKUNXBRZDFMZOK-UHFFFAOYNA-N
Molecular Formula C13H26O4
2

Polyethylene Glycol Monostearate (n=approx. 55) (palmitate and stearate mixture), TCI America™

CAS: 9004-99-3 Molecular Formula: C20H40O3 Molecular Weight (g/mol): 328.537 MDL Number: MFCD00148007 InChI Key: RFVNOJDQRGSOEL-UHFFFAOYSA-N PubChem CID: 24762 IUPAC Name: 2-hydroxyethyl octadecanoate SMILES: CCCCCCCCCCCCCCCCCC(=O)OCCO

PubChem CID 24762
CAS 9004-99-3
Molecular Weight (g/mol) 328.537
MDL Number MFCD00148007
SMILES CCCCCCCCCCCCCCCCCC(=O)OCCO
IUPAC Name 2-hydroxyethyl octadecanoate
InChI Key RFVNOJDQRGSOEL-UHFFFAOYSA-N
Molecular Formula C20H40O3
3

5-Norbornene-2-exo,3-exo-dimethanol 97.0+%, TCI America™

CAS: 699-95-6 Molecular Formula: C9H14O2 Molecular Weight (g/mol): 154.209 InChI Key: IGHHPVIMEQGKNE-ROVKLQMOSA-N Synonym: bicyclo 2.2.1 hept-5-ene-2-exo,3-exo-dimethanol PubChem CID: 73995587 IUPAC Name: [(1R,3S,4S)-3-(hydroxymethyl)-2-bicyclo[2.2.1]hept-5-enyl]methanol SMILES: C1C2C=CC1C(C2CO)CO

PubChem CID 73995587
CAS 699-95-6
Molecular Weight (g/mol) 154.209
SMILES C1C2C=CC1C(C2CO)CO
Synonym bicyclo 2.2.1 hept-5-ene-2-exo,3-exo-dimethanol
IUPAC Name [(1R,3S,4S)-3-(hydroxymethyl)-2-bicyclo[2.2.1]hept-5-enyl]methanol
InChI Key IGHHPVIMEQGKNE-ROVKLQMOSA-N
Molecular Formula C9H14O2
4
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2-Phenyl-1,3-propanediol, 98%

CAS: 1570-95-2 Molecular Formula: C9H12O2 Molecular Weight (g/mol): 152.193 MDL Number: MFCD00236056 InChI Key: BPBDZXFJDMJLIB-UHFFFAOYSA-N Synonym: 2-phenyl-1,3-propanediol,2-phenyl-1,3-propanediole,2-phenyl-propane-1,3-diol,2-phenyl-1,3-propane diol,unii-9f93674jbb,1,3-propanediol, 2-phenyl,phenylpropanediol,pubchem20386,rarechem al bd 1370,acmc-1bz5a PubChem CID: 254178 IUPAC Name: 2-phenylpropane-1,3-diol SMILES: C1=CC=C(C=C1)C(CO)CO

PubChem CID 254178
CAS 1570-95-2
Molecular Weight (g/mol) 152.193
MDL Number MFCD00236056
SMILES C1=CC=C(C=C1)C(CO)CO
Synonym 2-phenyl-1,3-propanediol,2-phenyl-1,3-propanediole,2-phenyl-propane-1,3-diol,2-phenyl-1,3-propane diol,unii-9f93674jbb,1,3-propanediol, 2-phenyl,phenylpropanediol,pubchem20386,rarechem al bd 1370,acmc-1bz5a
IUPAC Name 2-phenylpropane-1,3-diol
InChI Key BPBDZXFJDMJLIB-UHFFFAOYSA-N
Molecular Formula C9H12O2
5
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Neopentyl alcohol, 99%

CAS: 75-84-3 Molecular Formula: C5H12O Molecular Weight (g/mol): 88.15 MDL Number: MFCD00004682 InChI Key: KPSSIOMAKSHJJG-UHFFFAOYSA-N Synonym: neopentyl alcohol,2,2-dimethyl-1-propanol,2,2-dimethylpropanol,tert-butylcarbinol,1-propanol, 2,2-dimethyl,tert-butyl carbinol,neopentanol,neopentylalcohol,neoamyl alcohol,2,2-dimethylpropyl alcohol PubChem CID: 6404 IUPAC Name: 2,2-dimethylpropan-1-ol SMILES: CC(C)(C)CO

PubChem CID 6404
CAS 75-84-3
Molecular Weight (g/mol) 88.15
MDL Number MFCD00004682
SMILES CC(C)(C)CO
Synonym neopentyl alcohol,2,2-dimethyl-1-propanol,2,2-dimethylpropanol,tert-butylcarbinol,1-propanol, 2,2-dimethyl,tert-butyl carbinol,neopentanol,neopentylalcohol,neoamyl alcohol,2,2-dimethylpropyl alcohol
IUPAC Name 2,2-dimethylpropan-1-ol
InChI Key KPSSIOMAKSHJJG-UHFFFAOYSA-N
Molecular Formula C5H12O
6

Medchemexpress LLC 2-(2-Phenylethyl)chromone | 61828-53-3 | 50 MG
SDP

2-(2-Phenylethyl)chromone (Flidersiachromone) is a chromone derivative and antioxidant. It scavenges ABTS·+ free radicals, and its derivatives show various activities, including anti-inflammatory, neuroprotective, anti-tumor, and α-glucosidase inhibitory effects. This product is suitable for experimental research in areas such as inflammation-related diseases, tumors, and neurodegenerative diseases.

  • Chromone derivative and antioxidant
  • Scavenges ABTS·+ free radicals
  • Derivatives exhibit diverse activities, such as anti-inflammatory, neuroprotective, anti-tumor, and α-glucosidase inhibitory effects
  • Applicable for experimental research in inflammation-related diseases, tumors, and neurodegenerative diseases
  • Purity: 99.94%
  • Derivatives show α-glucosidase inhibitory activity
  • Derivatives demonstrate neuroprotective activity by protecting human neuroblastoma SH-SY5Y cells against H2O2-induced apoptosis

ENCOMPASS_PREFERRED
7

Medchemexpress LLC 2-(2-Phenylethyl)chromone (Flidersiachromone) | 61828-53-3 | 100 MG
SDP

2-(2-Phenylethyl)chromone (Flidersiachromone) is a chromone derivative that functions as an antioxidant. It is capable of scavenging ABTS·+ free radicals. Derivatives of this compound have demonstrated a range of activities, including anti-inflammatory, neuroprotective, anti-tumor, and α-glucosidase inhibitory effects. It is suitable for experimental research in areas such as inflammation-related diseases, tumors, and neurodegenerative diseases.

  • Chromone derivative.
  • Acts as an antioxidant agent.
  • Scavenges ABTS·+ free radicals.
  • Derivatives exhibit anti-inflammatory effects.
  • Derivatives exhibit neuroprotective effects.
  • Derivatives exhibit anti-tumor effects.
  • Derivatives show α-glucosidase inhibitory effects.
  • Applicable to research in inflammation-related diseases.
  • Applicable to research in tumors.
  • Applicable to research in neurodegenerative diseases.

ENCOMPASS_PREFERRED
8

Medchemexpress LLC 4H-1-Benzopyran-4-one, 2-(2-phenylethyl)- | 61828-53-3 | 25 MG
SDP

2-(2-Phenylethyl) chromone (Flidersiachromone) is a chromone derivative and an antioxidant. It scavenges ABTS·+ free radicals, and its derivatives show various activities such as anti-inflammatory, neuroprotective, anti-tumor, and α-glucosidase inhibitory effects. This product is suitable for experimental research in areas like inflammation-related diseases, tumors, and neurodegenerative diseases.

  • Chromone derivative and antioxidant
  • Scavenges ABTS·+ free radicals
  • Exhibits anti-inflammatory activity
  • Exhibits neuroprotective activity
  • Exhibits anti-tumor activity
  • Exhibits α-glucosidase inhibitory effects
  • Suitable for research in inflammation-related diseases
  • Suitable for research in tumors
  • Suitable for research in neurodegenerative diseases

ENCOMPASS_PREFERRED
9

Sigma Aldrich Fine Chemicals Biosciences 2-Mercaptoethanol-1,1,2,2-d4 98 atom % D, 98% (CP) | 284474-53-9 | MFCD00142936 | 250MG

2-Mercaptoethanol-1,1,2,2-d4 98 atom % D, 98% (CP) | Purity: 98% (CP) | Mol Wt: 82.16 | 284474-53-9 | MFCD00142936 | 250MG

ENCOMPASS
10

eMolecules​ 2602564-53-2 | (1H-Indazol-7-yl)-hydrazine hydrochloride | J&W PharmLab LLC184.630 | C7H9ClN4 | 96.000 | Cl.NNc1cccc2cn[nH]c12 | 1g | 571062602

(1H-Indazol-7-yl)-hydrazine hydrochloride | J&W PharmLab LLC | 2602564-53-2184.630 | C7H9ClN4 | 96.000 | Cl.NNc1cccc2cn[nH]c12 | 1g | 571062602

ENCOMPASS_PREFERRED
11

eMolecules​ 83948-53-2 | tert-butyl N-(3-bromopropyl)carbamate | Pharmablock | MFCD02683429 | 238.125 | C8H16BrNO2 | 97.000 | CC(C)(C)OC(=O)NCCCBr | 2.5g | 686930300

tert-butyl N-(3-bromopropyl)carbamate | Pharmablock | 83948-53-2 | MFCD02683429 | 238.125 | C8H16BrNO2 | 97.000 | CC(C)(C)OC(=O)NCCCBr | 2.5g | 686930300

ENCOMPASS_PREFERRED
12

eMolecules​ 422509-53-3 | (11bS)-N-(1-Phenylethyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine | ChemScene | MFCD19703258 | 435.463 | C28H22NO2P | 95.000 | CC(NP1Oc2ccc3ccccc3c2-c2c(O1)ccc1ccccc21)c1ccccc1 | 250mg | 837434168

(11bS)-N-(1-Phenylethyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine | ChemScene | 422509-53-3 | MFCD19703258 | 435.463 | C28H22NO2P | 95.000 | CC(NP1Oc2ccc3ccccc3c2-c2c(O1)ccc1ccccc21)c1ccccc1 | 250mg | 837434168

ENCOMPASS_PREFERRED
13

eMolecules​ 422509-53-3 | (11bS)-N-(1-Phenylethyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine | ChemScene | MFCD19703258 | 435.463 | C28H22NO2P | 95.000 | CC(NP1Oc2ccc3ccccc3c2-c2c(O1)ccc1ccccc21)c1ccccc1 | 500mg | 601110628

(11bS)-N-(1-Phenylethyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine | ChemScene | 422509-53-3 | MFCD19703258 | 435.463 | C28H22NO2P | 95.000 | CC(NP1Oc2ccc3ccccc3c2-c2c(O1)ccc1ccccc21)c1ccccc1 | 500mg | 601110628

ENCOMPASS_PREFERRED
14

eMolecules​ 194799-53-6 | 3-(3-Aminophenyl)-2-ethyl-1-phenyl-3-pyrazolin-5-one | Combi-Blocks, Inc. | MFCD00020797 | 279.343 | C17H17N3O | 95.000 | CCn1c(cc(=O)n1-c1ccccc1)-c1cccc(N)c1 | 250mg | 603152863

3-(3-Aminophenyl)-2-ethyl-1-phenyl-3-pyrazolin-5-one | Combi-Blocks, Inc. | 194799-53-6 | MFCD00020797 | 279.343 | C17H17N3O | 95.000 | CCn1c(cc(=O)n1-c1ccccc1)-c1cccc(N)c1 | 250mg | 603152863

ENCOMPASS_PREFERRED
15

eMolecules​ 471-53-4 | Enoxolone | Oakwood Chemicals470.694 | C30H46O4 | 97.000 | CC1(C)[C@@H](O)CC[C@@]2(C)C1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O | 1g | 480165054

Enoxolone | Oakwood Chemicals | 471-53-4470.694 | C30H46O4 | 97.000 | CC1(C)[C@@H](O)CC[C@@]2(C)C1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O | 1g | 480165054

ENCOMPASS_PREFERRED