3-Phosphoglyceraldehyde

HCID 729CAS 591-59-3

Basic information

Standard SMILES
O=CC(O)COP(=O)(O)O
InChIKey
LXJXRIRHZLFYRP-UHFFFAOYSA-N
Molecular formula
C3H7O6P
Average molar mass
170.06 g/mol
Monoisotopic mass
169.99802494

Names & identifiers

Preferred name
3-Phosphoglyceraldehyde
IUPAC
(2-hydroxy-3-oxopropyl) dihydrogen phosphate
English name
DL-Glyceraldehyde 3-phosphate
Molecular formula
C3H7O6P
Molecular weight
170.06

Names & synonyms

DL-Glyceraldehyde 3-phosphate591-59-33-phosphoglyceraldehyde(2-hydroxy-3-oxopropyl) dihydrogen phosphateEINECS 209-721-77466PL1110DTXSID80349247RefChem:505003DTXCID40300319209-721-710030-19-0GLYCERALDEHYDE 3-PHOSPHATE
Show more names
5G1000g,5kgLXJXRIRHZLFYRP-UHFFFAOYSA-NPropal,2-hydroxy-3-(phosphonooxy)-DL-GLYCERALDEHYDE 3-PHOSPHATE FREE Adl-glyceraldehyde 3-phosphate solutiondl-glyceraldehyde 3-phosphate free acidDL-Glyceraldehyde 3-Phosphate DISCONTINUED.
glyceraldehyde-3-phosphate142-10-92-hydroxy-3-(phosphonooxy)propanal2-hydroxy-3-oxopropyl dihydrogen phosphateGlycerinaldehyd-3-phosphatPropanal, 2-hydroxy-3-(phosphonooxy)-DL-Glyceraldehyde 3-phosphate - 45-55 mg/mL aqueous solutionDTXSID40861814

Database identifiers

CAS
591-59-3
PubChem CID
729
DTXSID
DTXSID40861814
ChEBI
CHEBI:17138
UNII
7466PL1110
EC Number
209-721-7
Nikkaji
J228.059K

Properties

Computed structural properties

XLogP
-2.7
Topological polar surface area
104 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
6
Rotatable bonds
4
Heavy atoms
10

Physicochemical properties

Boiling point
399.2 · 399.2±52.0 °C(Predicted)
Density
1.721 · 1.721±0.06 g/cm3(Predicted)
storage temp.
-20 °C · -20°C
solubility
50 mg/ml · Water: 50 mg/ml
pka
1.8 · 1.80±0.10(Predicted)
form
Liquid

Safety & regulation

GHS classification

GHS Classification · 5 items

Danger

H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation];H318 (97.4%): Causes serious eye damage [Danger Serious eye damage/eye irritation]

P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P363, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

Hazard information

Hazard Classes and CategoriesSkin Corr. 1B (100%);Eye Dam. 1 (97.4%)

Safety data

PPE
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
wgk
3
ridadr
UN 1760 8/PG 2
risk_code
34
Signal word
Danger
Symbol(GHS)
GHS05

Chemistry & industry

Applications · 2 items

DescriptionDL-Glyceraldehyde-3-phosphate (GADP) is an intermediate in several metabolic pathways, including glycolysis and gluconeogenesis. In glycolysis, it can be derived from fructose 1,6-bisphosphate by fructose bisphosphate aldolase in a reaction that also produces dihydroxyacetone phosphate (DHAP). Triose phosphate isomerase reversibly converts DHAP to GADP. GADP is processed to 1,3-bisphosphoglycerate by glyceraldehyde phosphate dehydrogenase and NAD+.

UsesThe level of Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) activity in HEK 293 cells was aβeβed by measuring the reduction of NAD+ by DL-Glyceraldehyde 3-phosphate.

Suppliers29 total

Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
广州佳途科技股份有限公司81960175 18933936954 · [email protected]
杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
江苏星科元信息科技有限公司400-605-7200 15335295587
江苏艾康生物医药研发有限公司025-025-66113011 15955137747 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Glyceraldehyde 3-phosphate is an aldotriose phosphate that is the 3-phospho derivative of glyceraldehyde. It is an important metabolic intermediate in several central metabolic pathways in all organisms. It has a role as a human metabolite, a plant metabolite and an Escherichia coli metabolite. It is an aldotriose phosphate and an aldehyde. It is functionally related to a glyceraldehyde. It is a conjugate acid of a glyceraldehyde 3-phosphate(2-).

Related reactions

1 records

Linked notes

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